US20220073944A1

US20220073944A1 - Multimeric coding nucleic acid and uses thereof

Info

Publication number: US20220073944A1
Application number: US17/404,283
Authority: US
Inventors: Frank DeRosa; Michael Heartlein; Daniel CRAWFORD; Shrirang Karve
Original assignee: Translate Bio Inc; RaNA Therapeutics Inc
Current assignee: Translate Bio Inc
Priority date: 2016-04-08
Filing date: 2021-08-17
Publication date: 2022-03-10
Also published as: US20170314041A1; US11124804B2; EP3440206A1; AU2021206908A1; CA3020343A1; EP3440206B1; JP7150608B2; CN109072223A; AU2017248189B2; JP2019513372A; ES2844180T3; KR102475301B1; DK3440206T3; CN109072223B; KR20190027353A; WO2017177169A1; US20200172923A1; KR20220031741A; US20190249191A1; JP7150608B6

Abstract

The present invention provides, among other things, multimeric coding nucleic acids that exhibit superior stability for in vivo and in vitro use. In some embodiments, a multimeric coding nucleic acid (MCNA) comprises two or more encoding polynucleotides linked via 3′ ends such that the multimeric coding nucleic acid compound comprises two or more 5′ ends.

Description

RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/540,791, filed Aug. 14, 2019, which is a divisional of U.S. application Ser. No. 16/280,772, filed Feb. 20, 2019 and issued as U.S. Pat. No. 10,428,349 on Oct. 1, 2019, which is a divisional of U.S. application Ser. No. 15/482,431, filed Apr. 7, 2017 and issued as U.S. Pat. No. 10,266,843 on Apr. 23, 2019, which claims priority to U.S. Provisional Application No. 62/320,073, filed Apr. 8, 2016, the disclosure of which is hereby incorporated by reference.

SEQUENCE LISTING

The present specification makes reference to a Sequence Listing (submitted electronically as a .txt file named “MRT_1237US4_SL”. The .txt file was generated Aug. 17, 2021 and is 49,367 bytes in size. The entire contents of the Sequence Listing are herein incorporated by reference.

BACKGROUND

Nucleic acid-based technologies are increasingly important for various therapeutic applications including, but not limited to, messenger RNA therapy, gene therapy, and gene editing, to name but a few. Such therapeutic applications typically require administration of exogenous polynucleotides (e.g. DNA or RNA), which is often hampered by the limited stability of such polynucleotides. For example, following their administration to a subject, many polynucleotides may be subject to nuclease (e.g. exonuclease and/or endonuclease) degradation. Nuclease degradation may negatively influence the capability of a polynucleotide to reach a target cell or to be transcribed and/or translated, the result of which is to preclude the exogenous polynucleotide from exerting an intended therapeutic effect.

SUMMARY OF THE INVENTION

The present invention provides, among other things, multimeric coding nucleic acids that exhibit superior stability for in vivo and in vitro use. The present invention also permits increased complexity and efficiency for nucleic acid based therapeutics.
In some aspects, the present invention provides a multimeric coding nucleic acid (MCNA) comprising one or more coding polynucleotides linked to one or more non-coding polynucleotides via a 3′ end linkage between two or more of the polynucleotides (coding or non-coding) such that the MCNA compound comprises two or more 5′ ends. In some embodiments, one or more of the 5′ends is modified to include a 5′ end cap structure. In certain embodiments, one or more of the coding polynucleotides having a 5′ end comprises a 5′ end cap structure to facilitate translation of the coding polynucleotides. In certain embodiments, one or more of the polynucleotides having a 5′end structure comprises a 5′ end cap structure to facilitate stability of the MCNA.
In some aspects, the present invention provides a multimeric coding nucleic acid (MCNA) comprising two or more encoding polynucleotides linked via 3′ ends such that the multimeric coding nucleic acid compound comprises two or more 5′ ends. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polydeoxyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polydeoxyribonucleotide or a polyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides encodes a protein of interest. In some embodiments, each of the two or more encoding polynucleotides encodes a same protein. In some embodiments, each of the two or more encoding polynucleotides encodes a distinct protein.
In some embodiments, the MCNA compound comprises three or more encoding polynucleotides. In some embodiments, the compound comprises four or more encoding polynucleotides. In some embodiments, the compound comprises five or more encoding polynucleotides.
In some embodiments, one or more of the encoding polynucleotides comprise a 5′ untranslated region (5′ UTR) and/or a 3′ untranslated region (3′ UTR). In some embodiments, the one or more of the encoding polynucleotides comprise a 3′ UTR. In some embodiments, the 3′ UTR is 5-2,000 nucleotides in length. In some embodiments, the 3′ UTR comprises a plurality of multi-A segments with spacers in between. In some embodiments, each of the multi-A segments comprises 8-50 consecutive adenosines. In some embodiments, the plurality of multi-A segments range from 1-100. In some embodiments, the spacers are of varying lengths ranging from 5-100. In some embodiments, the spacers comprise DNA, RNA and/or modified bases. In some embodiments, the modified bases are selected from 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ΨU), and 1-methyl-pseudouridine. In some embodiments, the 3′ UTR comprises a pseudoknot structure. In some embodiments, the 3′ UTR is not followed with a polyadenylation (poly-A) tail. In some embodiments, one or more of the encoding polynucleotides comprise a poly-A tail. In some embodiments, the poly-A tail is 25-5,000 nucleotides in length. In some embodiments, the 3′ UTR binds to poly-A binding proteins (PABPs). In some embodiments, the 3′ UTR comprises a “kissing loop” sequence motif.
In some embodiments, the 3′ ends of the two or more encoding polynucleotides are linked via an oligonucleotide bridge comprising a 3′-3′ inverted phosphodiester linkage. In some embodiments, the nucleotides comprising the oligonucleotide bridge are selected from the group consisting of 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ΨU), and 1-methyl-pseudouridine. In some embodiments, the oligonucleotide bridge comprises at least one covalent link to an active moiety. In some embodiments, the active moiety is a targeting group, peptide, contrast agent, small molecule, protein, DNA and/or RNA. In some embodiments, nucleotides proximal to the 3′-3′ inverted linkage are functionalized with one or more tri-antennary GalNac targeting agents.
In some embodiments, the encoding polynucleotides comprise one or more modified nucleotides. In some embodiments, the modified nucleotides are selected from the group consisting of 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ΨU), and 1-methyl-pseudouridine. In some embodiments, the modified nucleotides substitute 1-100% of corresponding native bases. In some embodiments, the at least 25% of uridines are replaced with 2-thiouridines. In some embodiments, 100% of cytidines are replaced with 5-methylcytidines. In some embodiments, the modified nucleotides are further modified with a 4′-thio substitution on the ribose ring. In some embodiments, the native nucleotides are modified with a 4′-thio substitution on the ribose ring.
In some embodiments, one or more encoding polynucleotides in the MCNA comprise a polynucleotide portion that encodes a therapeutic protein. In some embodiments, one or more encoding polynucleotides in the MCNA comprise a polynucleotide portion that encodes an enzyme, a receptor, a ligand, a light chain or heavy chain of an antibody, a nuclease, or a DNA-binding protein. In certain embodiments, one or more encoding polynucleotides in the MCNA comprise a polynucleotide portion that encodes a nuclease.
In some embodiments, the two or more encoding polynucleotides in the MCNA each comprise a polynucleotide portion that encodes a therapeutic protein. In some embodiments, the two or more encoding polynucleotides in the MCNA each comprise a polynucleotide portion that encodes an enzyme, a receptor, a ligand, a light chain or heavy chain of an antibody, a nuclease, and/or a DNA-binding protein. In some embodiments, the two or more encoding polynucleotides in the MCNA each comprise a polynucleotide portion that encodes a nuclease.
In some embodiments, a first encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a first protein and a second encoding polynucleotide in the MCNA comprising a polynucleotide portion that encodes a second protein that is the same protein as the first protein. In some embodiments, a first encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a first protein and a second encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a second protein that is distinct from the first protein. In certain embodiments, a first encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a first protein in a class of an enzyme, a receptor, a ligand, a light chain or heavy chain of an antibody, a nuclease, or a DNA-binding protein, and a second encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a second protein that is distinct from the first protein but in the same class as the first protein. In certain embodiments, a first encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a first protein in a class of an enzyme, a receptor, a ligand, a light chain or heavy chain of an antibody, a nuclease, or a DNA-binding protein, and a second encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a second protein that is distinct from the first protein and in a different class from the first protein. In certain embodiments, a first encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a light chain of an antibody and a second encoding polynucleotide in the MCNA comprises a polynucleotide portion that encodes a heavy chain in the antibody.
In some aspects, the present invention provides a multimeric nucleic acid (MNA) comprising two or more polynucleotides linked via at least one 3′ end linkage between two or more of the polynucleotides such that the MNA compound comprises two or more 5′ ends. In some embodiments, one or more of the 5′ ends is modified to facilitate stability of the MNA. In certain embodiments, the two or more polynucleotides linked via the at least one 3′ end linkage each are non-coding nucleotides.
In some aspects, the present invention provides a composition comprising the MCNA as described above, encapsulated or complexed with a delivery vehicle. In some embodiments, the delivery vehicle is selected from the group consisting of liposomes, lipid nanoparticles, solid-lipid nanoparticles, polymers, viruses, sol-gels, and nanogels.
In some aspects, the present invention provides methods of delivering MCNA for in vivo protein production, comprising administering the MCNA as described above to a subject in need of delivery. In some embodiments, the MCNA is administered via a route of delivery selected from the group consisting of intravenous delivery, subcutaneous delivery, oral delivery, subdermal delivery, ocular delivery, intratracheal injection pulmonary delivery (e.g. nebulization), intramuscular delivery, intrathecal delivery, or intraarticular delivery.
It is to be understood that all embodiments as described above are applicable to all aspects of the present invention.

BRIEF DESCRIPTION OF THE DRAWING

The drawings are for illustration purposes only, not for limitation.

FIG. 1 shows an exemplary MCNA comprising two RNA species linked via a 3′-3′ inverted RNA nucleotide dimer.

FIG. 2 shows an exemplary MCNA comprising two RNA species linked via a 3′-3′ inverted RNA nucleotide dimer wherein the MCNA is functionalized with a tri-antennary GalNac targeting agent.

FIG. 3 shows an exemplary MCNA comprising two RNA species linked via a 3′-3′ inverted RNA nucleotide dimer wherein the MCNA is functionalized with two tri-antennary GalNac targeting agent.

FIG. 4 shows a general scheme for synthesis of MCNA.

FIG. 5 shows exemplary results of synthesized EPO MCNA detected via gel electrophoresis. Constructs were synthesized under the following conditions: RNA Ligase 1 (A); RNA Ligase 1+10% PEG (B); and RNA Ligase 2 (C).

FIG. 6 shows exemplary results of synthesized EPO MCNA detected via gel electrophoresis. Lane 1 show capped EPO RNA with no tail. Lane 2 shows an EPO MCNA mixture with no DNAse treatment. Lane 3 shows an EPO MCNA mixture treated with DNAse.

FIG. 7 shows an exemplary graph of the level of hEPO protein secreted after transfection of HEK293T cells with synthetic constructs comprising untailed EPO mRNA or MCNA comprising hEPO mRNA (1 microgram per construct).

FIG. 8 shows exemplary results of synthesized EPO MCNA detected via gel electrophoresis. Lane 1 contains an RNA Ladder, Lane 2 contains a ligation product for EPO MCNA that was not purified, Lane 3 contains purified unreacted/partially reacted product and Lane 4 contains purified EPO MCNA ligation product.

FIG. 9 shows an exemplary graph of the level of hEPO protein secreted after transfection of HEK293T cells with synthetic constructs comprising untailed EPO mRNA or purified MCNA comprising hEPO mRNA (250 nanogram per construct).

FIG. 10 shows an exemplary graph of the level of hOTC protein activity measured in cell lysate after transfection of HEK293T cells with synthetic constructs comprising untailed hOTC mRNA (hOTC monomer) or MCNA comprising hOTC mRNA.

FIG. 11 shows an exemplary graph of the level of hPAH protein produced after transfection of HEK293T cells with synthetic constructs comprising untailed hPAH mRNA (hPAH monomer) or MCNA comprising hPAH mRNA.

FIG. 12 shows an exemplary Western blot demonstrating hCFTR protein production after transfection of HEK293T cells with synthetic constructs comprising untailed hCFTR mRNA (hCFTR monomer) or MCNA comprising hCFTR mRNA.

FIG. 13 shows an exemplary graph of citrulline production measured in livers of mice after treatment with hOTC MCNA encapsulated in lipid nanoparticles.

FIG. 14 shows an exemplary Western blot demonstrating hOTC production detected in livers of mice after treatment with hOTC MCNA or hOTC monomers encapsulated in lipid nanoparticles.

FIG. 15 shows an exemplary graph of citrulline production measured in livers of mice after treatment with hOTC mRNA encapsulated in lipid nanoparticles.

FIG. 16 shows an exemplary graph comparing citrulline production 1 week after administration as a percentage of citrulline production 24 hours after administration in mice treated with hOTC mRNA or hOTC MCNA encapsulated in lipid nanoparticles.

FIG. 17 shows an exemplary graph of hPAH protein detected in livers of PAH knock-out (KO) mice 24 hours after they were administered either hPAH MCNA or hPAH monomers encapsulated in lipid nanoparticles.

FIG. 18 shows an exemplary graph of serum phenylalanine levels in PAH knock-out (KO) mice 24 hours after they were administered either hPAH MCNA or hPAH monomers encapsulated in lipid nanoparticles.

FIG. 19 shows an exemplary graph of hEPO protein detected in the serum of wild-type mice 24 hours after they were administered either hEPO MCNA or hEPO monomers encapsulated in lipid nanoparticles.

FIG. 20 shows exemplary immunohistochemical detection of human Cystic Fibrosis Transmembrane Conductance Regulator (hCFTR) protein in CFTR KO mouse lung 24 hours and 7 days after treatment with hCFTR MCNA encapsulated in lipid nanoparticles via aerosolization.

DEFINITIONS

In order for the present invention to be more readily understood, certain terms are first defined below. Additional definitions for the following terms and other terms are set forth throughout the specification. The publications and other reference materials referenced herein to describe the background of the invention and to provide additional detail regarding its practice are hereby incorporated by reference.
Amino acid: As used herein, the term “amino acid,” in its broadest sense, refers to any compound and/or substance that can be incorporated into a polypeptide chain. In some embodiments, an amino acid has the general structure H2N—C(H)(R)—COOH. In some embodiments, an amino acid is a naturally occurring amino acid. In some embodiments, an amino acid is a synthetic amino acid; in some embodiments, an amino acid is a d-amino acid; in some embodiments, an amino acid is an 1-amino acid. “Standard amino acid” refers to any of the twenty standard 1-amino acids commonly found in naturally occurring peptides. “Nonstandard amino acid” refers to any amino acid, other than the standard amino acids, regardless of whether it is prepared synthetically or obtained from a natural source. As used herein, “synthetic amino acid” encompasses chemically modified amino acids, including but not limited to salts, amino acid derivatives (such as amides), and/or substitutions. Amino acids, including carboxy- and/or amino-terminal amino acids in peptides, can be modified by methylation, amidation, acetylation, protecting groups, and/or substitution with other chemical groups that can change the peptide's circulating half-life without adversely affecting their activity. Amino acids may participate in a disulfide bond. Amino acids may comprise one or posttranslational modifications, such as association with one or more chemical entities (e.g., methyl groups, acetate groups, acetyl groups, phosphate groups, formyl moieties, isoprenoid groups, sulfate groups, polyethylene glycol moieties, lipid moieties, carbohydrate moieties, biotin moieties, etc.). The term “amino acid” is used interchangeably with “amino acid residue,” and may refer to a free amino acid and/or to an amino acid residue of a peptide. It will be apparent from the context in which the term is used whether it refers to a free amino acid or a residue of a peptide.
Animal: As used herein, the term “animal” refers to any member of the animal kingdom. In some embodiments, “animal” refers to humans, at any stage of development. In some embodiments, “animal” refers to non-human animals, at any stage of development. In certain embodiments, the non-human animal is a mammal (e.g., a rodent, a mouse, a rat, a rabbit, a monkey, a dog, a cat, a sheep, cattle, a primate, and/or a pig). In some embodiments, animals include, but are not limited to, mammals, birds, reptiles, amphibians, fish, insects, and/or worms. In some embodiments, an animal may be a transgenic animal, genetically-engineered animal, and/or a clone.
Approximately or about: As used herein, the term “approximately” or “about,” as applied to one or more values of interest, refers to a value that is similar to a stated reference value. In certain embodiments, the term “approximately” or “about” refers to a range of values that fall within 25%, 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or less in either direction (greater than or less than) of the stated reference value unless otherwise stated or otherwise evident from the context (except where such number would exceed 100% of a possible value).
Biologically active: As used herein, the term “biologically active” refers to a characteristic of any agent that has activity in a biological system, and particularly in an organism. For instance, an agent that, when administered to an organism, has a biological effect on that organism, is considered to be biologically active.
Delivery: As used herein, the term “delivery” encompasses both local and systemic delivery. For example, delivery of MCNA encompasses situations in which an MCNA is delivered to a target tissue and the encoded protein is expressed and retained within the target tissue (also referred to as “local distribution” or “local delivery”), and situations in which an MCNA is delivered to a target tissue and the encoded protein is expressed and secreted into patient's circulation system (e.g., serum) and systematically distributed and taken up by other tissues (also referred to as “systemic distribution” or “systemic delivery).
Expression: As used herein, “expression” of a nucleic acid sequence refers to translation of an MCNA into a polypeptide, assemble multiple polypeptides into an intact protein (e.g., enzyme) and/or post-translational modification of a polypeptide or fully assembled protein (e.g., enzyme). In this application, the terms “expression” and “production,” and grammatical equivalent, are used inter-changeably.
Functional: As used herein, a “functional” biological molecule is a biological molecule in a form in which it exhibits a property and/or activity by which it is characterized.
Half-life: As used herein, the term “half-life” is the time required for a quantity such as nucleic acid or protein concentration or activity to fall to half of its value as measured at the beginning of a time period.
Improve, increase, or reduce: As used herein, the terms “improve,” “increase” or “reduce,” or grammatical equivalents, indicate values that are relative to a baseline measurement, such as a measurement in the same individual prior to initiation of the treatment described herein, or a measurement in a control subject (or multiple control subject) in the absence of the treatment described herein. A “control subject” is a subject afflicted with the same form of disease as the subject being treated, who is about the same age as the subject being treated.
In Vitro: As used herein, the term “in vitro” refers to events that occur in an artificial environment, e.g., in a test tube or reaction vessel, in cell culture, etc., rather than within a multi-cellular organism.
In Vivo: As used herein, the term “in vivo” refers to events that occur within a multi-cellular organism, such as a human and a non-human animal. In the context of cell-based systems, the term may be used to refer to events that occur within a living cell (as opposed to, for example, in vitro systems).
Isolated: As used herein, the term “isolated” refers to a substance and/or entity that has been (1) separated from at least some of the components with which it was associated when initially produced (whether in nature and/or in an experimental setting), and/or (2) produced, prepared, and/or manufactured by the hand of man. Isolated substances and/or entities may be separated from about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or more than about 99% of the other components with which they were initially associated. In some embodiments, isolated agents are about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or more than about 99% pure. As used herein, a substance is “pure” if it is substantially free of other components. As used herein, calculation of percent purity of isolated substances and/or entities should not include excipients (e.g., buffer, solvent, water, etc.).
messenger RNA (mRNA): As used herein, the term “messenger RNA (mRNA)” or “mRNA” refers to a polynucleotide that encodes at least one polypeptide. mRNA as used herein encompasses both modified and unmodified RNA. mRNA may contain one or more coding and non-coding regions. mRNA can be purified from natural sources, produced using recombinant expression systems and optionally purified, chemically synthesized, etc. Where appropriate, e.g., in the case of chemically synthesized molecules, mRNA can comprise nucleoside analogs such as analogs having chemically modified bases or sugars, backbone modifications, etc. An mRNA sequence is presented in the 5′ to 3′ direction unless otherwise indicated. A typical mRNA molecule has a 5′ end and a 3′ end. In some embodiments, an mRNA is or comprises natural nucleosides (e.g., adenosine, guanosine, cytidine, uridine); nucleoside analogs (e.g., 2-aminoadenosine, 2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyl adenosine, 5-methylcytidine, C-5 propynyl-cytidine, C-5 propynyl-uridine, 2-aminoadenosine, C5-bromouridine, C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine, C5-propynyl-cytidine, C5-methylcytidine, 2-aminoadenosine, 7-deazaadenosine, 7-deazaguanosine, 8-oxoadenosine, 8-oxoguanosine, O(6)-methylguanine, and 2-thiocytidine); chemically modified bases; biologically modified bases (e.g., methylated bases); intercalated bases; modified sugars (e.g., 2′-fluororibose, ribose, 2′-deoxyribose, arabinose, and hexose); and/or modified phosphate groups (e.g., phosphorothioates and 5′-N-phosphoramidite linkages).
Nucleic acid: As used herein, the term “nucleic acid,” in its broadest sense, refers to any compound and/or substance that is or can be incorporated into a polynucleotide chain. In some embodiments, a nucleic acid is a compound and/or substance that is or can be incorporated into a polynucleotide chain via a phosphodiester linkage. In some embodiments, “nucleic acid” refers to individual nucleic acid residues (e.g., nucleotides and/or nucleosides). In some embodiments, “nucleic acid” refers to a polynucleotide chain comprising individual nucleic acid residues. In some embodiments, “nucleic acid” encompasses RNA as well as single and/or double-stranded DNA and/or cDNA.
Patient: As used herein, the term “patient” or “subject” refers to any organism to which a provided composition may be administered, e.g., for experimental, diagnostic, prophylactic, cosmetic, and/or therapeutic purposes. Typical patients include animals (e.g., mammals such as mice, rats, rabbits, non-human primates, and/or humans). In some embodiments, a patient is a human. A human includes pre- and post-natal forms.
Pharmaceutically acceptable: The term “pharmaceutically acceptable”, as used herein, refers to substances that, within the scope of sound medical judgment, are suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
Pharmaceutically acceptable salt: Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge et al., describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences (1977) 66:1-19. Pharmaceutically acceptable salts of the compounds of this invention include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N⁺(C_1-4alkyl)₄salts. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium. quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, sulfonate and aryl sulfonate. Further pharmaceutically acceptable salts include salts formed from the quaternization of an amine using an appropriate electrophile, e.g., an alkyl halide, to form a quarternized alkylated amino salt.
Systemic distribution or delivery: As used herein, the terms “systemic distribution,” “systemic delivery,” or grammatical equivalent, refer to a delivery or distribution mechanism or approach that affect the entire body or an entire organism. Typically, systemic distribution or delivery is accomplished via body's circulation system, e.g., blood stream. Compared to the definition of “local distribution or delivery.”
Subject: As used herein, the term “subject” refers to a human or any non-human animal (e.g., mouse, rat, rabbit, dog, cat, cattle, swine, sheep, horse or primate). A human includes pre- and post-natal forms. In many embodiments, a subject is a human being. A subject can be a patient, which refers to a human presenting to a medical provider for diagnosis or treatment of a disease. The term “subject” is used herein interchangeably with “individual” or “patient.” A subject can be afflicted with or is susceptible to a disease or disorder but may or may not display symptoms of the disease or disorder.
Substantially: As used herein, the term “substantially” refers to the qualitative condition of exhibiting total or near-total extent or degree of a characteristic or property of interest. One of ordinary skill in the biological arts will understand that biological and chemical phenomena rarely, if ever, go to completion and/or proceed to completeness or achieve or avoid an absolute result. The term “substantially” is therefore used herein to capture the potential lack of completeness inherent in many biological and chemical phenomena.
Target tissues: As used herein, the term “target tissues” refers to any tissue that is affected by a disease to be treated. In some embodiments, target tissues include those tissues that display disease-associated pathology, symptom, or feature.
Therapeutically effective amount: As used herein, the term “therapeutically effective amount” of a therapeutic agent means an amount that is sufficient, when administered to a subject suffering from or susceptible to a disease, disorder, and/or condition, to treat, diagnose, prevent, and/or delay the onset of the symptom(s) of the disease, disorder, and/or condition. It will be appreciated by those of ordinary skill in the art that a therapeutically effective amount is typically administered via a dosing regimen comprising at least one unit dose.
Treating: As used herein, the term “treat,” “treatment,” or “treating” refers to any method used to partially or completely alleviate, ameliorate, relieve, inhibit, prevent, delay onset of, reduce severity of and/or reduce incidence of one or more symptoms or features of a particular disease, disorder, and/or condition. Treatment may be administered to a subject who does not exhibit signs of a disease and/or exhibits only early signs of the disease for the purpose of decreasing the risk of developing pathology associated with the disease.

DETAILED DESCRIPTION

The present invention provides, among other things, methods for synthesizing and compositions comprising multimeric coding nucleic acids (MCNA). In particular, the present invention provides MCNA compounds comprising two or more encoding polynucleotides linked via their 3′ ends such that the MCNA compound comprises two or more 5′ ends and methods of synthesizing the same. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polydeoxyribonucleotide. In some embodiments, a synthetic polyribonucleotide or polydeoxyribonucleotide of the invention codes for a polypeptide, protein, enzyme, antibody, or receptor. In some embodiments, the present invention provides a multimeric nucleic acid (MNA) comprising two or more polynucleotides linked via at least one 3′ end linkage between two or more of the polynucleotides such that the MNA compound comprises two or more 5′ ends. In some embodiments, one or more of the 5′ ends is modified to facilitate stability of the MNA. In certain embodiments, the two or more polynucleotides linked via the at least one 3′ end linkage each are non-coding nucleotides. In some embodiments, a MNA comprises a synthetic polyribonucleotide or polydeoxyribonucleotide that does not code for a polypeptide, protein, enzyme, antibody, or receptor. In some embodiments, MNA comprising a synthetic polyribonucleotide or polydeoxyribonucleotide inhibits gene expression. In some embodiments, a synthetic polyribonucleotide of the invention that inhibits gene expression is a small interfering ribonucleic acid (siRNA), a microRNA (miRNA), or a short hairpin RNA (shRNA).
While the administration of exogenous polynucleotides (e.g. DNA or RNA) represents a meaningful advancement for the treatment of diseases, the administration of such exogenous polynucleotides is often hampered by the limited stability of such polynucleotides, particularly following their in vivo administration. For example, following their administration to a subject, many polynucleotides may be subject to nuclease (e.g. exonuclease and/or endonuclease) degradation. Nuclease degradation may negatively influence the capability of a polynucleotide to reach a target cell or to be transcribed and/or translated, the result of which is to preclude the exogenous polynucleotide from exerting an intended therapeutic effect.
In some embodiments, the MCNA of the present invention exhibit increased in vivo stability compared to a single polynucleotide not linked to another polynucleotide by its 3′ end (hereinafter “monomeric polynucleotide”). In some embodiments, the MCNA of the present invention, when delivered in vivo, lead to enhanced protein production compared to a monomeric polynucleotide encoding the same protein. In some embodiments, the MCNA of the present invention, when delivered to a subject, are tolerated better by the subject compared to a corresponding monomeric polynucleotide.

Multimeric Coding Nucleic Acids (MCNA)

In some embodiments, the present invention provides compositions comprising multimeric coding nucleic acids (MCNA) and methods for synthesizing the same. In particular, the present invention provides MCNA compounds comprising two or more encoding polynucleotides linked via their 3′ ends such that the MCNA compound comprises two or more 5′ ends and methods of synthesizing the same. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polydeoxyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides is a synthetic polydeoxyribonucleotide or a polyribonucleotide. In some embodiments, each of the two or more encoding polynucleotides encodes a protein of interest. In some embodiments, each of the two or more encoding polynucleotides encodes a same protein. In some embodiments, each of the two or more encoding polynucleotides encodes a distinct protein. In some embodiments, each of the two or more encoding polynucleotides encoding a distinct protein are present in equal numbers. In some embodiments, each of the two or more encoding polynucleotides encoding a distinct protein are present in unequal numbers (e.g., 2 copies of a polynucleotide encoding protein of interest # 1 and 1 copy of a polynucleotide encoding protein of interest #2). In some embodiments, a MCNA compound comprises three or more encoding polynucleotides. In some embodiments, a MCNA compound comprises four or more encoding polynucleotides. In some embodiments, a MCNA compound comprises five or more encoding polynucleotides.
In some embodiments, the present invention provides a multimeric nucleic acid (MNA) comprising two or more polynucleotides linked via at least one 3′ end linkage between two or more of the polynucleotides such that the MNA compound comprises two or more 5′ ends. In some embodiments, one or more of the 5′ ends is modified to facilitate stability of the MNA. In certain embodiments, at least one of the two or more polynucleotides linked via the at least one 3′ end linkage is an encoding polynucleotide and at least one of the two or more polynucleotides linked via the at least one 3′ end linkage is a non-coding polynucleotide, thereby constituting a multimeric coding nucleic acid (MCNA). In certain embodiments, the encoding polynucleotide encodes a protein of interest and the non-coding polynucleotide inhibits gene expression (e.g., small interfering ribonucleic acid (siRNA), a microRNA (miRNA), or a short hairpin RNA (shRNA).
In some embodiments, a MCNA compound comprising two or more encoding polynucleotides encodes one or more chains of an antibody or antibody fragment. In some embodiments, the two or more encoding polynucleotides encode a heavy chain and light chain of an antibody. In some embodiments, the antibody is an intact immunoglobulin, (Fab)2, (Fab′)2, Fab, Fab′ or scFv. In some embodiments, the antibody is an IgG. In some embodiments, the antibody is selected from the group consisting of anti-CCL2, anti-lysyl oxidase-like-2 (LOXL2), anti-Flt-1, anti-TNF-α, anti-Interleukin-2Ra receptor (CD25), anti-TGFβ, anti-B-cell activating factor, anti-alpha-4 integrin, anti-BAGE, anti-β-catenin/m, anti-Bcr-abl, anti-CS, anti-CA125, anti-CAMEL, anti-CAP-1, anti-CASP-8, anti-CD4, anti-CD19, anti-CD20, anti-CD22, anti-CD25, anti-CDCl₂7/m, anti-CD 30, anti-CD33, anti-CD52, anti-CD56, anti-CD80, anti-CDK4/m, anti-CEA, anti-CT, anti-CTL4, anti-Cyp-B, anti-DAM, anti-EGFR, anti-ErbB3, anti-ELF2M, anti-EMMPRIN, anti-EpCam, anti-ETV6-AML1, anti-HER2, anti-G250, anti-GAGE, anti-GnT-V, anti-Gp100, anti-HAGE, anti-HER-2/neu, anti-HLA-A*0201-R1701, anti-IGF-1R, anti-IL-2R, anti-IL-S, anti-MC1R, anti-myosin/m, anti-MUC1, anti-MUM-1, -2, -3, anti-proteinase-3, anti-p190 minor bcr-abl, anti-Pml/RARa, anti-PRAMS, anti-PSA, anti-PSM, anti-PSMA, anti-RAGE, anti-RANKL, anti-RU1 or RU2, anti-SAGE, anti-SART-1 or anti-SART-3, anti-survivin, anti-TEL/AML1, anti-TPI/m, anti-TRP-1, anti-TRP-2, anti-TRP-2/INT2, and anti-VEGF or anti-VEGF receptor.
In some embodiments, a MCNA compound comprising two or more encoding polynucleotides encodes one or more nucleases. In some embodiments, each of the one or more nucleases is selected from the group comprising Cas9, zinc-finger nucleases (ZFN), TALEN, homing endonucleases, homing meganucleases, and combinations thereof. Exemplary nucleases include Afu Uracil-DNA Glycosylase (UDG), Tma Endonuclease III, Tth Endonuclease IV, Antarctic Thermolabile UDG, APE 1, Cas9 Nuclease NLS (S. pyogenes), Cas9 Nuclease (S. pyogenes), DNase I, Endonuclease IV, Endonuclease V, Endonuclease VIII, Exonuclease I, Exonuclease III (E. coli), Exonuclease T, Exonuclease V (RecBCD), Exonuclease VII, Exonuclease VIII (truncated), Fpg, hAAG, hOGG1, hSMUG1, Lambda Exonuclease, Micrococcal Nuclease, Mung Bean Nuclease, Nuclease BAL-31, RecA_f, RecJ_f, T4 PDG (T4 Endonuclease V), T5 Exonuclease, T7 Endonuclease I, T7 Exonuclease, Thermostable FEN1, Uracil Glycosylase Inhibitor (UGI). Exemplary homing nucleases include I-AabMI, I-AniI, I-CeuI, I-CkaMI, I-CpaMI, I-CreI, I-DmoI, I-GpeMI, I-GpiI, I-GzeI, I-GzeII, I-HjeMI, I-LtrI, I-LtrWI, I-MpeMI, I-MsoI, I-OnuI, I-PanMI, I-SceI, I-SmaMI, I-Vdi141I, PI-SceI, I-CreI (m), I-MsoI (m), I-OnuI (E2), I-AniI/I-OnuI, I-DmoI/I-CreI, I-GpiI/I-OnuI, I-GzeI/I-PanMI, I-LtrI/I-PanMI, I-OnuI/I-LtrI, I-AaeMIP, I-ApaMIP, I-GzeMIIIP. I-NcrMIP, I-OsoMIIP, I-PanMIIIP, I-PanMIIP, I-ScuMIIIP, I-ScuMIIP, I-ScuMIP, and I-ScuMIVP.
In some embodiments, a MCNA compound comprises two more more polynucleotides that include one, two, or more encoding polynucleotides, wherein each encoding polynucleotide comprises a polynucleotide portion that is an mRNA transcript for a gene and/or for a protein selected from Table 1, Table 2, Table 3, Table 4, Table 5 or Table 6.

TABLE 1

DISEASE/DISORDERS	GENE(S)

Neoplasia	PTEN; ATM; ATR; EGFR; ERBB2; ERBB3; ERBB4; Notch1;
	Notch2; Notch3; Notch4; AKT; AKT2; AKT3; HIF; H1Fla; HIF3a;
	Met; HRG; Bcl2; PPARalpha; PPAR gamma; WT1 (Wilms Tumor);
	FGF Receptor Family members (5 members: 1, 2, 3, 4, 5); CDKN2a;
	APC; RB (retinoblastoma); MEN!; VHL; BRCA1; BRCA2; AR
	(Androgen Receptor); TSG101; IGF; IGF Receptor; Igfl (4
	variants); Igf2 (3 variants); Igfl Receptor; Igf2 Receptor; Bax;
	Bcl2; caspases family (9 members: 1, 2, 3, 4, 6, 7, 8, 9, 12); Kras;
	Apc
Age-related Macular	Aber; Ccl2; Cc2; cp (ceruloplasmin); Timp3; cathepsinD; Vldlr;
Degeneration	Ccr2
Schizophrenia Disorders	Neuregulinl (Nrgl); Erb4 (receptor for Neuregulin); Complexinl
	(Cplxl); Tphl Tryptophan hydroxylase; Tph2 Tryptophan
	hydroxylase 2; Neurexin 1; GSK3; GSK3a; GSK3b; 5-HTT (Slc6a4);
	COMT; DRD (Drdla); SLC6A3; DAOA; DTNBPI; Dao (Dao1)
Trinucleotide Repeat	HTT (Huntington's Dx); SBMA/SMAXI/AR (Kennedy's Dx);
Disorders	FXN/X25 (Friedrich's Ataxia); ATX3 (Machado-Joseph's Dx);
	ATXNI and ATXN2 (spinocerebellar
	ataxias); DMPK (myotonic dystrophy); Atrophin-1 and
	Atn1 (DRPLA Dx); CBP (Creb-BP-global instability); VLDLR
	(Alzheimer's); Atxn7; Atxn10
Fragile X Syndrome	FMR2; FXRI; FXR2; mGLUR5
Secretase Related	APH-1 (alpha and beta); Presenilin (Psen1); nicastrin
Disorders	(Ncstn); PEN-2
Others	Nos1; Parp1; Nat1; Nat2
Prion-related Disorders	Prp
ALS	SOD1; ALS2; STEX; FUS; TARD BP; VEGF (VEGF-a;
	VEGF-b; VEGF-c)
Drug Addiction	Prkce (alcohol); Drd2; Drd4; ABAT (alcohol); GRIA2;
	Grm5; Grin1; Htr1b; Grin2a; Drd3; Pdyn; Gria1 (alcohol)
Autism	Mecp2; BZRAP1; MDGA2; Sema5A; Neurexin 1; Fragile X (FMR2
	(AFF2); FXR1; FXR2; Mglur5)
Alzheimer's Disease	E1; CHIP; UCH; UBB; Tau; LRP; PICALM; Clusterin; PS1; SORL1;
	CR1; Vld1r; Uba1; Uba3; CHIP28 (Aqp1,
	Aquaporin 1); Uchl1; Uchl3; APP
Inflammation	IL-10; IL-1 (1L-la; IL-lb); IL-13; IL-17 (IL-17a (CTLA8);IL-17b; IL-
	17c; IL-17d; IL-171); 11-23; Cx3crl; ptpn22; TNFa; NOD2/CARD15
	for IBD; IL-6; IL-12 (IL-12a; IL-12b); CTLA4; Cx3cll
Parkinson's Disease	x-Synuclcin; DJ-1; LRRK2; Parkin; PINK1

TABLE 2

CELLULAR FUNCTION	GENES

Blood and coagulation	Anemia (CRAN1, CDA1, RPS19, DBA, PKLR, PK1, NT5C3,
diseases and disorders	UMPH1, PSNI, RHAG, RH50A, NRAMP2, SPTB, ALAS2, ANH1,
	ASB, ABC67, ABC7, ASAT); Bare lymphocyte syndrome
	(TAPBP, TPSN, TAP2, ABCB3, PSF2, RING11, MHC2TA, C2TA,
	RFX5, RFXAP, RFX5), Bleeding disorders (TBXA2R, P2RX1,
	P2X1); Factor Hand factor H-like 1 (HF1, CFH, HUS); Factor V
	and Factor VIII (MCFD2); Factor VII deficiency (F7); Factor X
	deficiency (FIO); Factor XI deficiency (F11); Factor XII
	deficiency (F12, HAF); Factor XIIIA deficiency (F13Al, F13A);
	Factor XIIIB deficiency (F13B); Fanconi anemia (FANCA, FACA,
	FA1, FA, FAA, FAAP95, FAAP90, FLJ34064, FANCB, FANCC,
	FACC, BRCA2, FANCDI, FANCD2, FANCD,
	FACD, FAD, FANCE, FACE, FANCF, XRCC9, FANCG, BR1PI,
	BACH1, FANCJ, PHF9, FANCL, FANCM, KIAA1596);
	Hemophagocytic lymphohistiocytosis disorders (PRF1, HPLH2,
	UNC13D, MUNC13-4, HPLH3, HLH3, FHL3); Hemophilia A (F8,
	FSC, HEMA); Hemophilia B (F9, HEMB), Hemorrhagic
	disorders (PI, ATT, F5); Leukocyte deficiencies and disorders
	(ITGB2, CD18, LCAMB, LAD, EIF261, EIF2BA, I1F2B2, EIF2B3,
	EIF2B5, LVWM, CACH, CLE, EIF2B4); Sickle cell anemia (HBB);
	Thalassemia (HBA2, HBB, HBD, LCRB, HBA1).
Cell dysregulation and	B-cell non-Hodgkin lymphoma (BCL7A, BCL7); Leukemia (TALI,
oncology diseases and	TCL5, SCL, TAL2, FLT3, NBS1, NBS, ZNFN1A1, 1KI, LYF1, HOXD4,
disorders	HOX4B, BCR, CML, PHL, ALL, ARNT, KRAS2, RASK2, GMPS,
	AFIO, ARHGEF12, LARG, KIAA0382, CALM, CLTH, CEBPA, CEBP,
	CHIC2, BTL, FLT3, KIT, PBT, LPP, NPMI, NUP214, D9546E, CAN,
	CAIN, RUNXI, CBFA2, AMLI, WHSC1LI, NSD3, FLT3, AF1Q,
	NPM1, NUMA1, ZNF145, PLZF, PML, MYL, STAT5B, AF1Q,
	CALM, CLTH, ARL11, ARLTS1, P2RX7, P2X7, BCR, CML, PHL,
	ALL, GRAF, NF1, VRNF, WSS, NFNS, PTPNII, PTP2C, SHP2, NS1,
	BCL2, CCND1, PRAD1, BCL1, TCRA, GATA1, GF1, ERYF1, NFE1,
	ABLI, NQO1, DIA4, NMOR1, NUP214, D9546E, CAN, CAIN).
Inflammation and immune	AIDS (KIR3DL1, NKAT3, NKB1, AMB11, K1R3D51, IFNG,
related diseases and	CXCL12, SD F1); Autoimmune lymphoproliferative syndrome
disorders	(TNFRSF6, APT1,
	FAS, CD95, ALPS1A); Combined immunodeficiency, (IL2RG,
	SCIDX1, SCIDX, IMD4); HN-1 (CCL5, SCYA5, D17S136E,
	TCP228), HIV susceptibility or infection (IL10, CSIF, CMKBR2,
	CCR2, CMKBR5, CCCKR5 (CCR5)); Immunodeficienies (CD3E,
	CD3G, AICDA, AID, HIGM2, TNFRSF5, CD40, UNG, DGU,
	HIGM4, TNFSFS, CD40LG, HIGM1, IGM, FOXP3, IPEX, AIID,
	XPID, PIDX, TNFRSF146, TACI; Inflammation (IL-10, IL-1 (IL-la,
	IL-lb), 11-13, IL-17 (IL-17a (CTLA8), IL-17b, IL-17c, IL-17d, IL-
	171), IL-23, Cx3crl, ptpn22, TNFa, NOD2/CARD15 for IBD, IL-
	6, IL-12 (IL-12a, IL-12b), CTLA4, Cx3c11); Severe combined
	immunodeficiencies (SCIDs)(JAK3, JAKL, DCLREIC, ARTEMIS,
	SCIDA, RAG1, RAG2, ADA, PTPRC, CD45, LCA, IL7R, CD3D, T3D,
	IL2RG, SCIDXI, SCIDX, IMD4).
Metabolic, liver, kidney and	Amyloid neuropathy (TTR, PALB); Amyloidosis (APOA1, APP,
protein diseases and	AAA, CVAP, AD1, GSN, FGA, LYZ, TTR, PALB); Cirrhosis (KRT18,
disorders	KRT8, CIRH1A, NAIC, TEX292, KIAA1988); Cystic fibrosis (CFTR,
	ABCC7, CF, MRP7); Glycogen storage diseases (SLC2A2,
	GLUT2, G6PC, G6PT, G6PT1, GAA, LAMP2, LAM PB, AGL, GDE,
	GBE1, GYS2, PYGL, PFKM); Hepatic adenoma, 142330 (TCF1,
	HNF1A, MODY3), Hepatic failure, early onset, and neurologic
	disorder (SCOD1, SCO1), Hepatic lipase deficiency (LIPC),
	Hepatoblastoma, cancer and carcinomas (CTNNB1, PDGFRL,
	PDGRL, PRLTS, AX1NI, AXIN,
	CTNNB1, TP53, P53, LFS1, IGF2R, MPRI, MET, CASP8, MCH5;
	Medullary cystic kidney disease (UMOD, HNFJ, FJHN, MCKD2,
	ADMCKD2); Phenylketonuria (PAH, PKU1, QDPR, DHPR, PTS);
	Polycystic kidney and hepatic disease (FCYT, PKHD1, ARPKD,
	PKD1, PKD2, PKD4, PKDTS, PRKCSH, G19P1, PCLD, 5EC63).
Muscular/skeletal diseases	Becker muscular dystrophy (DMD, BMD, MYF6), Duchenne
and disorders	Muscular Dystrophy (DMD, BMD); Emery-Dreifuss muscular
	dystrophy (LMNA, LMN1, EMD2, FPLD, CMDIA, HGPS,
	LGMDIB, LMNA, LMNI,
	EMD2, FPLD, CMD1A); Facioscapulohumeral muscular
	dystrophy (FSHMD1A, FSHD1A); Muscular dystrophy (FKRP,
	MDC1C, LGMD2I, LAMA2, LAMM, LARGE, KIAA0609, MDC1D,
	FCMD, TTID, MYOT, CAPN3, CANP3, DYSF, LGMD2B, SGCG,
	LGMD2C, DMDA1, SCG3, SGCA, ADL, DAG2, LGMD2D,
	DMDA2, SGCB, LGMD2E, SGCD, SGD, LGMD2F, CMD1L, TCAP,
	LGMD2G, CMD1N, TRIM32, HT2A, LGMD2H, FKRP, MDCIC,
	LCMD21, UN, CMD1G, TMD, LGMD2J, POMT1, CAV3,
	LGMD1C, SEPN1, SELN, RSMD1, PLEC1, PLTN, EBS1);
	Osteopetrosis (LRP5, BMND1, LRP7, LR3, OPPG, VBCH2,
	CLCN7, CLC7, OPTA2, OSTMI, GL, TCIRG1, TIRC7, OC116,
	OPTB1); Muscular atrophy (VAPB, VAPC, ALS8, SMN1, SMA1,
	SMA2, SMA3, SMA4, BSCL2, SPG17, GARS, SMAD1, CMT2D,
	HEXB, IGHMBP2, SMUBP2, CATF1, SMARD1).
Neurological and neuronal	ALS (SOD1, ALS2, STEX, FUS, TARDBP, VEGF (VEGF-a, VEGF-b,
diseases and disorders	VEGF-c); Alzheimer disease (APP, AAA, CVAP, AD1, APOE,
	AD2, PSEN2, AD4, STM2, APBB2, FE65LI, NOS3, PLAU, URK,
	ACE, DCPI, ACEI, MPO, PAC1PI, PAXIPIL, PTIP, A2M, BLMH,
	BMH, PSEN1, AD3); Autism (Mecp2, BZRAP1, MDGA2,
	Sema5A, Neurexin 1, GLO1, MECP2, RTT, PPMX, MRX16,
	MRX79, NLGN3, NLGN4, KIAA1260, AUTSX2); Fragile X
	Syndrome (FMR2, FXR1, FXR2,
	mGLUR5), Huntington's disease and disease like disorders
	(HD, IT15, PRNP, PRIP, JPH3, JP3, HDL2, TBP, SCA17);
	Parkinson disease (NR4A2, NURR1, NOT, TINUR, SNCAIP, TBP,
	SCA17, SNCA,
	NACP, PARK1, PARK4, DJ1, PARK7, LRRK2, PARK8, PINK1,
	PARK6, UCHL1, PARK5, SNCA, NACP, PARK1, PARK4, PRKN,
	PARK2, PDJ, DBH, NDUFV2); Rett syndrome (MECP2, RTT,
	PPMX, MRX16, MRX79, CDKL5, STK9, MECP2, RU, PPMX,
	MRX16, MRX79, x-Synuclein, DJ-1); Schizophrenia
	(Neuregulin1 (Nrg1), Erb4 (receptor for Neuregulin),
	Complexin1 (Cplx1), Tph1 Tryptophan
	hydroxylase, Tph2, Tryptophan hydroxylase 2, Neurexin 1,
	GSK3, GSK3a, GSK3b, 5-HU (Slc6a4), CONT, DRD (Drd1a),
	SLC6A13, DAOA, DTNBP1, Dao (Dao1)); Secretase Related
	Disorders (APH-1 (alpha and beta), Presenilin (Psen1),
	nicastrin, (Ncstn), PEN-2, Nos1, Parp1, Nat1, Nat2);
	Trinucleotide Repeat Disorders (HTT (Huntington's Dx),
	SBMA/SMAX1/AR (Kennedy's Dx), FXN/X25 (Friedrich's
	Ataxia), ATX3 (Machado-Joseph's Dx), ATXN1 and ATXN2
	(spinocerebellar ataxias), DMPK (myotonic dystrophy),
	Atrophin-1 and Atn1 (DRPLA Dx), CBP (Creb-BP-global
	instability), VLDLR (Alzheimer's), Atxn7, Atxn10)
Ocular diseases and	Age-related macular degeneration (Aber, Ccl2, Cc2, cp
disorders	(ceruloplasmin), Timp3, cathepsinD, Vldlr, Ccr2); Cataract
	(CRYAA, CRYA1, CRYBB2, CRYB2, PITX3, BFSP2, CP49, CP47,
	CRYAA, CRYAI, PAX6, AN2 MGDA, CRYBA1, CRYB1, CRYGC,
	CRYG3, CCL, LIM2, MP19, CRYGD, CRYG4, BFSP2, CP49, CP47,
	HSF4, CTM, HSF4, CTM, MIP, AQPO, CRYAB, CRYA2, CTPP2,
	CRYBB1, CRYGD, CRYG4, CRYBB2, CRYB2, CRYGC, CRYG3, CCL,
	CRYAA, CRYA1, GJA8, CX50, CAE1, GJA3, CX46, CZP3, CAE3,
	CCM1, CAM, KRIT1); Corneal clouding and dystrophy (APOA1,
	TGFBI, CSD2, CDGG1, CSD, BIGH3, CDG2, TACSTD2, TROP2,
	M1SI, VSX1, RINX, PPCD, PPD, KTCN, COL8A2, FECD, PPCD2,
	PIP5K3, CFD); Cornea plana congenital (KERA, CNA2);
	Glaucoma (MYOC, TIGR, GLCIA, JOAG,
	GPOA, OPTN, GLC1E, FIP2, HYPL, NRP, CYP161, GLC3A, OPA1,
	NTG, NPG, CYP161, GLC3A); Leber congenital amaurosis
	(CRB1, RP12, CRX, CORD2, CRD, RPGRIPI, LCA6, CORD9,
	RPE65, RP20, AIPL1, LCA4, GUCY2D, GUC2D, LCA1, CORD6,
	RDH12, LCA3); Macular dystrophy (ELOVL4, ADMD, STGD2,
	STGD3, RDS, RP7, PRPH2, PRPH, AVMD, AOFMD, VMD2).
Epilepsy	NHLRC1, EPM2A, EPM2B
Duchenne muscular	DMD, BMD
dystrophy
AIDS	KIR3DL1, NKAT3, NKB1, AMB11, KIR3DS1, IFNG, CDDCL12,
	SDF1
Alpha 1-Antitrypsin	SERPINA1 [serpin peptidase inhibitor, cladeA (alpha-1
Deficiency	antiproteinase, antitrypsin), member 1]; SERPINA2 [serpin
	peptidase inhibitor, cladeA (alpha-1 antiproteinase,
	antitrypsin), member 2]; SERPINA3 [serpin peptidase
	inhibitor, clade A (alpha-1 antiproteinase, antitrypsin),
	member 3]; SERPINA5 [serpin peptidase inhibitor, clade A
	(alpha-1 antiproteinase, antitrypsin), member 5]; SERPINA6
	[serpin peptidase inhibitor, clade A (alpha-1 antiproteinase,
	antitrypsin), member 6];
	SERPINA7 [serpin peptidase inhibitor, Glade A (alpha-1
	antiproteinase, antitrypsin), member 7]; SERPINA6 (serpin
	peptidase inhibitor, cladeA (alpha-1 antiproteinase,
	antitrypsin), member 6)

TABLE 3

CELLULAR FUNCTION	GENES

PI3K/AKT Signaling	PRKCE; ITGAM; ITGA5; IRAK1; PRKAA2; EIF2AK2; PTEN; EIF4E:
	PRKCZ; GRK6: MAPK1; TSC1; PLK1; AKT2; IKBKB; PIK3CA;
	CDK8; CDKN1B; NFKB2; BCL2; PIK3CB; PPP2R1A; MAPK8;
	BCL2LI; MAPK3; TSC2; ITGA1; KRAS; EIF4EBP1; RELA; PRKCD;
	NOS3; PRKAA1; MAPK9; CDK2; PPP2CA; PIM!; ITGB7; YWHAZ;
	ILK; TP53; RAF!; IKBKG; RELB; DYRK1A; CDKNIA; ITGB1;
	MAP2K2; JAK1; AKT1; JAK2; PIK3RI; CHUK; PDPK1; PPP2R5C;
	CTNNB1; MAP2K1; NFKB1; PAK3; ITGB3; CCND1; GSK3A;
	FRAP!; SFN; ITGA2; TTK; CSNK1A1; BRAF; GSK3B; AKT3;
	FOXO1; SGK; HSP90AA1; RPS6KB1
ERK/MAPK Signaling	PRKCE; ITGAM; ITGA5; HSPB1; IRAK1; PRKAA2; EIF2AK2;
	RAC1; RAP1A; TLN1; EIF4E; ELK1; GRK6; MAPK1; RAC2; PLK1;
	AKT2; PIK3CA; CDK8; CREB1; PRKC1; PTK2; FOS; RPS6KA4;
	PIK3CB; PPP2R1A; PIK3C3; MAPK8; MAPK3; ITGA1; ETSI;
	KRAS; MYCN; EIF4EBP1; PPARG; PRKCD; PRKAA1; MAPK9;
	SRC; CDK2; PPP2CA; PIM1; PIK3C2A; ITGB7; YWHAZ; PPP1CC;
	KSR1; PXN; RAF!; FYN; DYRK1A; ITGB1; MAP2K2; PAK4;
	PIK3RI; STAT3; PPP2R5C; MAP2K1; PAK3; ITGB3; ESR1; ITGA2;
	MYC; TTK; CSNK1A1; CRKL; BRAF; ATF4; PRKCA; SRF; STAT1;
	SGK
Glucocorticoid Receptor	RAC1; TAF4B; EP300; SMAD2; TRAF6; PCAF; ELK1; MAPKI;
Signaling	SMAD3; AKT2; IKBKB; NCOR2; UBE21; PIK3CA; CREBI; FOS;
	HSPA5; NFKB2; BCL2; MAP3K14; STAT5B; PIK3CB; PIK3C3;
	MAPK8; BCL2L1; MAPK3; T5C22D3; MAPK10; NRIP1; KRAS;
	MAPK13; RELA; STAT5A; MAPK9; NOS2A; PBX1; NR3C1;
	PIK3C2A; CDKN1C; TRAF2; SERPINE1; NCOA3; MAPK14; TNF;
	RAF1; IKBKG; MAP3K7; CREBBP; CDKN1A; MAP2K2; JAK1; IL8;
	NCOA2; AKT1; JAK2; PIK3R1; CHUK; STAT3; MAP2K1; NFKB1;
	TGFBR1; ESR1; SMAD4; CEBPB; WN; AR; AKT3; CCL2; MMP1;
	STAT1; IL6; HSP90AA1
Axonal Guidance Signaling	PRKCE; ITGAM; ROCK1; ITGA5; CXCR4; ADAM12; IGF1; RAC1;
	RAP1A; EIF4E; PRKCZ; NRP1; NTRK2; ARHGEF7; SMO; ROCK2;
	MAPK1; PGF; RAC2; PTPN11; GNAS; AKT2; PIK3CA; ERBB2;
	PRKCI; PTK2; CFL1; GNAQ; PIK3CB; CXCL12; PIK3C3; WNT11;
	PRKD1; GNB2L1; ABL1; MAPK3; ITGA1; KRAS; RHOA; PRKCD;
	PIK3C2A; ITGB7; GLI2; PXN; VASP; RAF1; FYN; ITGB1;
	MAP2K2; PAK4; ADAM17; AKT1; PIK3R1; GLI1; WNT5A;
	ADAM10; MAP2K1; PAK3; ITGB3; CDC42; VEGFA; ITGA2;
	EPHA8; CRKL; RND1; GSK3B; AKT3; PRKCA
Ephrin Receptor Signaling	PRKCE; ITGAM; ROCK1; ITGA5; CXCR4; IRAK1; PRKAA2;
	EIF2AK2; RAC1; RAP1A; GRK6; ROCK2; MAPK1; PGF; RAC2;
	PTPN11; GNAS; PLK1; AKT2; DOK1; CDK8; CREB1; PTK2; CFL1;
	GNAQ; MAP3K14; CXCL12; MAPK8; GNB2L1; ABL1; MAPK3;
	ITGA1; KRAS; RHOA; PRKCD; PRKAA1; MAPK9; SRC; CDK2;
	PIM1; ITGB7; PXN; RAF1; FYN; DYRK1A; ITGB1; MAP2K2;
	PAK4, AKT1; JAK2; STAT3;ADAM10; MAP2K1; PAK3; ITGB3;
	CDC42; VEGFA; ITGA2; EPHA8; UK; CSNK1A1; CRKL; BRAF;
	PTPN13; ATF4; AKT3; SGK
Actin Cytoskeleton Signaling	ACTN4; PRKCE; ITGAM; ROCK1; ITGA5; IRAK1; PRKAA2;
	EIF2AK2; RAC1; INS; ARHGEF7; GRK6; ROCK2; MAPK1; RAC2;
	PLK1; AKT2; PIK3CA; CDK8; PTK2; CPL1; PIK3CB; MYH9;
	DIAPH1; PIK3C3; MAPK8; F2R; MAPK3; SLC9A1; ITGA1; KRAS;
	RHOA; PRKCD; PRKAA1; MAPK9; CDK2; PIM1, PIK3C2A; ITGB7;
	PPP1CC; PXN; VIL2; RAF1; GSN; DYRK1A; ITGB1; MAP2K2;
	PAK4; PIP5K1A; PIK3R1; MAP2K1; PAK3; ITGB3; CDC42; APC;
	ITGA2; TTK; CSNK1A1; CRKL; BRAF; VAV3; SGK
Huntington's Disease	PRKCE; IGF1; EP300; RCOR1; PRKCZ; HDAC4; TGM2; MAPK1;
Signaling	CAPNS1; AKT2; EGFR; NCOR2; SP1; CAPN2; PIK3CA; HDAC5;
	CREB1; PRKCI; HSPA5; REST; GNAQ; PIK3CB; PIK3C3; MAPK8;
	IGF1R; PRKD1; GNB2L1; BCL2L1; CAPN1; MAPK3; CASP8;
	HDAC2; HDAC7A; PRKCD; HDAC11; MAPK9; HDAC9; PIK3C2A;
	HDAC3; TP53; CASP9; CREBBP; AKT1; PIK3R1; PDPK1; CASP1;
	APAF1; FRAP1; CASP2; JUN; BAX; ATF4; AKT3; PRKCA; CLTC;
	SGK; HDAC6; CASP3
Apoptosis Signaling	PRKCE; ROCK1; BID; IRAK1; PRKAA2; EIF2AK2; BAK1; BIRC4;
	GRK6; MAPK1; CAPNS1; PLK1; AKT2; IKBKB; CAPN2; CDK8;
	FAS; NFKB2; BCL2; MAP3K14; MAPK8; BCL2L1; CAPN1;
	MAPK3; CASP8; KRAS; RELA; PRKCD; PRKAA1; MAPK9; CDK2;
	PIM1; TP53; TNF; RAF1; IKBKG; RELB; CASP9; DYRK1A;
	MAP2K2; CHUK; APAF1; MAP2K1; NFKB1; PAK3; LMNA;
	CASP2; BIRC2; TTK; CSNKIA1; BRAF; BAX; PRKCA; SGK; CASP3;
	BIRC3; PARP1
B Cell Receptor Signaling	RAC1; PTEN; LYN; ELK1; MAPK1; RAC2; PTPN11; AKT2; IKBKB;
	PIK3CA; CREB1; SYK; NFKB2; CAMK2A; MAP3K14; PIK3CB;
	PIK3C3; MAPK8; BCL2L1; ABL1; MAPK3; ETS1; KRAS; MAPK13;
	RELA; PTPN6; MAPK9; EGRI; PIK3C2A; BTK; MAPK14; RAFI;
	IKBKG; RELB; MAP3K7; MAP2K2; AKT1; PIK3R1; CHUK;
	MAP2K1; NFKBI; CDC42; GSK3A; FRAPI; BCL6; BCL10; JUN;
	GSK3B; ATF4; AKT3; VAV3; RPS6KB1
Leukocyte Extravasation	ACTN4; CD44; PRKCE; ITGAM; ROCKI; CXCR4; CYBA;
Signaling	RAC1; RANA; PRKCZ; ROCK2; RAC2; PTPNII;
	MMPI4; PIK3CA; PRKCI; PTK2; PIK3CB; CXCL12;
	PIK3C3; MAPK8; PRKD1; ABL1; MAPK10; CYBB;
	MAPK13; RHOA; PRKCD; MAPK9; SRC; PIK3C2A; BTK;
	MAPK14; NOX1; PXN; VIL2; VASP; ITGB1; MAP2K2;
	CTNND1; PIK3R1; CTNNBI; CLDN1; CDC42; F11R; ITK;
	CRKL; VAV3; CTTN; PRKCA; MMP1; MMP9
Integrin Signaling	ACTN4; ITGAM; ROCK1; ITGA5; RAC1; PTEN; RAP1A; TLN1;
	ARHGEF7; MAPK1; RAC2; CAPNS1; AKT2; CAPN2; PIK3CA;
	PTK2; PIK3CB; PIK3C3; MAPK8; CAV1; CAPN1; ABL1; MAPK3;
	ITGA1; KRAS; RHOA; SRC; PIK3C2A; ITGB7; PPPICC; ILK; PXN;
	VASP; RAF1; FYN; ITGB1; MAP2K2; PAK4; AKT1; PIK3R1; TNK2;
	MAP2K1; PAK3; ITGB3; CDC42; RND3; ITGA2; CRKL; BRAF;
	GSK3B; AKT3
Acute Phase Response	IRAK1; SOD2; MYD88; TRAF6; ELK1; MAPK1; PTPN11; AKT2;
Signaling	IKBKB; PIK3CA; FOS; NFKB2; MAP3K14; PIK3CB; MAPK8;
	RIPK1; MAPK3; IL6ST; KRAS; MAPK13; IL6R; RELA; SOCS1;
	MAPK9; FTL; NR3C1; TRAF2; SERPINE1; MAPK14; TNF; RAF1;
	PDK1; IKBKG; RELB; MAP3K7; MAP2K2; AKT1; JAK2; PIK3R1;
	CHUK; STAT3; MAP2K1; NFKB1; FRAP1; CEBPB; JUN; AKT3;
	IL1R1; IL6
PTEN Signaling	ITGAM; ITGA5; RACI1 PTEN; PRKCZ; BCL2L11; MAPKI; RAC2;
	AKT2; EGFR; IKBKB; CBL; PIK3CA; CDKN1B; PTK2; NFKB2;
	BCL2; PIK3CB; BCL2L1; MAPK3; ITGA1; KRAS; ITGB7; ILK;
	PDGFRB; INSR; RAF1; IKBKG; CASP9; CDKN1A; ITGB1;
	MAP2K2; AKT1; PIK3R1; CHUK; PDGFRA; PDPK1; MAP2K1;
	NFKB1; ITGB3; CDC42; CCND1; GSK3A; ITGA2; GSK3B; AKT3;
	FOXO1; CASP3; RPS6KB1
p53 Signaling	PTEN; EP300; BBC3; PCAF; FASN; BRCA1; GADD45A; BIRC5;
	AKT2; PIK3CA; CHEK1; TP53INP1; BCL2; PIK3CB; PIK3C3;
	MAPK8; THBS1; ATR; BCL2L1; E2F1; PMAIP1; CHEK2;
	TNFRSF10B; TP73; RB1; HDAC9; CDK2; PIK3C2A; MAPK14;
	TP53; LRDD; CDKNIA; HIPK2; AKT1; PIK3R1; RRM2B; APAF1;
	CTNNBI; SIRTI; CCNDI; PRKDC; ATM; SFN; CDKN2A; JUN;
	SNAI2; GSK3B; BAX; AKT3
Aryl Hydrocarbon Receptor	HSPR1; EP300; FASN; TGM2; RXRA; MAPK1; NQO1; NCOR2;
Signaling	SP1; ARNT; CDKN1B; FOS; CHEK1; SMARCA4; NEKB2; MAPK8;
	ALDHIA1; ATR; E2F1; MAPK3; NRIP1; CHEK2; RELA; TP73;
	GSTP1; RB1; SRC; CDK2; AHR; NFE2L2; NCOA3; TP53; TNF;
	CDKN1A; NCOA2; APAF1; NFKB1; CCND1; ATM; ESR1;
	CDKN2A; MYC; JUN; ESR2; BAX; IL6; CYP1B1; HSP90AA1
Xenobiotic Metabolism	PRKCE; EP300; PRKCZ; RXRA; MAPK1; NQO1; NCOR2; PIK3CA;
Signaling	ARNT; PRKCI; NFKB2; CAMK2A; PIK3CB; PPP2R1A; PIK3C3;
	MAPK8; PRKD1; ALDH1A1; MAPK3; NRIP1; KRAS; MAPK13;
	PRKCD; GSTP1; MAPK9; NOS2A; ABCB1; AHR; PPP2CA; FTL;
	NFE2L2; PIK3C2A; PPARGC1A; MAPK14; TNF; RAF1; CREBBP;
	MAP2K2; PIK3R1; PPP2R5C; MAP2K1; NFKB1; KEAP1; PRKCA;
	EIF2AK3; IL6; CYP1B1; HSP90AA1
SAPK/JNK Signaling	PRKCE; IRAK1; PRKAA2; EIF2AK2; RAC1; ELK1; GRK6; MAPK1;
	GADD45A; RAC2; PLK1; AKT2; PIK3CA; FADD; CDK8; PIK3CB;
	PIK3C3; MAPK8; RIPK1; GNB2L1; IRS1; MAPK3; MAPK10;
	DAXX; KRAS; PRKCD; PRKAA1; MAPK9; CDK2; PIM1; PIK3C2A;
	TRAF2; TP53; LCK; MAP3K7; DYRK1A; MAP2K2; PIK3R1;
	MAP2K1; PAK3; CDC42; JUN; TTK; CSNK1A1; CRKL; BRAF; SGK
PPAr/RXR Signaling	PRKAA2; EP300; INS; SMAD2; TRAF6; PPARA; FASN; RXRA;
	MAPK1; SMAD3; GNAS; IKBKB; NCOR2; ABCA1; GNAQ;
	NFKB2; MAP3K14; STAT5B; MAPK8; IRS1; MAPK3; KRAS;
	RELA; PRKAA1; PPARGC1A; NCOA3; MAPK14; INSR; RAF1;
	IKBKG; RELB; MAP3K7; CREBBP; MAP2K2; JAK2; CHUK;
	MAP2K1; NFKB1; TGFBR1; SMAD4; JUN; IL1R1; PRKCA; IL6;
	HSP90AA1; ADIPOQ
NF-KB Signaling	IRAK1; EIF2AK2; EP300; INS; MYD88; PRKCZ; TRAF6; TBK1;
	AKT2; EGFR; IKBKB; PIK3CA; BTRC; NFKB2; MAP3K14; PIK3CB;
	PIK3C3; MAPK8; RIPK1; HDAC2; KRAS; RELA; PIK3C2A; TRAF2;
	TLR4; PDGFRB; TNF; INSR; LCK; IKBKG; RELB; MAP3K7;
	CREBBP; AKT1; PIK3R1; CHUK; PDGFRA; NFKB1; TLR2; BCL10;
	GSK3B; AKT3; TNFAIP3; IL1R1
Neuregulin Signaling	ERBB4; PRKCE; ITGAM; ITGA5; PTEN; PRKCZ; ELK1; MAPK1;
	PTPN11; AKT2; EGFR; ERBB2; PRKCI; CDKN1B; STAT5B;
	PRKD1; MAPK3; ITGA1; KRAS; PRKCD; STAT5A; SRC; ITGB7;
	RAF1; ITGB1; MAP2K2; ADAM! 7; AKT1; PIK3RI; PDPK1;
	MAP2K1; ITGB3; EREG; FRAP1; PSEN1; ITGA2; MYC; NRG1;
	CRKL; AKT3; PRKCA; HSP90AA1; RPS6KB1
Wnt & Beta catenin	CD44; EP300; LRP6; DVL3; CSNK1E; GJA1; SMO; AKT2; PIN1;
Signaling	CDH1; BTRC; GNAQ; MARK2; PPP2R1A; WNT11; SRC; DKK1;
	PPP2CA; SOX6; SFRP2; ILK; LEF1; SOX9; TP53; MAP3K7;
	CREBBP; TCF7L2; AKT1; PPP2R5C; WNT5A; LRP5; CTNNB1;
	TGFBR1; CCND1; GSK3A; DVL1; APC; CDKN2A; MYC; CSNK1A1;
	GSK3B; AKT3; SOX2
Insulin Receptor Signaling	PTEN; INS; EIF4E; PTPN1; PRKCZ; MAPK1; TSC1; PTPN11;
	AKT2; CBL; PIK3CA; PRKCI; PIK3CB; PIK3C3; MAPKS; IRS1;
	MAPK3; TSC2; KRAS; EIF4EBP1; SLC2A4; PIK3C2A; PPP1CC;
	INSR; RAF1; FYN; MAP2K2; JAK1; AKT1; JAK2; PIK3RI; PDPK1;
	MAP2K1; GSK3A; FRAP1; CRKL; GSK3B; AKT3; FOXO1; SGK;
	RPS6KB1
IL-6 Signaling	HSPB1; TRAF6; MAPKAPK2; :ELK1; MAPK1; PTPN11; IKBKB;
	FOS; NFKB2; MAP3K14; MAPKS; MAPK3; MAPK10; IL65T;
	KRAS; MAPK13; IL6R; RELA; SOCS1; MAPK9; ABCB1; TRAF2;
	MAPK14; TNF; RAF1; IKBKG; RELB; MAP3K7; MAP2K2, IL8;
	JAK2; CHUK; STAT3; MAP2KI; NFKB1; CEBPB; JUN; IL1R1; SRF;
	IL6
Hepatic Cholestasis	PRKCE; IRAK1; INS; MYDSS; PRKCZ; TRAF6; PPARA; RXRA;
	IKBKB; PRKCI; NFKB2; MAP3K14; MAPKS; PRKD1; MAPK10;
	RELA; PRKCD; MAPK9; ABCB1; TRAF2; TLR4; TNF; INSR; IKBKG;
	RELB; MAP3K7; IL8; CHUK; NR1H2; TJP2; NFKB1; ESR1; REBF1;
	FGFR4; JUN; IL1R1.; PRKCA; IL6
IGF-1 Signaling	IGF1; PRKCZ; ELK1; MAPK1; PTPN11; NEDD4; AKT2; PIK3CA;
	PRKCI; PTK2; FOS; PIK3CB; PIK3C3; MAPKS; IGF1R; IRS1;
	MAPK3; IGFBP7; KRAS; PIK3C2A; YWHAZ; PXN; RAF1; CASP9;
	MAP2K2; AKT1; PIK3R1; PDPK1; MAP2K1; IGFBP2; SFN; JUN;
	CYR61; AKT3; FOXO1; SRF; CTGF; RPS6KB1
NRF2-mediated Oxidative	PRKCE; EP300; SOD2; PRKCZ; MAPK1; SQSTM1; N001;
Stress Response	PIK3CA; PRKCI; FOS; PIK3CB; PIK3C3; MAPK8; PRKD1; MAPK3;
	KRAS; PRKCD; GSTP1; MAPK9; FTL; NFE2L2; PIK3C2A;
	MAPK14; RAF1; MAP3K7; CREBBP; MAP2K2;AKT1; PIK3R1;
	MAP2K1; PPIB; JUN; KEAP1; GSK3B; ATF4; PRKCA; EIF2AK3;
	HSP90AA1
Hepatic Fibrosis/Hepatic	EDN1; IGF1; KDR; FLT1; SMAD2; FGFR1; MET; PGF; SMAD3;
Stellate Cell Activation	EGFR; FAS; CSF1; NFKB2; BCL2; MYH9; IGF1R; IL6R; RELA;
	TLR4; PDGFRB; TNF; RELB; IL8; PDGFRA; NFKB1; TGFBR1;
	SMAD4; VEGFA; BAX; IL1R1; CCL2; HGF; MMP1; STAT1; IL6;
	CTGF; MMP9
PPAR Signaling	EP300; INS; TRAF6; PPARA; RXRA; MAPK1; IKBKB; NCOR2;
	FOS; NFKB2; MAP3K14; STAT5B; MAPK3; NRIP1; KRAS;
	PPARG; RELA; STAT5A; TRAF2; PPARGC1A; PDGFRB; TNF;
	INSR; RAF1; IKBKG; RELB; MAP3K7; CREBBP; MAP2K2; CHUK;
	PDGFRA; MAP2K1; NFKB1; JUN; IL1R1; HSP90AA1
Fc Epsilon R1 Signaling	PRKCE; RAC1; PRKCZ; LYN; MAPK1; RAC2; PTPN11; AKT2;
	PIK3CA; SYK; PRKCI; PIK3CB; PIK3C3; MAPK8; PRKD1; MAPK3;
	MAPK10; KRAS; MAPK13; PRKCD; MAPK9; PIK3C2A; BTK;
	MAPK14; TNF; RAF1; FYN; MAP2K2; AKT1; PIK3RI; PDPK1;
	MAP2K1; AKT3; VAV3; PRKCA
G-Protein Coupled Receptor	PRKCE; RAP1A; RG516; MAPK1; GNAS; AKT2; IKBKB; PIK3CA;
Signaling	CREB1; GNAQ; NFKB2; CAMK2A; PIK3CB; PIK3C3; MAPK3;
	KRAS; RELA; SRC; PIK3C2A; RAF1; IKBKG; RELB; FYN; MAP2K2;
	AKT1; PIK3R1; CHUK; PDPK1; STAT3; MAP2K1; NFKB1; BRAF;
	ATF4; AKT3; PRKCA
Inositol Phosphate	PRKCE; IRAK1; PRKAA2; EIF2AK2; PTEN; GRK6; MAPK1; PLK1;
Metabolism	AKT2; PIK3CA; CDK8; PIK3CB; PIK3C3; MAPK8; MAPK3;
	PRKCD; PRKAA1; MAPK9; CDK2; PIM1; PIK3C2A; DYRK1A;
	MAP2K2; PIP5K1A; PIK3R1; MAP2K1; PAK3; ATM; TTK;
	CSNK1A1; BRAF; SGK
PDGF Signaling	EIF2AK2; ELK1; ABL2; MAPK1; PIK3CA; FOS; PIK3CB; PIK3C3;
	MAPK8; CAV1; ABL1; MAPK3; KRAS; SRC; PIK3C2A; PDGFRB;
	RAF1; MAP2K2; JAK1; JAK2; PIK3R1; PDGFRA; STAT3; SPHK1;
	MAP2KI; MYC; JUN; CRKL; PRKCA; SRF; STAT1; SPHK2
VEGF Signaling	ACTN4; ROCKI; KDR; FLTI; ROCK2; MAPKI; PGF; AKT2;
	PIK3CA; ARNT; PTK2; BCL2; PIK3CB; PIK3C3; BCL2L1; MAPK3;
	KRAS; HIF1A; NOS3; PIK3C2A; PXN; RAFI; MAP2K2; ELAVLI;
	AKTI; PIK3R1; MAP2KI; SFN; VEGFA; AKT3; FOXO1; PRKCA
Natural Killer Cell Signaling	PRKCE; RAC1; PRKCZ; MAPK1; RAC2; PTPN11; KIR2DL3; AKT2;
	PIK3CA; SYK; PRKCI; PIK3CB; PIK3C3; PRKD1; MAPK3; KRAS;
	PRKCD; PTPN6; PIK3C2A; LCK; RAF1; FYN; MAP2K2; PAK4;
	AKT1; PIK3R1; MAP2K1; PAK3; AKT3; VAV3; PRKCA
Cell Cycle: G1/S Checkpoint	HDAC4; SMAD3; SUV39H1; HDAC5; CDKN1B; BTRC; ATR;
Regulation	ABL1; E2F1; HDAC2; HDAC7A; RB1; HDAC11; HDAC9; CDK2;
	E2F2; HDAC3; TP53; CDKN1A; CCND1; E2F4; ATM; RBL2;
	SMAD4; CDKN2A; MYC; NRG1; GSK3B; RBL1; HDAC6
T Cell Receptor Signaling	RAC1; ELK1; MAPK1; IKBKB; CBL; PIK3CA; FOS; NFKB2;
	PIK3CB; PIK3C3; MAPK8; MAPK3; KRAS; RELA; PIK3C2A; BTK;
	LCK; RAF1; IKBKG, RELB; FYN; MAP2K2; PIK3R1; CHUK;
	MAP2K1; NFKBI; ITK; BCL10; JUN; VAV3
Death Receptor Signaling	CRADD; HSPB1; BID; BIRC4; TBK1; IKBKB; FADD; FAS; NFKB2;
	BCL2; MAP3K14; MAPK8; RIPK1; CASP8; DAXX; TNFRSF10B;
	RELA; TRAF2; TNF; IKBKG; RELB; CASP9; CHUK; APAF1; NFKB1;
	CASP2; BIRC2; CASP3; BIRC3
FGF Signaling	RAC1; FGFR1; MET; MAPKAPK2; MAPK1; PTPN11; AKT2;
	PIK3CA; CREB1; PIK3CB; PIK3C3; MAPK8; MAPK3; MAPK13;
	PTPN6; PIK3C2A; MAPK14; RAF1; AKT1; PIK3R1; STAT3;
	MAP2K1; FGFR4; CRKL; ATF4; AKT3; PRKCA; HGF
GN-CSF Signaling	LYN; ELK1; MAPK1; PTPN11; AKT2; PIK3CA; CAMK2A; STAT5B;
	PIK3CB; PIK3C3; GNB2L1; BCL2L1; MAPK3; ETS1; KRAS;
	RUNX1; PIM1; PIK3C2A; RAF1; MAP2K2; AKT1; JAK2; PIK3R1;
	STAT3; MAP2K1; CCND1; AKT3; STAT1
Amyotrophic Lateral	BID; IGF1; RAC1; BIRC4; PGF; CAPNS1; CAPN2; PIK3CA; BCL2;
Sclerosis Signaling	PIK3CB; PIK3C3; BCL2L1; CAPN1; PIK3C2A; TP53; CASP9;
	PIK3R1; RAB5A; CASP1; APAF1; VEGFA; BIRC2; BAX; AKT3;
	CASP3; BIRC3
JAK/Stat Signaling	PTPN1; MAPK1; PTPN11; AKT2; PIK3CA; STAT5B; PIK3CB;
	PIK3C3; MAPK3; KRAS; SOCS1; STAT5A; PTPN6; PIK3C2A;
	RAFI; CDKN1A; MAP2K2; JAK1; AKT1; JAK2; PIK3R1; STAT3;
	MAP2KI; FRAP1; AKT3; STAT1
Nicotinate and Nicotinamide	PRKCE; IRAK1; PRKAA2; EIF2AK2; GRK6; MAPK1; LK1; AKT2;
Metabolism	T2; CDK8; MAPK8; MAPK3; PRKCD; PRKAA1; PBEF1; MAPK9;
	CDK2; PIMI; DYRK1A; MAP2K2; MAP2K1; PAK3; NT5E; TTK;
	CSNK1A1; BRAF; SGK
Chemokine Signaling	CXCR4; ROCK2; MAPK1; PTK2; FOS; CFL1; GNAQ; CAMK2A;
	CXCL12; MAPK8; MAPK3; KRAS; MAPK13; RHOA; CCR3; SRC;
	PPP1CC; MAPK14; NOX1; RAF1; MAP2K2; MAP2K1; JUN;
	CCL2; PRKCA
IL-2 Signaling	ELK1; MAPK1; PTPN11; AKT2; PIK3CA; SYK; FOS; STAT5B;
	PIK3CB; PIK3C3; MAPK8; MAPK3; KRAS; SOCS1; STAT5A;
	PIK3C2A; LCK; RAF1; MAP2K2; JAK1; AKT1; PIK3R1; MAP2K1;
	JUN; AKT3
Synaptic Long Term	PRKCE; IGF1; PRKCZ; PRDX6; LYN; MAPK1; GNAS; PRKCI;
Depression	GNAQ; PPP2R1A; IGF1R; PRKD1; MAPK3; KRAS; GRN; PRKCD;
	NOS3; NOS2A; PPP2CA; YWHAZ; RAF1; MAP2K2; PPP2R5C;
	MAP2K1; PRKCA
Estrogen Receptor Signaling	TAF4B; EP300; CARM1; PCAF; MAPK1; NCOR2; SMARCA4;
	MAPK3; NRIP1; KRAS; SRC; NR3C1; HDAC3; PPARGG1A;
	RBM9; NCOA3; RAF1; CREBBP; MAP2K2; NCOA2; MAP2K1;
	PRKDC; ESR1; ESR2
Protein Ubiquitination	TRAF6; SMURF1; BIRC4; BRCA1; UCHL1; NEDD4; CBL; UBE2I;
Pathway	BTRC; HSPA5; USP7; USP10; FBXW7; USP9X; STUB1; USP22;
	B2M; BIRC2; PARK2; USP8; USP1; VHL; HSP90AA1; BIRC3
IL-10 Signaling	TRAF6; CCR1; ELK1; IKBKB; SP1; FOS; NFKB2; MAP3K14;
	MAPK8; MAPK13; RELA; MAPK14; TNF; IKBKG; RELB;
	MAP3K7; JAK1; CHUK; STAT3; NFKB1; JUN; IL1R1.; IL6
VDR/RXR Activation	PRKCE; EP300; PRKCZ; RXRA; GADD45A; HES1; NCOR2; SP1;
	PRKCI; CDKN1B; PRKD1; PRKCD; RUNX2; KLF4; YY1; NCOA3;
	CDKN1A; NCOA2; SPP1; LRP5; CEBPB; FOXO1; PRKCA
TGF-beta Signaling	EP300; SMAD2; SMURF1; MAPK1; SMAD3; SMAD1; FOS;
	MAPK8; MAPK3; KRAS; MAPK9; RUNX2; SERPINE1; RAF1;
	MAP3K7; CREBBP; MAP2K2; MAP2K1; TGFBR1; SMAD4; JUN;
	SMAD5
Toll-like Receptor Signaling	IRAK1; EIF2AK2; MYD88; TRAF6; PPARA; ELK1; IKBKB; FOS;
	NFKB2; MAP3K14; MAPK8; MAPK13; RELA; TLR4; MAPK14;
	IKBKG; RELB; MAP3K7; CHUK; NFKB1; TLR2; JUN
P38 MAPK Signaling	HSPB1; IRAK1; TRAF6; MAPKAPK2; ELK1; FADD; FAS; CREB1;
	DDIT3; RPS6KA4; DAXX; MAPK13; TRAF2; MAPK14; TNF;
	MAP3K7; TGFBR1; MYC; ATF4; IL1R1; SRF; STAT1
Neurotrophin/TRK Signaling	NTRK2; MAPK1; PTPN11; PIK3CA; CREB1; FOS; PIK3CB;
	PIK3C3; MAPK8; MAPK3; KRAS; PIK3C2A; RAF1; MAP2K2;
	AKT1; PIK3R1; PDPK1; MAP2K1; CDC42; JUN; ATF4
FXR/RXR Activation	INS; PPARA; FASN; RXRA; AKT2; SDC1; MAPK8; APOB;
	MAPK10; PPARG; MTTP; MAPK9; PPARGC1A; TNF; CREBBP;
	AKT1; SREBF1; FGFR4; AKT3; FOXO1
Synaptic Long Term	PRKCE; RAP1A; EP300; PRKCZ; MAPK1; CREB1; PRKCI; GNAQ;
Potentiation	CAMK2A; PRKD1; MAPK3; KRAS; PRKCD; PPP1CC; RAF1;
	CREBBP; MAP2K2; MAP2K1; ATF4; PRKCA
Calcium Signaling	RAP1A; EP300; HDAC4; MAPK1; HDAC5; CREB1; CAMK2A;
	MYH9; MAPK3; HDAC2; HDAC7A; HDAC11; HDAC9; HDAC3;
	CREBBP; CALR; CAMKK2; ATF4; HDAC6
EGF Signaling	ELK1; MAPK1; EGFR; PIK3CA; FOS; PIK3CB; PIK3C3; MAPK8;
	MAPK3; PIK3C2A; RAF1; JAK1; PIK3R1; STAT3; MAP2K1; JUN;
	PRKCA; SRF; STAT1
Hypoxia Signaling in the	EDN1; PTEN; EP300; NQO1; UBE2I; CREB1; ARNT; HIF1A;
Cardiovascular System	SLC2A4; NOS3; TP53; LDHA; AKT1; ATM; VEGFA; JUN; ATF4;
	VHL; HSP90AA1
LPS/IL-1 Mediated Inhibition	IRAK1; MYD88; TRAF6; PPARA; RXRA; ABCA1; MAPK8;
of RXR Function	ALDH1A1; GSTP1; MAPK9; ABCB1; TRAF2; TLR4; TNF;
	MAP3K7; NR1H2; SREBF1; JUN; IL1R1
LXR/RXR Activation	FASN; RXRA; NCOR2; ABCA1; NFKB2; IRF3; RELA; NOS2A;
	TLR4; TNF; RELB; LDLR; NR1H2; NFKB1; SREBF1; IL1R1.; CCL2;
	IL6; MMP9
Amyloid Processing	PRKCE; CSNK1E; MAPK1; CAPNS1; AKT2; CAPN2; CAPN1;
	MAPK3; MAPK13; MAPT; MAPK14; AKT1; PSEN1; CSNK1A1;
	GSK3B; AKT3; APP
IL-4 Signaling	AKT2; PIK3CA; PIK3CB; PIK3C3; IRS1; KRAS; SOCS1; PTPN6;
	NR3C1; PIK3C2A; JAK1; AKT1; JAK2; PIK3R1; FRAP1; AKT3;
	RPS6KB1
Cell Cycle: G2/M DNA	EP300; PCAF; BRCA1; GADD45A; PLK1; BTRC; CHEK1; ATR;
Damage Checkpoint	CHEK2; YWHAZ; TP53; CDKN1A; PRKDC; ATM; SFN; CDKN2A
Regulation
Nitric Oxide Signaling in the	KDR; FLT1; PGF; AKT2; PIK3CA; PIK3CB; PIK3C3; CAV1; PRKCD;
Cardiovascular System	N053; PIK3C2A; AKT1; PIK3R1; VEGFA; AKT3; HSP90AA1
Purine Metabolism	NME2; SMARCA4; MYH9; RRM2; ADAR; EIF2AK4; PKM2;
	ENTPD1; RAD51; RRM2B; TJP2; RAD51C; NT5E; POLD1; NME1
cAMP-mediated Signaling	RAP1A; MAPK1; GNAS; CREB1; CAMK2A; MAPK3; SRC; RAF1;
	MAP2K2; STAT3; MAP2K1; BRAF; ATF4
Mitochondrial Dysfunction	SOD2; MAPK8; CASP8; MAPK10; MAPK9; CASP9; PARK7;
	PSEN1; PARK2; APP; CASP3
Notch Signaling	HES1; JAG1; NUMB; NOTCH4; ADAM17; NOTCH2; PSEN1;
	NOTCH3; NOTCH1; DLL4
Endoplasmic Reticulum	HSPA5; MAPK8; XBP1; TRAF2; ATF6; CASP9; ATF4; EIF2AK3;
Stress Pathway	CASP3
Pyrimidine Metabolism	NME2; AICDA; RRM2; EIF2AK4; ENTPD1; RRM2B; NT5E;
	POLD1; NME1
Parkinson's Signaling	UCHL1; MAPK8; MAPK13; MAPK14; CASP9; PARK7; PARK2;
	CASP3
Cardiac & Beta Adrenergic	GNAS; GNAQ; PPP2R1A; GNB2L1; PPP2CA; PPP1CC; PPP2R5C
Signaling
Glycolysis/Gluconeogenesis	HK2; GCK; GPI; ALDH1A1; PKM2; LDHA; HK1
Interferon Signaling	IRF1; SOCS1; JAK1; JAK2; IFITM1; STAT1; IFIT3
Sonic Hedgehog Signaling	ARRB2; SMO; GLI2; DYRK1A; GLI1; G5K39; DYRK1B
Glycerophospholipid	PLD1; GRN; GPAM; YWHAZ; SPHK1; SPHK2
Metabolism
Phospholipid Degradation	PRDX6; PLD1; GRN; YWHAZ; SPHK1; SPHK2
Tryptophan Metabolism	SIAH2; PRMT5; NEDD4; ALDH1A1; CYP161; SIAH1
Lysine Degradation	SUV39H1; EHMT2; NSD1; SETD7; PPP2R5C
Nucleotide Excision Repair	ERCC5; ERCC4; XPA; XPC; ERCC1
Pathway
Starch and Sucrose	UCHL1; HK2; GCK; GPI; HK1
Metabolism
Aminosugars Metabolism	NQO1; HK2; GCK; HK1
Arachidonic Acid	PRDX6; GRN; YWHAZ; CYP1B1
Metabolism
Circadian Rhythm Signaling	CSNK1E; CREB1; ATF4; NR1D1
Coagulation System	BDKRB1; F2R; SERPINE1; F3
Dopamine Receptor	PPP2R1A; PPP2CA; PPP1CC; PPP2R5C
Signaling
Glutathione Metabolism	IDH2; GSTP1; ANPEP; IDH1
Glycerolipid Metabolism	ALDH1A1; GPAM; SPHK1; SPHK2
Linoleic Acid Metabolism	PRDX6; GRN; YWHAZ; CYP1B1
Methionine Metabolism	DNMT1; DNMT3B; AHCY; DNMT3A
Pyruvate Metabolism	GLO1; ALDH1A1; PKM2; LDHA
Arginine and Proline	ALDH1A1; NOS3; NOS2A
Metabolism
Eicosanoid Signaling	PRDX6; GRN; YWHAZ
Fructose and Mannose	HK2; GCK; HK1
Metabolism
Galactose Metabolism	HK2; GCK; HK1
Stilbene, Coumarine and	PRDX6; PRDX1; TYR
Lignin Biosynthesis
Antigen Presentation	CALR; B2M
Pathway
Biosynthesis of Steroids	NQO1; DHCR7
Butanoate Metabolism	ALDH1A1; NLGN1
Citrate Cycle	IDH2; IDH1
Fatty Acid Metabolism	ALDH1A1; CYP1B1
Glycerophospholipid	PRDX6; CHKA
Metabolism
Histidine Metabolism	PRMT5; ALDH1A1
Inositol Metabolism	ERO1L; APEX1
Metabolism of Xenobiotics	GSTP1; CYP1B1
by Cytochrome p450
Methane Metabolism	PRDX6; PRDX1
Phenylalanine Metabolism	PRDX6; PRDX1
Propanoate Metabolism	ALDH1A1; LDHA
Selenoamino Acid	PRMT5; AHCY
Metabolism
Sphingolipid Metabolism	SPHK1; SPHK2
Aminophosphonate	PRMT5
Metabolism
Androgen and Estrogen	PRMT5
Metabolism
Ascorbate and Aldarate	ALDH1A1
Metabolism
Bile Acid Biosynthesis	ALDH1A1
Cysteine Metabolism	LDHA
Fatty Acid Biosynthesis	FASN
Glutamate Receptor	GNB2L1
Signaling
NRF2-mediated Oxidative	PRDX1
Stress Response
Pentose Phosphate Pathway	GPI
Pentose and Glucuronate	UCHL1
Interconversions
Retinol Metabolism	ALDH1A1
Riboflavin Metabolism	TYR
Tyrosine Metabolism	PRMT5, TYR
Ubiquinone Biosynthesis	PRMT5
Valine, Leucine and	ALDH1A1
Isoleucine Degradation
Glycine, Serine and	CHKA
Threonine Metabolism
Lysine Degradation	ALDH1A1
Pain/Taste	TRPM5; TRPA1
Pain	TRPM7; TRPC5; TRPC6; TRPC1; Cnr1; cnr2; Grk2; Trpa1; Pomc;
	Cgrp; Crf; Pka; Era; Nr2b; TRPM5; Prkaca; Prkacb; Prkar1a;
	Prkar2a
Mitochondrial Function	AIF; CytC; SMAC (Diablo); Aifm-1; Aifm-2
Developmental Neurology	BMP-4; Chordin (Chrd); Noggin (Nog); WNT (Wnt2; Wnt2b,
	Wnt3a, Wnt4; Wnt5a; Wnt6; Wnt7b; Wnt8b; Wnt9a; Wnt9b;
	Wnt10a; Wnt10b, Wnt16); beta-catenin; Dkk-1; Frizzled
	related proteins; Otx-2; Gbx2; FGF-8; Reelin; Dab1; unc-86
	(Pou4f1 or Brn3a); Numb; Rein

TABLE 4

INDICATION(S)	THERAPEUTIC PROTEIN

Maple syrup urine disease	3-methyl-2-oxobutanoate dehydrogenase
Medium-chain acyl-CoA	Acyl-CoA dehydrogenase
dehydrogenase deficiency
Alpha 1-antitrypsin deficiency	Alpha 1 protease inhibitor
Pompe disease	Alpha glucosidase
Paroxysmal nocturnal	Anti-complement factor C5 Mab
hemoglobinuria
Familial dysbetalipoproteinemia	Apolipoprotein E
Argininemia	Arginase
Argininosuccinic acidemia	Argininosuccinate lyase
Citrullinemia, type I	Argininosuccinate synthase
Short-chain acyl-CoA	Butyryl-CoA dehydrogenase
dehydrogenase deficiency
Hereditary angioedema	C1 esterase inhibitor
Carbamylphosphate synthetase	Carbamylphosphate synthetase
deficiency
Cystic fibrosis	CFTR
Hemophilia B	Factor IX
Hemophilia A, Hemophilia B	Factor VII
Hemophilia A	Factor VIII
Classical galactosemia	Galactose-1-phosphate uridylyltransferase
von Gierke's disease	Glucose-6-phosphatase
Glutaric acidemia, type I	Glutaryl-CoA dehydrogenase
Isovaleric aciduria	Isovaleric acid CoA dehydrogenase deficiency
Homozygous familial	LDL receptor
hypercholesterolemia
Long-chain 3-OH acyl-CoA	Long-chain-3-hydroxyacyl-CoA dehydrogenase
dehydrogenase deficiency
Very long-chain acyl-CoA	Long-chain-acyl-CoA dehydrogenase
dehydrogenase deficiency
Methylmalonyl-CoA mutase	Methylmalonyl-CoA mutase
deficiency
Ornithine transcarbamylase	Ornithine transcarbamylase
deficiency
Phenylketonuria	Phenylalanine hydroxylase
Acute intermittent porphyria	Porphobilinogen deaminase
Propionic acidemia	Propionyl-CoA carboxylase
Hyperoxaluria, type I	Serine-pyruvate aminotransferase
Crigler-Najjar syndrome	UDP-glucuronosyltransferase
Non-Hodgkin lymphoma	Anti-CD20 mAb
Allergic asthma	Anti-IgE mAb
Psoriasis	Anti-IL-12 & IL-23 mAb
Rheumatoid arthritis	Anti-interleukin-6 (IL-6) mAb
Anemia	Erythropoietin
Rheumatoid arthritis	T-cell costimulation blocker
Rheumatoid arthritis	TNF-alpha inhibitors (including anti-TNF-alpha mAb)
Gout	Urate oxidase
Familial chylomicronemia	Lipoprotein lipase
Melanoma	Anti-CTLA4 mAb
Head and neck cancer, Metastatic	Anti-EGFr mAb
colorectal cancer
HER2+ breast cancer, gastric	Anti-HER2 mAb
cancer
Metastatic colorectal cancer,	Anti-VEGF mAb
NSCLC, others
Blepharospasm, Cervical	Botulinum toxin
dystonia, Chronic migraine, more
Female infertility	Follicle stimulating hormone
Type 2 diabetes mellitus	Glucagon-like peptide 1 (GLP-1) agonist
Growth hormone deficiency	Growth hormone 1/Growth hormone 2
Type 2 diabetes mellitus	Insulin
Hypoparathyroidism	Parathyroid hormone
Asthma	SERCA2
Asthma	FoxP3
Surfactant Deficiency	Pulmonary surfactants (SFTPA1, SFTPB, SFTPC, SFTPD)
Pulmonary Alveolar proteinosis	GM-CSF Receptor (CSF2RA, CSF2RB)
alport syndrome	Col4A5
Stargardt's Disease	ABCA4
Retinitis pigmentosa	Rhodopsins
Adrenoleukodystrophy	ABCD1
Adenosine deaminase deficiency	Adenosine deaminase
Familial adenomatous polyposis	APC
Autosomal recessive polycystic	ARPKD
kidney disease
Metachromatic leukodystrophy	Arylsulfatase A
Batten disease	Battenin + others
Beta-thalassemia	Beta globin
X-linked agammaglobulinemia	Bruton's tyrosine kinase
Becker muscular dystrophy	Dystrophin
Duchenne muscular dystrophy	Dystrophin
Marfan syndrome	FBN1
Fragile X syndrome	FMRP
Krabbe disease	Galactocerebrosidase
Sickle cell disease	Hemoglobin
Sanfilippo syndrome, type A	Heparan N-sulfatase
(MPS IIIA)
GM2 gangliosidosis	HEXA, HEXB
Hemachromatosis	HFE protein
Huntington disease	Huntingtin
Lesch-Nyhan syndrome	Hypoxanthine phosphoribosyltransferase 1
McArdle disease	Muscle glycogen phosphorylase
Sanfilippo syndrome, type B	N-acetyl-alpha-D-glucosaminidase
(MPS IIIB)
Leber's hereditary optic	NADH dehydrogenase
neuropathy
Neurofibromatosis, type 1	NF-1
Niemann Pick disease, type C	NPC1
Alpers disease	POLG
Von Hippel-Lindau disease	pVHL
Paget disease of bone	Sequestosome 1
Carnitine uptake defect	SLC22A5
Cystinuria	SLC7A9
Niemann Pick disease, type A/B	SMPD1
Spinal muscular atrophy	Survival motor neuron protein
Li-Fraumeni syndrome	TP53
Fabry disease	Alpha galactosidase
Alpha-mannosidosis	Alpha-D-mannosidase
Hurler syndrome (MPS I)	Alpha-L iduronidase
Hemolytic uremic syndrome	Anti-complement factor C5 mAb
Morquio syndrome, type B	Beta-galactosidase
(MPS IVB)
Multiple carboxylase deficiency	Biotin-methylcrotonoyl-CoA-carboxylase ligase
Homocystinuria	Cystathionine beta-synthase
Cystinosis	Cystinosin
Cystic fibrosis	Deoxyribonuclease I
Erythropoietic protoporphyria	Ferrochelatase
Tyrosinemia, type I	Fumarylacetoacetase
GALK deficiency	Galactokinase
Morquio syndrome, type A	Galactose 6-sulfate sulfatase
(MPS IVA)
GALE deficiency	Galactose epimerase
Gaucher disease	Glucocerebrosidase
Alkaptonuria	Homogentisate 1,2-dioxygenase
Hunter syndrome (MPS II)	Iduronate-2-sulfatase
Lysosomal acid lipase deficiency	Lysosomal acid lipase
Hypermethioninemia	Methionine adenosyltransferase
3-Methylcrotonyl-CoA	Methylcrotonoyl-CoA carboxylase
carboxylase deficiency
3-Methylglutaconic aciduria	Methylglutaconyl-CoA hydratase
Maroteaux-Lamy syndrome	N-acetylgalactosamine 4-sulfatase
(MPS VI)
Familial mediterranean fever	Pyrin (MEFV)
Tetrahydrobiopterin-deficient	Tetrahydrobiopterin
hyperphenylalaninemia
Juvenile rheumatoid arthritis	TNF-alpha inhibitors
Psoriatic arthritis	TNF-alpha inhibitors
Hypophosphatasia	TNSALP
Gilbert syndrome	UDP-glucuronosyltransferase
Porphyria cutanea tarda	Uroporphyrinogen decarboxylase
Wilson disease	Wilson disease protein
Systemic lupus erythematosus	Anti-BAFF
Osteoporosis	Anti-RANKL mAb
Multiple sclerosis	Anti-VLA-4 mAb
Neutropenia	G-CSF
Immunoglobulin deficiency	Immunoglobulin
Primary humoral immune	Immunoglobulin
deficiencies (e.g., CVID)
Infectious diseases vaccines	Infectious antigen
Hepatitis B, Hepatitis C	Interferon alpha
Multiple sclerosis	Interferon beta
Chronic immune	Thrombopoietin
thrombocytopenia
Ehlers-Danlos syndrome, type 1	Proteins encoded by ADAMTS2, B3GALT6, B4GALT7,
	CHST14, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2,
	DSE, FKBP14, PLOD1, PRDM5, SLC39A13, TNXB, and
	ZNF469
Stickler syndrome	Proteins encoded by COL11A1, COL11A2, COL2A1,
	COL9A1, COL9A2, and COL9A3
Hereditary hemorrhagic	Proteins encoded by ACVRL1, ENG, and SMAD4
telangiectasia
Hereditary spherocytosis	Proteins encoded by ANK1, EPB42, SLC4A1, SPTA1 and
	SPTB
Brugada syndrome	Proteins encoded by CACNA1C, CACNA2D1, CACNB2,
	GPD1L, HCN4, KCND3, KCNE3, KCNE5, KCNJ8, RANGRF,
	SCN1B, SCN2B, SCN3B, SCN5A, SLMAP, and TRPM4
Osteopetrosis	Proteins encoded by CA2, CLCN7, IKBKG, ITGB3, OSTM1,
	PLEKHM1, TCIRG1, TNFRSF11A, and TNFSF11
Mitochondrial oxidative	Proteins encoded by FBXL4, and NDUFB9
phosphorylation disorders

TABLE 5

INDICATION(S)	THERAPEUTIC PROTEIN	GENE

Achromatopsia type
2	Cyclic nucleotide-gated channel,	CNGA3
	α3 subunit
Achromatopsia type 3	Cyclic nucleotide-gated channel,	CNGB3
	β3 subunit
Aland Island eye disease	Cav1.4: calcium channel, voltage-	CACNA1F
	gated, L type, α1F subunit
Andersen-Tawil syndrome	Kir2.1: potassium channel,	KCNJ2
	inwardly-rectifying, subfamily J,
	member 2
Benign familial infantile epilepsy	Nav2.1: sodium channel, voltage-	SCN2A
	gated, type II, α subunit
	Kv7.2: potassium channel,	KCNQ2
	voltage-gated, KQT-like subfamily,
	member 2
	Kv7.3: potassium channel,	KCNQ3
	voltage-gated, KQT-like subfamily,
	member 3
Bestrophinopathy, autosomal-	Bestrophin 1	BEST!
recessive
Central core disease	RyR1: ryanodine receptor 1	RYR1
Charcot-Marie-Tooth disease	Transient receptor potential	TRPV4
type 2C	cation channel, subfamily V,
	member 4
Childhood absence epilepsy	γ-aminobutyric acid A receptor,	GABRA1
	α1 subunit
	γ-aminobutyric acid A receptor,	GABRA6
	α6 subunit
	y-aminobutyric acid A receptor,	GABRB3
	β3 subunit
	γ-aminobutyric acid A receptor, γ2	GABRG2
	subunit

Cav3.2: calcium channel, voltage-gated, T type, α1H subunit

CACNA1H

Cognitive impairment with or	Nav1.6: sodium channel, voltage-	SCN8A
without cerebellar ataxia	gated, type VIII, α subunit
Cone-rod dystropy, X-linked,	Cav1.4: calcium channel, voltage-	CACNAlF
type 3	gated, L type, α1F subunit
Congenital distal spinal muscular	Transient receptor potential	TRPV4
atrophy	cation channel, subfamily V,
	member 4
Congenital indifference to pain,	Nav1.7: Sodium channel, voltage-	SCN9A
autosomal-recessive	gated, type IX, α subunit
Congenital myasthenic syndrome	Cholinergic receptor, muscle	CHRNA1
	nicotinic, α1 subunit
	Cholinergic receptor, muscle	CHRNB1
	nicotinic, β1 subunit
	Cholinergic receptor, muscle	CHRND
	nicotinic, δ subunit
	Cholinergic receptor, muscle	CHRNE
	nicotinic, ε subunit
	Nav1.4: sodium channel, voltage-	SCN4A
	gated, type IV, α subunit
Congenital stationary night	Transient receptor potential	TRPM1
blindness type 1C	cation channel, subfamily M,
	member 1
Congenital stationary night	Cav1.4: calcium channel, voltage-	CACNA1F
blindness type 2A	gated, L type, α1F subunit
Deafness, autosomal-dominant,	Kv7.4: potassium channel,	KCNQ4
type 2A	voltage-gated, KQT-like subfamily,
	member 4
Deafness, autosomal-recessive,	Kir4.1: potassium channel,	KCNJ10
type 4, with enlarged	inwardly-rectifying, subfamily J,
vestibular aqueduct	member 10
Dravet syndrome	Nav1.1: sodium channel, voltage-	SCN1A
	gated, type I, α subunit
	y-aminobutyric acid A receptor, γ2	GABRG2
	subunit
Early infantile epileptic	Kv7.2: potassium channel,	KCNQ2
encephalopathy type 7	voltage-gated, KQT-like subfamily,
	member 2
Early infantile epileptic	Nav2.1: sodium channel, voltage-	SCN2A
encephalopathy type 11	gated, type II, α subunit
Early infantile epileptic	Nav1.6: sodium channel, voltage-	SCN8A
encephalopathy type 13	gated, type VIII, α subunit
Early infantile epileptic	KCa4.1: potassium channel,	KCNT1
encephalopathy type 14	subfamily T, member 1
EAST/SeSAME syndrome	Kir4.1: potassium channel,	KCNJ10
	inwardly-rectifying, subfamily J,
	member 10
Episodic ataxia type 1	Kv1.1: potassium channel,	KCNA1
	voltage-gated, shaker-related
	subfamily, member 1
Episodic ataxia type 2	Cav2.1: calcium channel, voltage-	CACNA1A
	gated, P/Q type, α1A subunit
Episodic ataxia type 5	Cavβ4: calcium channel, voltage-	CACNB4
	gated, β4 subunit
Familial episodic pain syndrome	Transient receptor potential	TRPA1
	cation channel, subfamily A,
	member 1
Familial hemiplegic migraine	Cav2.1: calcium channel, voltage-	CACNA1A
type 1	gated, P/Q type, α1A subunit
Familialhemiplegic migraine	Navtl: sodium channel, voltage-	SCN1A
type 3	gated, type I, α subunit
Generalized epilepsy with febrile	NavI31: sodium channel, voltage-	SCN1B
seizures plus (GEFS+)	gated, type I, β subunit
	Nav1.1: sodium channel, voltage-	SCN1A
	gated, type I, α subunit
	γ-aminobutyric acid A receptor, γ2	GABRG2
	subunit
Generalized epilepsy with	KCa1.1: potassium channel,	KCNMA1
paroxysmal dyskinesia	calcium-activated, large
	conductance, subfamily M,
	α1 subunit
Hereditary hyperekplexia	Glycine receptor, α1 subunit	GLRA1
	Glycine receptor, β subunit	GLRB
Hyperkalemic periodic paralysis	Nav1.4: sodium channel, voltage-	SCN4A
	gated, type IV, α subunit
Hypokalemic periodic paralysis	Cav1.1: calcium channel, voltage-	CACNAlS
type 1	gated, L type, α1S subunit
Hypokalemic periodic paralysis	Nav1.4: sodium channel, voltage-	SCN4A
type 2	gated, type IV, α subunit
Juvenile macular degeneration	Cyclic nucleotide-gated channel,	CNGB3
	β3 subunit
Juvenile myoclonic epilepsy	γ-aminobutyric acid A receptor,	GABRA1
	α1 subunit
	Cavβ4: calcium channel, voltage-	CACNB4
	gated, β4 subunit
Malignant hyperthermia	RyR1: ryanodine receptor 1	RYR1
susceptibility	Cav1.1: calcium channel, voltage-	CACNA1S
	gated, L type, α1S subunit
Mucolipidosis type IV	TRPN1L1/mucolipin 1	MCOLN1
Multiple pterygium syndrome,	Cholinergic receptor, muscle	CHRNA1
lethal type	nicotinic, α1 subunit
Multiple pterygium syndrome,	Cholinergic receptor, muscle	CHRND
nonlethal type (Escobar variant)	nicotinic, δ subunit
	Cholinergic receptor, muscle	CHRNG
	nicotinic, γ subunit
Myotonia congenita, autosomal-	CIC-1: chloride channel 1, voltage-	CLCN1
dominant (Thomsen disease)	gated
Myotonia congenita, autosomal-	CIC-1: chloride channel 1, voltage-	CLCN1
recessive (Becker disease)	gated
Nocturnal frontal lobe epilepsy	Cholinergic receptor, neuronal	CHRNA4
type 1	nicotinic, α4 subunit
Nocturnal frontal lobe epilepsy	Cholinergic receptor, neuronal	CHRNB2
type 3	nicotinic, β2 subunit
Nocturnal frontal lobe epilepsy	Cholinergic receptor, neuronal	CHRNA2
type 4	nicotinic, α2 subunit
Nocturnal frontal lobe epilepsy	KCa4.1: potassium channel,	KCNT1
type 5	subfamily T, member 1
Paramyotonia congenita	Nav1.4: sodium channel, voltage-	SCN4A
	gated, type IV, α subunit
Paroxysmal extreme pain disorder	Nav1.7: Sodium channel voltage-	SCN9A
	gated, type IX, α subunit
Potassium-aggravated myotonia	Nav1.4: sodium channel, voltage-	SCN4A
	gated, type IV, α subunit
Primary erythermalgia	Nav1.7: sodium channel, voltage-	SCN9A
	gated, type IX, α subunit
Retinitis pigmentosa type 45,	Cyclic nucleotide-gated channel,	CNGB1
autosomal-recessive	β1 subunit
Retinitis pigmentosa type 49,	Cyclic nucleotide-gated channel,	CNGA1
autosomal-recessive	al subunit
Retinitis pigmentosa type 50,	Bestrophin 1	BEST1
autosomal-dominant
Scapuloperoneal spinal muscular	Transient receptor potential	TRPV4
atrophy	cation channel, subfamily V,
	member 4
Small fiber neuropathy	Nav1.7: sodium channel, voltage-	SCN9A
	gated, type IX, α subunit
Spinocerebellar ataxia type 6	Cav2.1: calcium channel, voltage-	CACNA1A
	gated, P/Q type, α1A subunit
Spinocerebellar ataxia type 13	Kv3.3: potassium channel,	KCNC3
	voltage-gated, Shaw-related
	subfamily, member 3
Vitelliform macular dystrophy	Bestrophin 1	BEST1
Vitreoretinochoroidopathy	Bestrophin 1	BEST1

TABLE 6

Secreted Proteins

Uniprot
ID	Protein Name	Gene Name

A1E959	Odontogenic ameloblast-associated protein	ODAM
A1KZ92	Peroxidasin-like protein	PXDNL
A1L453	Serine protease 38	PRSS38
A1L4H1	Soluble scavenger receptor cysteine-rich domain-containing	SSC5D
	protein SSC5D
A2RUU4	Colipase-like protein 1	CLPSL1
A2VDF0	Fucose mutarotase	FUOM
A2VEC9	SCO-spondin	SSPO
A3KMH1	von Willebrand factor A domain-containing protein 8	VWA8
A4D0S4	Laminin subunit beta-4	LAMB4
A4D1T9	Probable inactive serine protease 37	PRSS37
A5D8T8	C-type lectin domain family 18 member A	CLEC18A
A6NC86	phospholipase A2 inhibitor and Ly6/PLAUR domain-	PINLYP
	containing protein
A6NCI4	von Willebrand factor A domain-containing protein 3A	VWA3A
A6ND01	Probable folate receptor delta	FOLR4
A6NDD2	Beta-defensin 108B-like
A6NE02	BTB/POZ domain-containing protein 17	BTBD17
A6NEF6	Growth hormone 1	GH1
A6NF02	NPIP-like protein L00730153
A6NFB4	HCG1749481, isoform CRA_k	CSH1
A6NFZ4	Protein FAM24A	FAM24A
A6NG13	Glycosyltransferase 54 domain-containing protein
A6NGN9	IgLON family member 5	IGLON5
A6NHN0	Otolin-1	OTOL1
A6NHN6	Nuclear pore complex-interacting protein-like 2	NPIPL2
A6NI73	Leukocyte immunoglobulin-like receptor subfamily A	LILRA5
	member 5
A6NIT4	Chorionic somatomammotropin hormone 2 isoform 2	CSH2
A6NJ69	IgA-inducing protein homolog	IGIP
A6NKQ9	Choriogonadotropin subunit beta variant 1	CGB1
A6NMZ7	Collagen alpha-6(VI) chain	COL6A6
A6NNS2	Dehydrogenase/reductase SDR family member 7C	DHRS7C
A6XGL2	Insulin A chain	INS
A8K0G1	Protein Wnt	WNT7B
A8K2U0	Alpha-2-macroglobulin-like protein 1	A2ML1
A8K7I4	Calcium-activated chloride channel regulator 1	CLCA1
A8MTL9	Serpin-like protein HMSD	HMSD
A8MV23	Serpin E3	SERPINE3
A8MZH6	Oocyte-secreted protein 1 homolog	OOSP1
A8TX70	Collagen alpha-5(VI) chain	COL6A5
B0ZBE8	Natriuretic peptide	NPPA
B1A4G9	Somatotropin	GH1
B1A4H2	HCG1749481, isoform CRA_d	CSH1
B1A4H9	Chorionic somatomammotropin hormone	CSH2
B1AJZ6	Protein Wnt	WNT4
B1AKI9	Isthmin-1	ISM1
B2RNN3	Complement C1q and tumor necrosis factor-related protein 9B	C1QTNF9B
B2RUY7	von Willebrand factor C domain-containing protein 2-like	VWC2L
B3GU2	Prostate and testis expressed protein 3	PATE3
B4D103	SEC11-like 3 (S. cerevisiae), isoform CRA_a	SEC11L3
B4DJF9	Protein Wnt	WNT4
B4DUL4	SEC11-like 1 (S. cerevisiae), isoform CRA_d	SEC11L1
B5MCC8	Protein Wnt	WNT106
B8A595	Protein Wnt	WNT7B
B8A597	Protein Wnt	WNT7B
B8A598	Protein Wnt	WNT7B
B9A064	Immunoglobulin lambda-like polypeptide 5	IGLL5
C9J3H3	Protein Wnt	WNT106
C9J8I8	Protein Wnt	WNT5A
C9JAF2	Insulin-like growth factor II Ala-25 Del	IGF2
C9JCI2	Protein Wnt	WNT106
C9JL84	HERV-H LTR-associating protein 1	HHLA1
C9JNR5	Insulin A chain	INS
C9JUI2	Protein Wnt	WNT2
D6RF47	Protein Wnt	WNT8A
D6RF94	Protein Wnt	WNT8A
E2RYF7	Protein PBMUCL2	HCG22
E5RFR1	PENK(114-133)	PENK
E7EML9	Serine protease 44	PRSS44
E7EPC3	Protein Wnt	WNT96
E7EVP0	Nociceptin	PNOC
E9PD02	Insulin-like growth factor I	IGF1
E9PH60	Protein Wnt	WNT16
E9PJL6	Protein Wnt	WNT11
F5GYM2	Protein Wnt	WNT56
F5H034	Protein Wnt	WNT56
F5H364	Protein Wnt	WNT56
F5H7Q6	Protein Wnt	WNT56
F8WCM5	Protein INS-IGF2	INS-IGF2
F8WDR1	Protein Wnt	WNT2
H0Y663	Protein Wnt	WNT4
H0YK72	Signal peptidase complex catalytic subunit SEC11A	SEC11A
H0YK83	Signal peptidase complex catalytic subunit SEC11A	SEC11A
H0YM39	Chorionic somatomammotropin hormone	CSH2
H0YMT7	Chorionic somatomammotropin hormone	CSH1
H0YN17	Chorionic somatomammotropin hormone	CSH2
H0YNA5	Signal peptidase complex catalytic subunit SEC11A	SEC11A
H0YNG3	Signal peptidase complex catalytic subunit SEC11A	SEC11A
H0YNX5	Signal peptidase complex catalytic subunit SEC11A	SEC11A
H7BZ68	Protein Wnt	WNT10A
H9KV56	Choriogonadotropin subunit beta variant 2	CGB2
I3L0L8	Protein Wnt	WNT96
J3KNZ1	Choriogonadotropin subunit beta variant 1	CGB1
J3KP00	Choriogonadotropin subunit beta	CGB7
J30T02	Choriogonadotropin subunit beta variant 1	CGB1
O00175	C—C motif chemokine 24	CCL24
O00182	Galectin-9	LGALS9
O00187	Mannan-binding lectin serine protease 2	MASP2
O00230	Cortistatin	CORT
O00253	Agouti-related protein	AGRP
O00270	12-(S)-hydroxy-5,8,10,14-eicosatetraenoic acid receptor	GPR31
O00292	Left-right determination factor 2	LEFTY2
O00294	Tubby-related protein 1	TULP1
O00295	Tubby-related protein 2	TULP2
O00300	Tumor necrosis factor receptor superfamily member 11B	TNFRSF11B
O00339	Matrilin-2	MATN2
O00391	Sulfhydryl oxidase 1	QS0X1
O00468	Agrin	AGRN
O00515	Ladinin-1	LAD1
O00533	Processed neural cell adhesion molecule L1-like protein	CHL1
O00584	Ribonuclease T2	RNASET2
O00585	C—C motif chemokine 21	CCL21
O00602	Ficolin-1	FCN1
O00622	Protein CYR61	CYR61
O00626	MDC(5-69)	CCL22
O00634	Netrin-3	NTN3
O00744	Protein Wnt-10b	WNT10B
O00755	Protein Wnt-7a	WNT7A
O14498	Immunoglobulin superfamily containing leucine-rich repeat	ISLR
	protein
O14511	Pro-neuregulin-2, membrane-bound isoform	NRG2
O14594	Neurocan core protein	NCAN
O14625	C—X—C motif chemokine 11	CXCL11
O14638	Ectonucleotide pyrophosphatase/phosphodiesterase family	ENPP3
	member 3
O14656	Torsin-1A	TOR1A
O14657	Torsin-1B	TOR1B
O14786	Neuropilin-1	NRP1
O14788	Tumor necrosis factor ligand superfamily member 11,	TNFSF11
	membrane form
O14791	Apolipoprotein L1	APOL1
O14793	Growth/differentiation factor 8	MSTN
O14904	Protein Wnt-9a	WNT9A
O14905	Protein Wnt-9b	WNT9B
O14944	Proepiregulin	EREG
O14960	Leukocyte cell-derived chemotaxin-2	LECT2
O15018	Processed PDZ domain-containing protein 2	PDZD2
O15041	Semaphorin-3E	SEMA3E
O15072	A disintegrin and metalloproteinase with thrombospondin	ADAMTS3
	motifs 3
O15123	Angiopoietin-2	ANGPT2
O15130	Neuropeptide FF	NPFF
O15197	Ephrin type-B receptor 6	EPHB6
O15204	ADAM DEC1	ADAMDEC1
O15230	Laminin subunit alpha-5	LAMA5
O15232	Matrilin-3	MATN3
O15240	Neuroendocrine regulatory peptide-1	VGF
O15263	Beta-defensin 4A	DEFB4A
O15335	Chondroadherin	CHAD
O15393	Transmembrane protease serine 2 catalytic chain	TMPRSS2
O15444	C—C motif chemokine 25	CCL25
O15467	C—C motif chemokine 16	CCL16
O15496	Group 10 secretory phospholipase A2	PLA2G10
O15520	Fibroblast growth factor 10	FGF10
O15537	Retinoschisin	RS1
O43157	Plexin-B1	PLXNB1
O43184	Disintegrin and metalloproteinase domain-containing	ADAM12
	protein 12
O43240	Kallikrein-10	KLK10
O43278	Kunitz-type protease inhibitor 1	SPINT1
O43320	Fibroblast growth factor 16	FGF16
O43323	Desert hedgehog protein C-product	DHH
O43405	Cochlin	COCH
O43508	Tumor necrosis factor ligand superfamily member 12,	TNFSF12
	membrane form
O43555	Progonadoliberin-2	GNRH2
O43557	Tumor necrosis factor ligand superfamily member 14,	TNFSF14
	soluble form
O43692	Peptidase inhibitor 15	PI15
O43699	Sialic acid-binding Ig-like lectin 6	SIGLEC6
O43820	Hyaluronidase-3	HYAL3
O43827	Angiopoietin-related protein 7	ANGPTL7
O43852	Calumenin	CALU
O43854	EGF-like repeat and discoidin l-like domain-containing	EDIL3
	protein 3
O43866	CD5 antigen-like	CD5L
O43897	Tolloid-like protein 1	TLL1
O43915	Vascular endothelial growth factor D	FIGF
O43927	C—X—C motif chemokine 13	CXCL13
O60218	Aldo-keto reductase family 1 member B10	AKR1B10
O60235	Transmembrane protease serine 11D	TMPRSS11D
O60258	Fibroblast growth factor 17	FGF17
O60259	Kallikrein-8	KLK8
O60383	Growth/differentiation factor 9	GDF9
O60469	Down syndrome cell adhesion molecule	DSCAM
O60542	Persephin	PSPN
O60565	Gremlin-1	GREM1
O60575	Serine protease inhibitor Kazal-type 4	SPINK4
O60676	Cystatin-8	CST8
O60687	Sushi repeat-containing protein SRPX2	SRPX2
O60844	Zymogen granule membrane protein 16	ZG16
O60882	Matrix metalloproteinase-20	MMP20
O60938	Keratocan	KERA
O75015	Low affinity immunoglobulin gamma Fc region receptor III-B	FCGR3B
O75077	Disintegrin and metalloproteinase domain-containing	ADAM23
	protein 23
O75093	Slit homolog 1 protein	SLIT1
O75094	Slit homolog 3 protein	ALIT3
O75095	Multiple epidermal growth factor-like domains protein 6	MEGF6
O75173	A disintegrin and metalloproteinase with thrombospondin	ADAMTS4
	motifs 4
O75200	Nuclear pore complex-interacting protein-like 1	NPIPL1
O75339	Cartilage intermediate layer protein 1 C1	CILP
O75354	Ectonucleoside triphosphate diphosphohydrolase 6	ENTPD6
O75386	Tubby-related protein 3	TULP3
O75398	Deformed epidermal autoregulatory factor 1 homolog	DEAF1
O75443	Alpha-tectorin	TECTA
O75445	Usherin	USH2A
O75462	Cytokine receptor-like factor 1	CRLF1
O75487	Glypican-4	GPC4
O75493	Carbonic anhydrase-related protein 11	CA11
O75594	Peptidoglycan recognition protein 1	PGLYRP1
O75596	C-type lectin domain family 3 member A	CLEC3A
O75610	Left-right determination factor 1	LEFTY1
O75629	Protein CREG1	CREG1
O75636	Ficolin-3	FCN3
O75711	Scrapie-responsive protein 1	SCRG1
O75715	Epididymal secretory glutathione peroxidase	GPX5
O75718	Cartilage-associated protein	CRTAP
O75829	Chondrosurfactant protein	LECT1
O75830	Serpin I2	AERPINI2
O75882	Attractin	ATRN
O75888	Tumor necrosis factor ligand superfamily member 13	TNFSF13
O75900	Matrix metalloproteinase-23	MMP23A
O75951	Lysozyme-like protein 6	LYZL6
O75973	C1q-related factor	C1QL1
O76038	Secretagogin	SCGN
O76061	Stanniocalcin-2	STC2
O76076	WNT1-inducible-signaling pathway protein 2	WISP2
O76093	Fibroblast growth factor 18	FGF18
O76096	Cystatin-F	CST7
O94769	Extracellular matrix protein 2	ECM2
O94813	Slit homolog 2 protein C-product	ALIT2
O94907	Dickkopf-related protein 1	DKK1
O94919	Endonuclease domain-containing 1 protein	ENDOD1
O94964	N-terminal form	SOGA1
O95025	Semaphorin-3D	SEMA3D
O95084	Serine protease 23	PRSS23
O95150	Tumor necrosis factor ligand superfamily member 15	TNFSF15
O95156	Neurexophilin-2	NXPH2
O95157	Neurexophilin-3	NXPH3
O95158	Neurexophilin-4	NXPH4
O95388	WNT1-inducible-signaling pathway protein 1	WISP1
O95389	WNT1-inducible-signaling pathway protein 3	WI5P3
O95390	Growth/differentiation factor 11	GDF11
O95393	Bone morphogenetic protein 10	BMP10
O95399	Urotensin-2	UTS2
O95407	Tumor necrosis factor receptor superfamily member 6B	TNFRSF6B
O95428	Papilin	PAPLN
O95445	Apolipoprotein M	APOM
O95450	A disintegrin and metalloproteinase with thrombospondin	ADAMTS2
	motifs 2
O95460	Matrilin-4	MATN4
O95467	LHAL tetrapeptide	GNAS
O95631	Netrin-1	NTN1
O95633	Follistatin-related protein 3	FSTL3
O95711	Lymphocyte antigen 86	LY86
O95715	C—X—C motif chemokine 14	CXCL14
O95750	Fibroblast growth factor 19	FGF19
O95760	Interleukin-33	IL33
O95813	Cerberus	CER1
O95841	Angiopoietin-related protein 1	ANGPTL1
O95897	Noelin-2	OLFM2
O95925	Eppin	EPPIN
O95965	Integrin beta-like protein 1	ITGBL1
O95967	EGF-containing fibulin-like extracellular matrix protein 2	EFEMP2
O95968	Secretoglobin family 1D member 1	SCGB1D1
O95969	Secretoglobin family 1D member 2	SCGB1D2
O95970	Leucine-rich glioma-inactivated protein 1	LGI1
O95972	Bone morphogenetic protein 15	BMP15
O95994	Anterior gradient protein 2 homolog	AGR2
O95998	Interleukin-18-binding protein	IL18BP
O96009	Napsin-A	NAPSA
O96014	Protein Wnt-11	WNT11
P00450	Ceruloplasmin	CP
P00451	Factor VIIIa light chain	F8
P00488	Coagulation factor XIII A chain	F13A1
P00533	Epidermal growth factor receptor	EGFR
P00709	Alpha-lactalbumin	LALBA
P00734	Prothrombin	F2
P00738	Haptoglobin beta chain	HP
P00739	Haptoglobin-related protein	HPR
P00740	Coagulation factor IXa heavy chain	F9
P00742	Factor X heavy chain	F10
P00746	Complement factor D	CFD
P00747	Plasmin light chain B	PLG
P00748	Coagulation factor XIIa light chain	F12
P00749	Urokinase-type plasminogen activator long chain A	PLAU
P00750	Tissue-type plasminogen activator	PLAT
P00751	Complement factor B Ba fragment	CFB
P00797	Renin	REN
P00973	2′-5′-oligoadenylate synthase 1	OAS1
P00995	Pancreatic secretory trypsin inhibitor	SPINK1
P01008	Antithrombin-III	SERPINC1
P01009	Alpha-1-antitrypsin	SERPINA1
P01011	Alpha-1-antichymotrypsin His-Pro-less	SERPINA3
P01019	Angiotensin-1	AGT
P01023	Alpha-2-macroglobulin	A2M
P01024	Acylation stimulating protein	C3
P01031	Complement C5 beta chain	C5
P01033	Metalloproteinase inhibitor 1	TIMP1
P01034	Cystatin-C	CST3
P01036	Cystatin-S	CST4
P01037	Cystatin-SN	CST1
P01042	Kininogen-1 light chain	KNG1
P01127	Platelet-derived growth factor subunit B	PDGFB
P01135	Transforming growth factor alpha	TGFA
P01137	Transforming growth factor beta-1	TGFB1
P01138	Beta-nerve growth factor	NGF
P01148	Gonadoliberin-1	GNRH1
P01160	Atrial natriuretic factor	NPPA
P01178	Oxytocin	OXT
P01185	Vasopressin-neurophysin 2-copeptin	AVP
P01189	Corticotropin	POMC
P01210	PENK(237-258)	PENK
P01213	Alpha-neoendorphin	PDYN
P01215	Glycoprotein hormones alpha chain	CGA
P01222	Thyrotropin subunit beta	TSHB
P01225	Follitropin subunit beta	FSHB
P01229	Lutropin subunit beta	LHB
P01233	Choriogonadotropin subunit beta	CGB8
P01236	Prolactin	PRL
P01241	Somatotropin	GH1
P01242	Growth hormone variant	GH2
P01243	Chorionic somatomammotropin hormone	CSH2
P01258	Katacalcin	CALCA
P01266	Thyroglobulin	TG
P01270	Parathyroid hormone	PTH
P01275	Glucagon	GCG
P01282	Intestinal peptide PHM-27	VIP
P01286	Somatoliberin	GHRH
P01298	Pancreatic prohormone	PPY
P01303	C-flanking peptide of NPY	NPY
P01308	Insulin	INS
P01344	Insulin-like growth factor 11	IGF2
P01350	Big gastrin	GAST
P01374	Lymphotoxin-alpha	LTA
P01375	C-domain 1	TNF
P01562	Interferon alpha-1/13	IFNA1
P01563	Interferon alpha-2	IFNA2
P01566	Interferon alpha-10	IFNA10
P01567	Interferon alpha-7	IFNA7
P01568	Interferon alpha-21	IFNA21
P01569	Interferon alpha-5	IFNA5
P01570	Interferon alpha-14	IFNA14
P01571	Interferon alpha-17	IFNA17
P01574	Interferon beta	IFNB1
P01579	Interferon gamma	IFNG
P01583	Interleukin-1 alpha	ILIA
P01584	Interleukin-1 beta	IL1B
P01588	Erythropoietin	EPO
P01591	Immunoglobulin J chain	IGJ
P01732	T-cell surface glycoprotein CD8 alpha chain	CD8A
P01833	Polymeric immunoglobulin receptor	PIGR
P01857	Ig gamma-1 chain C region	IGHG1
P01859	Ig gamma-2 chain C region	IGHG2
P01860	Ig gamma-3 chain C region	IGHG3
P01861	Ig gamma-4 chain C region	IGHG4
P01871	Ig mu chain C region	IGHM
P01880	Ig delta chain C region	IGHD
P02452	Collagen alpha-1(I) chain	COL1A1
P02458	Chondrocalcin	COL2A1
P02461	Collagen alpha-1(III) chain	COL3A1
P02462	Collagen alpha-1(IV) chain	COL4A1
P02647	Apolipoprotein A-I	APOA1
P02649	Apolipoprotein E	APOE
P02652	Apolipoprotein A-II	APOA2
P02654	Apolipoprotein C-I	APOC1
P02655	Apolipoprotein C-II	APOC2
P02656	Apolipoprotein C-III	APOC3
P02671	Fibrinogen alpha chain	FGA
P02675	Fibrinopeptide B	FGB
P02679	Fibrinogen gamma chain	EGG
P02741	C-reactive protein	CRP
P02743	Serum amyloid P-component(1-203)	APCS
P02745	Complement C1q subcomponent subunit A	C1QA
P02746	Complement C1q subcomponent subunit B	C1QB
P02747	Complement C1q subcomponent subunit C	C1QC
P02748	Complement component C9b	C9
P02749	Beta-2-glycoprotein 1	APOH
P02750	Leucine-rich alpha-2-glycoprotein	LRG1
P02751	Ugl-Y2	FN1
P02753	Retinol-binding protein 4	RBP4
P02760	Trypstatin	AMBP
P02763	Alpha-1-acid glycoprotein 1	ORM1
P02765	Alpha-2-HS-glycoprotein chain A	AHSG
P02766	Transthyretin	TTR
P02768	Serum albumin	ALB
P02771	Alpha-fetoprotein	AFP
P02774	Vitamin D-binding protein	GC
P02775	Connective tissue-activating peptide III	PPBP
P02776	Platelet factor 4	PF4
P02778	CXCL10(1-73)	CXCL10
P02786	Transferrin receptor protein 1	TFRC
P02787	Serotransferrin	TF
P02788	Lactoferroxin-C	LTF
P02790	Hemopexin	HPX
P02808	Statherin	STATH
P02810	Salivary acidic proline-rich phosphoprotein 1/2	PRH2
P02812	Basic salivary proline-rich protein 2	PRB2
P02814	Peptide D1A	SMR3B
P02818	Osteocalcin	BGLAP
P03950	Angiogenin	ANG
P03951	Coagulation factor X1a heavy chain	F11
P03952	Plasma kallikrein	KLKB1
P03956	27 kDa interstitial collagenase	MMP1
P03971	Muellerian-inhibiting factor	AMH
P03973	Antileukoproteinase	SLPI
P04003	C4b-binding protein alpha chain	C4BPA
P04004	Somatomedin-B	VTN
P04054	Phospholipase A2	PLA2G1B
P04085	Platelet-derived growth factor subunit A	PDGFA
P04090	Relaxin A chain	RLN2
P04114	Apolipoprotein B-100	APOB
P04118	Colipase	CLPS
P04141	Granulocyte-macrophage colony-stimulating factor	CSF2
P04155	Trefoil factor 1	TFF1
P04180	Phosphatidylcholine-sterol acyltransferase	LCAT
P04196	Histidine-rich glycoprotein	HRG
P04217	Alpha-1B-glycoprotein	A1BG
P04275	von Willebrand antigen 2	VWF
P04278	Sex hormone-binding globulin	SHBG
P04279	Alpha-inhibin-31	SEMG1
P04280	Basic salivary proline-rich protein 1	PRB1
P04628	Proto-oncogene Wnt-1	WNT1
P04745	Alpha-amylase 1	AMY1A
P04746	Pancreatic alpha-amylase	AMY2A
P04808	Prorelaxin H1	RLN1
P05000	Interferon omega-1	IFNW1
P05013	Interferon alpha-6	IFNA6
P05014	Interferon alpha-4	IFNA4
P05015	Interferon alpha-16	IFNA16
P05019	Insulin-like growth factor I	IGF1
P05060	GAWK peptide	CHGB
P05090	Apolipoprotein D	APOD
P05109	Protein S100-A8	S100A8
P05111	Inhibin alpha chain	INHA
P05112	Interleukin-4	IL4
P05113	Interleukin-5	ILS
P05120	Plasminogen activator inhibitor 2	SERPINB2
P05121	Plasminogen activator inhibitor 1	SERPINE1
P05154	Plasma serine protease inhibitor	SERPINA5
P05155	Plasma protease C1 inhibitor	SERPING1
P05156	Complement factor I heavy chain	CFI
P05160	Coagulation factor XIII B chain	F136
P05161	Ubiquitin-like protein ISG15	ISG15
P05230	Fibroblast growth factor 1	FGF1
P05231	Interleukin-6	IL6
P05305	Big endothelin-1	EDN1
P05408	C-terminal peptide	SCG5
P05451	Lithostathine-1-alpha	REG1A
P05452	Tetranectin	CLEC3B
P05543	Thyroxine-binding globulin	SERPINA7
P05814	Beta-casein	CSN2
P05997	Collagen alpha-2(V) chain	COL5A2
P06276	Cholinesterase	BCHE
P06307	Cholecystokinin-12	CCK
P06396	Gelsolin	GSN
P06681	Complement C2	C2
P06702	Protein S100-A9	S100A9
P06727	Apolipoprotein A-IV	APOA4
P06734	Low affinity immunoglobulin epsilon Fc receptor soluble	FCER2
	form
P06744	Glucose-6-phosphate isomerase	GPI
P06850	Corticoliberin	CRH
P06858	Lipoprotein lipase	LPL
P06881	Calcitonin gene-related peptide 1	CALCA
P07093	Glia-derived nexin	SERPINE2
P07098	Gastric triacylglycerol lipase	LIPF
P07225	Vitamin K-dependent protein S	PROS1
P07237	Protein disulfide-isomerase	P4HB
P07288	Prostate-specific antigen	KLK3
P07306	Asialoglycoprotein receptor 1	ASGR1
P07355	Annexin A2	ANXA2
P07357	Complement component C8 alpha chain	C8A
P07358	Complement component C8 beta chain	C8B
P07360	Complement component C8 gamma chain	C8G
P07477	Alpha-trypsin chain 2	PRSS1
P07478	Trypsin-2	PRSS2
P07492	Neuromedin-C	GRP
P07498	Kappa-casein	CSN3
P07585	Decorin	DCN
P07911	Uromodulin	UMOD
P07942	Laminin subunit beta-1	LAMB1
P07988	Pulmonary surfactant-associated protein B	SFTPB
P07998	Ribonuclease pancreatic	RNASE1
P08118	Beta-microseminoprotein	MSMB
P08123	Collagen alpha-2(l) chain	COL1A2
P08185	Corticosteroid-binding globulin	SERPINA6
P08217	Chymotrypsin-like elastase family member 2A	CELA2A
P08218	Chymotrypsin-like elastase family member 2B	CELA2B
P08253	72 kDa type IV collagenase	MMP2
P08254	Stromelysin-1	MMP3
P08294	Extracellular superoxide dismutase [Cu-Zn]	SOD3
P08476	Inhibin beta A chain	INHBA
P08493	Matrix Gla protein	MGP
P08572	Collagen alpha-2(IV) chain	COL4A2
P08581	Hepatocyte growth factor receptor	MET
P08603	Complement factor H	CFH
P08620	Fibroblast growth factor 4	FGF4
P08637	Low affinity immunoglobulin gamma Fc region receptor III-A	FCGR3A
P08697	Alpha-2-antiplasmin	SERPINF2
P08700	Interleukin-3	IL3
P08709	Coagulation factor VII	F7
P08833	Insulin-like growth factor-binding protein 1	IGFBP1
P08887	Interleukin-6 receptor subunit alpha	IL6R
P08949	Neuromedin-B-32	NMB
P08F94	Fibrocystin	PKHD1
P09038	Fibroblast growth factor 2	FGF2
P09228	Cystatin-SA	CST2
P09237	Matrilysin	MMP7
P09238	Stromelysin-2	MMP10
P09341	Growth-regulated alpha protein	CXCL1
P09382	Galectin-1	LGALS1
P09466	Glycodelin	PAEP
P09486	SPARC	SPARC
P09529	Inhibin beta B chain	INHBB
P09544	Protein Wnt-2	WNT2
P09603	Processed macrophage colony-stimulating factor 1	CSF1
P09681	Gastric inhibitory polypeptide	GIP
P09683	Secretin	SCT
P09919	Granulocyte colony-stimulating factor	CSF3
P0C091	FRAS1-related extracellular matrix protein 3	FREM3
P0C0L4	C4d-A	C4A
P0C0L5	Complement C4-6 alpha chain	C4B
P0C0P6	Neuropeptide S	NPS
P0C7L1	Serine protease inhibitor Kazal-type 8	SPINK8
P0C862	Complement C1q and tumor necrosis factor-related protein	C1QTNF9
	9A
P0C8F1	Prostate and testis expressed protein 4	PATE4
P0CG01	Gastrokine-3	GKN3P
P0CG36	Cryptic family protein 1B	CFC1B
P0CG37	Cryptic protein	CFC1
P0CJ68	Humanin-like protein 1	MTRNR2L1
P0CJ69	Humanin-like protein 2	MTRNR2L2
P0CJ70	Humanin-like protein 3	MTRNR2L3
P0CJ71	Humanin-like protein 4	MTRNR2L4
P0CJ72	Humanin-like protein 5	MTRNR2L5
P0CJ73	Humanin-like protein 6	MTRNR2L6
P0CJ74	Humanin-like protein 7	MTRNR2L7
P0CJ75	Humanin-like protein 8	MTRNR2L8
P0CJ76	Humanin-like protein 9	MTRNR2L9
P0CJ77	Humanin-like protein 10	MTRNR2L10
P0DJD7	Pepsin A-4	PGA4
P0DJD8	Pepsin A-3	PGA3
P0DJD9	Pepsin A-5	PGA5
P0DJI8	Amyloid protein A	SAA1
P0DJI9	Serum amyloid A-2 protein	SAA2
P10082	Peptide YY(3-36)	PYY
P10092	Calcitonin gene-related peptide 2	CALCB
P10124	Serglycin	SRGN
P10145	MDNCF-a	IL8
P10147	MIP-1-alpha(4-69)	CCL3
P10163	Peptide P-D	PRB4
P10451	Osteopontin	SPP1
P10599	Thioredoxin	TXN
P10600	Transforming growth factor beta-3	TGFB3
P10643	Complement component C7	C7
P10645	Vasostatin-2	CHGA
P10646	Tissue factor pathway inhibitor	TFPI
P10720	Platelet factor 4 variant(4-74)	PF4V1
P10745	Retinol-binding protein 3	RBP3
P10767	Fibroblast growth factor 6	FGF6
P10909	Clusterin alpha chain	CLU
P10912	Growth hormone receptor	GHR
P10915	Hyaluronan and proteoglycan link protein 1	HAPLN1
P10966	T-cell surface glycoprotein CD8 beta chain	CD8B
P10997	Islet amyloid polypeptide	IAPP
P11047	Laminin subunit gamma-1	LAMC1
P11150	Hepatic triacylglycerol lipase	LIPC
P11226	Mannose-binding protein C	MBL2
P11464	Pregnancy-specific beta-1-glycoprotein 1	PSG1
P11465	Pregnancy-specific beta-1-glycoprotein 2	PSG2
P11487	Fibroblast growth factor 3	FGF3
P11597	Cholesteryl ester transfer protein	CETP
P11684	Uteroglobin	SCGB1A1
P11686	Pulmonary surfactant-associated protein C	SFTPC
P12034	Fibroblast growth factor 5	FGF5
P12107	Collagen alpha-1(XI) chain	COL11A1
P12109	Collagen alpha-1(VI) chain	COL6A1
P12110	Collagen alpha-2(VI) chain	COL6A2
P12111	Collagen alpha-3(VI) chain	COL6A3
P12259	Coagulation factor V	F5
P12272	PTHrP[1-36]	PTHLH
P12273	Prolactin-inducible protein	PIP
P12544	Granzyme A	GZMA
P12643	Bone morphogenetic protein 2	BMP2
P12644	Bone morphogenetic protein 4	BMP4
P12645	Bone morphogenetic protein 3	BMP3
P12724	Eosinophil cationic protein	RNASE3
P12821	Angiotensin-converting enzyme, soluble form	ACE
P12838	Neutrophil defensin 4	DEFA4
P12872	Motilin	MLN
P13232	Interleukin-7	IL7
P13236	C—C motif chemokine 4	CCL4
P13284	Gamma-interferon-inducible lysosomal thiol reductase	IFI30
P13500	C—C motif chemokine 2	CCL2
P13501	C—C motif chemokine 5	CCL5
P13521	Secretogranin-2	SCG2
P13591	Neural cell adhesion molecule 1	NCAM1
P13611	Versican core protein	VCAN
P13671	Complement component C6	C6
P13688	Carcinoembryonic antigen-related cell adhesion molecule 1	CEACAM1
P13725	Oncostatin-M	OSM
P13726	Tissue factor	F3
P13727	Eosinophil granule major basic protein	PRG2
P13942	Collagen alpha-2(XI) chain	COL11A2
P13987	CD59 glycoprotein	CD59
P14138	Endothelin-3	EDN3
P14174	Macrophage migration inhibitory factor	MIF
P14207	Folate receptor beta	FOLR2
P14222	Perforin-1	PRF1
P14543	Nidogen-1	NID1
P14555	Phospholipase A2, membrane associated	PLA2G2A
P14625	Endoplasmin	HSP90B1
P14735	Insulin-degrading enzyme	IDE
P14778	Interleukin-1 receptor type 1, soluble form	IDE
P14780	82 kDa matrix metalloproteinase-9	MMP9
P15018	Leukemia inhibitory factor	LIF
P15085	Carboxypeptidase Al	CPA1
P15086	Carboxypeptidase B	CPB1
P15151	Poliovirus receptor	PVR
P15169	Carboxypeptidase N catalytic chain	CPN1
P15248	Interleukin-9	IL9
P15291	N-acetyllactosamine synthase	B4GALT1
P15309	PAPf39	ACPP
P15328	Folate receptor alpha	FOLR1
P15374	Ubiquitin carboxyl-terminal hydrolase isozyme L3	UCHL3
P15502	Elastin	ELN
P15509	Granulocyte-macrophage colony-stimulating factor receptor	CSF2RA
	subunit alpha
P15515	Histatin-1	HTN1
P15516	His3-(31-51)-peptide	HTN3
P15692	Vascular endothelial growth factor A	VEGFA
P15814	Immunoglobulin lambda-like polypeptide 1	IGLL1
P15907	Beta-galactoside alpha-2,6-sialyltransferase 1	ST6GAL1
P15941	Mucin-1 subunit beta	MUC1
P16035	Metalloproteinase inhibitor 2	TIMP2
P16112	Aggrecan core protein 2	ACAN
P16233	Pancreatic triacylglycerol lipase	PNLIP
P16442	Histo-blood group ABO system transferase	ABO
P16471	Prolactin receptor	PRLR
P16562	Cysteine-rich secretory protein 2	CRISP2
P16619	C—C motif chemokine 3-like 1	CCL3L1
P16860	BNP(3-29)	NPPB
P16870	Carboxypeptidase E	CPE
P16871	Interleukin-7 receptor subunit alpha	IL7R
P17213	Bactericidal permeability-increasing protein	BPI
P17538	Chymotrypsinogen B	CTRB1
P17931	Galectin-3	LGALS3
P17936	Insulin-like growth factor-binding protein 3	IGFBP3
P17948	Vascular endothelial growth factor receptor 1	FLT1
P18065	Insulin-like growth factor-binding protein 2	IGFBP2
P18075	Bone morphogenetic protein 7	BMP7
P18428	Lipopolysaccharide-binding protein	LBP
P18509	PACAP-related peptide	ADCYAP1
P18510	Interleukin-1 receptor antagonist protein	URN
P18827	Syndecan-1	SDC1
P19021	Peptidylglycine alpha-hydroxylating monooxygenase	PAM
P19235	Erythropoietin receptor	EPOR
P19438	Tumor necrosis factor-binding protein 1	TNFRSF1A
P19652	Alpha-1-acid glycoprotein 2	ORM2
P19801	Amiloride-sensitive amine oxidase [copper-containing]	ABP1
P19823	Inter-alpha-trypsin inhibitor heavy chain H2	ITIH2
P19827	Inter-alpha-trypsin inhibitor heavy chain H1	ITIH1
P19835	Bile salt-activated lipase	CEL
P19875	C—X—C motif chemokine 2	CXCL2
P19876	C—X—C motif chemokine 3	CXCL3
P19883	Follistatin	FST
P19957	Elafin	PI3
P19961	Alpha-amylase 2B	AMY2B
P20061	Transcobalamin-1	TCN1
P20062	Transcobalamin-2	TCN2
P20142	Gastricsin	PGC
P20155	Serine protease inhibitor Kazal-type 2	SPINK2
P20231	Tryptase beta-2	TPSB2
P20333	Tumor necrosis factor receptor superfamily member 1B	TNFRSF1B
P20366	Substance P	TAC1
P20382	Melanin-concentrating hormone	PMCH
P20396	Thyroliberin	TRH
P20742	Pregnancy zone protein	PZP
P20774	Mimecan	OGN
P20783	Neurotrophin-3	NTF3
P20800	Endothelin-2	EDN2
P20809	Interleukin-11	IL11
P20827	Ephrin-A1	EFNA1
P20849	Collagen alpha-1(IX) chain	COL9A1
P20851	C4b-binding protein beta chain	C4BPB
P20908	Collagen alpha-1(V) chain	COL5A1
P21128	Poly(U)-specific endoribonuclease	ENDOU
P21246	Pleiotrophin	PTN
P21583	Kit ligand	KITLG
P21741	Midkine	MDK
P21754	Zona pellucida sperm-binding protein 3	ZP3
P21781	Fibroblast growth factor 7	FGF7
P21802	Fibroblast growth factor receptor 2	FGFR2
P21810	Biglycan	BGN
P21815	Bone sialoprotein 2	IBSP
P21860	Receptor tyrosine-protein kinase erbB-3	ERBB3
P21941	Cartilage matrix protein	MATN1
P22003	Bone morphogenetic protein 5	BMP5
P22004	Bone morphogenetic protein 6	BMP6
P22079	Lactoperoxidase	LPO
P22105	Tenascin-X	TNXB
P22301	Interleukin-10	IL10
P22303	Acetylcholinesterase	ACHE
P22352	Glutathione peroxidase 3	GPX3
P22362	C—C motif chemokine 1	CCL1
P22455	Fibroblast growth factor receptor 4	FGFR4
P22466	Galanin message-associated peptide	GAL
P22692	Insulin-like growth factor-binding protein 4	IGFBP4
P22749	Granulysin	GNLY
P22792	Carboxypeptidase N subunit 2	CPN2
P22891	Vitamin K-dependent protein Z	PROZ
P22894	Neutrophil collagenase	MMP8
P23142	Fibulin-1	FBLN1
P23280	Carbonic anhydrase 6	CA6
P23352	Anosmin-1	KAL1
P23435	Cerebellin-1	CBLN1
P23560	Brain-derived neurotrophic factor	BDNF
P23582	C-type natriuretic peptide	NPPC
P23946	Chymase	CMA1
P24043	Laminin subunit alpha-2	LAMA2
P24071	Immunoglobulin alpha Fc receptor	FCAR
P24347	Stromelysin-3	MMP11
P24387	Corticotropin-releasing factor-binding protein	CRHBP
P24592	Insulin-like growth factor-binding protein 6	IGFBP6
P24593	Insulin-like growth factor-binding protein 5	IGFBP5
P24821	Tenascin	TNC
P24855	Deoxyribonuclease-1	DNASE1
P25067	Collagen alpha-2(VIII) chain	COL8A2
P25311	Zinc-alpha-2-glycoprotein	AZGP1
P25391	Laminin subunit alpha-1	LAMA1
P25445	Tumor necrosis factor receptor superfamily member 6	FAS
P25940	Collagen alpha-3(V) chain	COL5A3
P25942	Tumor necrosis factor receptor superfamily member 5	CD40
P26022	Pentraxin-related protein PTX3	PTX3
P26927	Hepatocyte growth factor-like protein beta chain	MST1
P27169	Serum paraoxonase/arylesterase 1	PON1
P27352	Gastric intrinsic factor	GIF
P27487	Dipeptidyl peptidase 4 membrane form	DPP4
P27539	Embryonic growth/differentiation factor 1	GDF1
P27658	Vastatin	COL8A1
P27797	Calreticulin	CALR
P27918	Properdin	CFP
P28039	Acyloxyacyl hydrolase	AOAH
P28300	Protein-lysine 6-oxidase	LOX
P28325	Cystatin-D	CST5
P28799	Granulin-1	GRN
P29122	Proprotein convertase subtilisin/kexin type 6	PCSK6
P29279	Connective tissue growth factor	CTGF
P29320	Ephrin type-A receptor 3	EPHA3
P29400	Collagen alpha-5(IV) chain	COL4A5
P29459	Interleukin-12 subunit alpha	IL12A
P29460	Interleukin-12 subunit beta	IL12B
P29508	Serpin B3	SERPINB3
P29622	Kallistatin	SERPINA4
P29965	CD40 ligand, soluble form	CD4OLG
P30990	Neurotensin/neuromedin	NNTS
P31025	Lipocalin-1	LCN1
P31151	Protein 5100-A7	S100A7
P31371	Fibroblast growth factor 9	FGF9
P31431	Syndecan-4	SDC4
P31947	14-3-3 protein sigma	SEN
P32455	Interferon-induced guanylate-binding protein 1	GBP1
P32881	Interferon alpha-8	IFNA8
P34096	Ribonuclease 4	RNASE4
P34130	Neurotrophin-4	NTF4
P34820	Bone morphogenetic protein 8B	BMP8B
P35030	Trypsin-3	PRSS3
P35052	Secreted glypican-1	GPC1
P35070	Betacellulin	BTC
P35225	Interleukin-13	IL13
P35247	Pulmonary surfactant-associated protein D	SFTPD
P35318	ADM	ADM
P35542	Serum amyloid A-4 protein	SAA4
P35555	Fibrillin-1	FBN1
P35556	Fibrillin-2	FBN2
P35625	Metalloproteinase inhibitor 3	TIMP3
P35858	Insulin-like growth factor-binding protein complex acid labile	IGFALS
	subunit
P35916	Vascular endothelial growth factor receptor 3	FLT4
P35968	Vascular endothelial growth factor receptor 2	KDR
P36222	Chitinase-3-like protein 1	CHI3L1
P36952	Serpin B5	SERPINB5
P36955	Pigment epithelium-derived factor	SERPINF1
P36980	Complement factor H-related protein 2	CFHR2
P39059	Collagen alpha-1(XV) chain	COL15A1
P39060	Collagen alpha-1(XVIII) chain	C0L18A1
P39877	Calcium-dependent phospholipase A2	PLA2G5
P39900	Macrophage metalloelastase	MMP12
P39905	Glial cell line-derived neurotrophic factor	GDNF
P40225	Thrombopoietin	THPO
P40967	M-alpha	PMEL
P41159	Leptin	LEP
P41221	Protein Wnt-5a	WNT5A
P41222	Prostaglandin-H2 D-isomerase	PTGDS
P41271	Neuroblastoma suppressor of tumorigenicity 1	NBL1
P41439	Folate receptor gamma	FOLR3
P42127	Agouti-signaling protein	ASIP
P42702	Leukemia inhibitory factor receptor	LIFR
P42830	ENA-78(9-78)	CXCL5
P43026	Growth/differentiation factor 5	GDF5
P43251	Biotinidase	BTD
P43652	Afamin	AFM
P45452	Collagenase 3	MMP13
P47710	Casoxin-D	CSN1S1
P47929	Galectin-7	LGALS7B
P47972	Neuronal pentraxin-2	NPTX2
P47989	Xanthine oxidase	XDH
P47992	Lymphotactin	XCL1
P48023	Tumor necrosis factor ligand superfamily member 6,	FASLG
	membrane form
P48052	Carboxypeptidase A2	CPA2
P48061	Stromal cell-derived factor 1	CXCL12
P48304	Lithostathine-1-beta	REG1B
P48307	Tissue factor pathway inhibitor 2	TFPI2
P48357	Leptin receptor	LEPR
P48594	Serpin B4	SERPINB4
P48645	Neuromedin-U-25	NMU
P48740	Mannan-binding lectin serine protease 1	MASP1
P48745	Protein NOV homolog	NOV
P48960	CD97 antigen subunit beta	CD97
P49223	Kunitz-type protease inhibitor 3	SPINT3
P49747	Cartilage oligomeric matrix protein	COMP
P49763	Placenta growth factor	PGF
P49765	Vascular endothelial growth factor B	VEGFB
P49767	Vascular endothelial growth factor C	VEGFC
P49771	Ems-related tyrosine kinase 3 ligand	FLT3LG
P49862	Kallikrein-7	KLK7
P49863	Granzyme K	GZMK
P49908	Selenoprotein P	SEPP1
P49913	Antibacterial protein FALL-39	CAMP
P50607	Tubby protein homolog	TUB
P51124	Granzyme M	GZMM
P51512	Matrix metalloproteinase-16	MMP16
P51654	Glypican-3	GPC3
P51671	Eotaxin	CCL11
P51884	Lumican	LUM
P51888	Prolargin	PRELP
P52798	Ephrin-A4	EFNA4
P52823	Stanniocalcin-1	STC1
P53420	Collagen alpha-4(IV) chain	COL4A4
P53621	Coatomer subunit alpha	COPA
P54108	Cysteine-rich secretory protein 3	CRISP3
P54315	Pancreatic lipase-related protein 1	PNLIPRP1
P54317	Pancreatic lipase-related protein 2	PNLIPRP2
P54793	Arylsulfatase F	ARSE
P55000	Secreted Ly-6/uPAR-related protein 1	SLURP1
P55001	Microfibrillar-associated protein 2	MFAP2
P55056	Apolipoprotein C-IV	APOC4
P55058	Phospholipid transfer protein	PLTP
P55075	Fibroblast growth factor 8	FGF8
P55081	Microfibrillar-associated protein 1	MFAP1
P55083	Microfibril-associated glycoprotein 4	MFAP4
P55107	Bone morphogenetic protein 3B	GDF10
P55145	Mesencephalic astrocyte-derived neurotrophic factor	MANE
P55259	Pancreatic secretory granule membrane major glycoprotein	GP2
	GP2
P55268	Laminin subunit beta-2	LAMB2
P55773	CCL23(30-99)	CCL23
P55774	C—C motif chemokine 18	CCL18
P55789	FAD-linked sulfhydryl oxidase ALR	GFER
P56703	Proto-oncogene Wnt-3	WNT3
P56704	Protein Wnt-3a	WNT3A
P56705	Protein Wnt-4	WNT4
P56706	Protein Wnt-7b	WNT7B
P56730	Neurotrypsin	PRSS12
P56851	Epididymal secretory protein E3-beta	EDDM3B
P56975	Neuregulin-3	NRG3
P58062	Serine protease inhibitor Kazal-type 7	SPINK7
P58215	Lysyl oxidase homolog 3	LOXL3
P58294	Prokineticin-1	PROK1
P58335	Anthrax toxin receptor 2	ANTXR2
P58397	A disintegrin and metalloproteinase with thrombospondin	ADAMTS12
	motifs 12
P58417	Neurexophilin-1	NXPH1
P58499	Protein FAM3B	FAM3B
P59510	A disintegrin and metalloproteinase with thrombospondin	ADAMTS20
	motifs 20
P59665	Neutrophil defensin 1	DEFA1B
P59666	Neutrophil defensin 3	DEFA3
P59796	Glutathione peroxidase 6	GPX6
P59826	BPI fold-containing family B member 3	BPIFB3
P59827	BPI fold-containing family B member 4	BPIFB4
P59861	Beta-defensin 131	DEFB131
P60022	Beta-defensin 1	DEFB1
P60153	Inactive ribonuclease-like protein 9	RNASE9
P60827	Complement C1q tumor necrosis factor-related protein 8	C1QTNF8
P60852	Zona pellucida sperm-binding protein 1	ZP1
P60985	Keratinocyte differentiation-associated protein	KRTDAP
P61109	Kidney androgen-regulated protein	KAP
P61278	Somatostatin-14	SST
P61366	Osteocrin	OSTN
P61626	Lysozyme C	LYZ
P61769	Beta-2-microglobulin	B2M
P61812	Transforming growth factor beta-2	TGFB2
P61916	Epididymal secretory protein El	NPC2
P62502	Epididymal-specific lipocalin-6	LCN6
P62937	Peptidyl-prolyl cis-trans isomerase A	PPIA
P67809	Nuclease-sensitive element-binding protein 1	YBX1
P67812	Signal peptidase complex catalytic subunit SEC11A	SEC11A
P78310	Coxsackievirus and adenovirus receptor	CXADR
P78333	Secreted glypican-5	GPC5
P78380	Oxidized low-density lipoprotein receptor 1	OLR1
P78423	Processed fractalkine	CX3CL1
P78509	Reelin	RELN
P78556	CCL20(2-70)	CCL20
P80075	MCP-2(6-76)	CCL8
P80098	C—C motif chemokine 7	CCL7
P80108	Phosphatidylinositol-glycan-specific phospholipase D	GPLD1
P80162	C—X—C motif chemokine 6	CXCL6
P80188	Neutrophil gelatinase-associated lipocalin	LCN2
P80303	Nucleobindin-2	NUCB2
P80511	Calcitermin	S100A12
P81172	Hepcidin-25	HAMP
P81277	Prolactin-releasing peptide	PRLH
P81534	Beta-defensin 103	DEFB103A
P81605	Dermcidin	DCD
P82279	Protein crumbs homolog 1	CRB1
P82987	ADAMTS-like protein 3	ADAMTSL3
P83105	Serine protease HTRA4	HTRA4
P83110	Serine protease HTRA3	HTRA3
P83859	Orexigenic neuropeptide QRFP	QRFP
P98088	Mucin-SAC	MUC5AC
P98095	Fibulin-2	FBLN2
P98160	Basement membrane-specific heparan sulfate proteoglycan	HSPG2
	core protein
P98173	Protein FAM3A	FAM3A
Q00604	Norrin	NDP
Q00796	Sorbitol dehydrogenase	SORD
Q00887	Pregnancy-specific beta-1-glycoprotein 9	PSG9
Q00888	Pregnancy-specific beta-1-glycoprotein 4	PSG4
Q00889	Pregnancy-specific beta-1-glycoprotein 6	PSG6
Q01523	HD5(56-94)	DEFA5
Q01524	Defensin-6	DEFA6
Q01955	Collagen alpha-3(IV) chain	COL4A3
Q02297	Pro-neuregulin-1, membrane-bound isoform	NRG1
Q02325	Plasminogen-like protein B	PLGLB1
Q02383	Semenogelin-2	SEMG2
Q02388	Collagen alpha-1(VII) chain	COL7A1
Q02505	Mucin-3A	MUC3A
Q02509	Otoconin-90	OC90
Q02747	Guanylin	GUCA2A
Q02763	Angiopoietin-1 receptor	TEK
Q02817	Mucin-2	MUC2
Q02985	Complement factor H-related protein 3	CFHR3
Q03167	Transforming growth factor beta receptor type 3	TGFBR3
Q03403	Trefoil factor 2	TFF2
Q03405	Urokinase plasminogen activator surface receptor	PLAUR
Q03591	Complement factor H-related protein 1	CFHR1
Q03692	Collagen alpha-1(X) chain	COL10A1
Q04118	Basic salivary proline-rich protein 3	PRB3
Q04756	Hepatocyte growth factor activator short chain	HGFAC
Q04900	Sialomucin core protein 24	CD164
Q05315	Eosinophil lysophospholipase	CLC
Q05707	Collagen alpha-1(XIV) chain	COL14A1
Q05996	Processed zona pellucida sperm-binding protein 2	ZP2
Q06033	Inter-alpha-trypsin inhibitor heavy chain H3	ITIH3
Q06141	Regenerating islet-derived protein 3-alpha	REG3A
Q06828	Fibromodulin	FMOD
Q07092	Collagen alpha-1(XVI) chain	COL16A1
Q07325	C—X—C motif chemokine 9	CXCL9
Q07507	Dermatopontin	DPT
Q075Z2	Binder of sperm protein homolog 1	BSPH1
Q07654	Trefoil factor 3	TFF3
Q07699	Sodium channel subunit beta-1	SCN1B
Q08345	Epithelial discoidin domain-containing receptor 1	DDR1
Q08380	Galectin-3-binding protein	LGALS3BP
Q08397	Lysyl oxidase homolog 1	LOXL1
Q08431	Lactadherin	MFGE8
Q08629	Testican-1	SPOCK1
Q08648	Sperm-associated antigen 11B	SPAG11B
Q08830	Fibrinogen-like protein 1	FGL1
Q10471	Polypeptide N-acetylgalactosaminyltransferase 2	GALNT2
Q10472	Polypeptide N-acetylgalactosaminyltransferase 1	GALNT1
Q11201	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-	ST3GAL1
	sialyltransferase 1
Q11203	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-	ST3GAL3
	sialyltransferase
Q11206	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-	ST3GAL4
	sialyltransferase 4
Q12794	Hyaluronidase-1	HYAL1
Q12805	EGF-containing fibulin-like extracellular matrix protein 1	EFEMP1
Q12836	Zona pellucida sperm-binding protein 4	ZP4
Q12841	Follistatin-related protein 1	FSTL1
Q12904	Aminoacyl tRNA synthase complex-interacting	AIMP1
	multifunctional protein 1
Q13018	Soluble secretory phospholipase A2 receptor	PLA2R1
Q13072	B melanoma antigen 1	BAGE
Q13093	Platelet-activating factor acetylhydrolase	PLA2G7
Q13103	Secreted phosphoprotein 24	SPP2
Q13162	Peroxiredoxin-4	PRDX4
Q13201	Platelet glycoprotein la*	MMRN1
Q13214	Semaphorin-3B	SEMA3B
Q13219	Pappalysin-1	PAPPA
Q13231	Chitotriosidase-1	CHIT1
Q13253	Noggin	NOG
Q13261	Interleukin-15 receptor subunit alpha	IL15RA
Q13275	Semaphorin-3F	SEMA3F
Q13291	Signaling lymphocytic activation molecule	SLAME1
Q13316	Dentin matrix acidic phosphoprotein 1	DMP1
Q13361	Microfibrillar-associated protein 5	MFAP5
Q13410	Butyrophilin subfamily 1 member A1	BTN1A1
Q13421	Mesothelin, cleaved form	MSLN
Q13429	Insulin-like growth factor I	IGF-I
Q13443	Disintegrin and metalloproteinase domain-containing	ADAM9
	protein 9
Q13519	Neuropeptide 1	PNOC
Q13751	Laminin subunit beta-3	LAMB3
Q13753	Laminin subunit gamma-2	LAMC2
Q13790	Apolipoprotein F	APOF
Q13822	Ectonucleotide pyrophosphatase/phosphodiesterase family	ENPP2
	member 2
Q14031	Collagen alpha-6(IV) chain	COL4A6
Q14050	Collagen alpha-3(IX) chain	COL9A3
Q14055	Collagen alpha-2(IX) chain	COL9A2
Q14112	Nidogen-2	NID2
Q14114	Low-density lipoprotein receptor-related protein 8	LRP8
Q14118	Dystroglycan	DAG1
Q14314	Fibroleukin	FGL2
Q14393	Growth arrest-specific protein 6	GAS6
Q14406	Chorionic somatomammotropin hormone-like 1	CSHL1
Q14507	Epididymal secretory protein E3-alpha	EDDM3A
Q14508	WAP four-disulfide core domain protein 2	WFDC2
Q14512	Fibroblast growth factor-binding protein 1	FGFBP1
Q14515	SPARC-like protein 1	SPARCL1
Q14520	Hyaluronan-binding protein 2 27 kDa light chain	HABP2
Q14563	Semaphorin-3A	SEMA3A
Q14623	Indian hedgehog protein	IHH
Q14624	Inter-alpha-trypsin inhibitor heavy chain H4	ITIH4
Q14667	UPF0378 protein KIAA0100	KIAA0100
Q14703	Membrane-bound transcription factor site-1 protease	MBTPS1
Q14766	Latent-transforming growth factor beta-binding protein 1	LTBP1
Q14767	Latent-transforming growth factor beta-binding protein 2	LTBP2
Q14773	Intercellular adhesion molecule 4	ICAM4
Q14993	Collagen alpha-1(XIX) chain	COL19A1
Q14CN2	Calcium-activated chloride channel regulator 4, 110 kDa	CLCA4
	form
Q15046	Lysine--tRNA ligase	KARS
Q15063	Periostin	POSTN
Q15109	Advanced glycosylation end product-specific receptor	AGER
Q15113	Procollagen C-endopeptidase enhancer 1	PCOLCE
Q15166	Serum paraoxonase/lactonase 3	PON3
Q15195	Plasminogen-like protein A	PLGLA
Q15198	Platelet-derived growth factor receptor-like protein	PDGFRL
Q15223	Poliovirus receptor-related protein 1	PVRL1
Q15238	Pregnancy-specific beta-1-glycoprotein 5	PSG5
Q15363	Transmembrane emp24 domain-containing protein 2	TMED2
Q15375	Ephrin type-A receptor 7	EPHA7
Q15389	Angiopoietin-1	ANGPT1
Q15465	Sonic hedgehog protein	SHH
Q15485	Ficolin-2	FCN2
Q15517	Corneodesmosin	CDSN
Q15582	Transforming growth factor-beta-induced protein ig-h3	TGFBI
Q15661	Tryptase alpha/beta-1	TPSAB1
Q15726	Metastin	KISS1
Q15782	Chitinase-3-like protein 2	CHI3L2
Q15828	Cystatin-M	CST6
Q15846	Clusterin-like protein 1	CLUL1
Q15848	Adiponectin	ADIPOQ
Q16206	Protein disulfide-thiol oxidoreductase	ENOX2
Q16270	Insulin-like growth factor-binding protein 7	IGFBP7
Q16363	Laminin subunit alpha-4	LAMA4
Q16378	Proline-rich protein 4	PRR4
Q16557	Pregnancy-specific beta-1-glycoprotein 3	PSG3
Q16568	CART(42-89)	CARTPT
Q16610	Extracellular matrix protein 1	ECM1
Q16619	Cardiotrophin-1	CTF1
Q16623	Syntaxin-1A	STX1A
Q16627	HCC-1(9-74)	CCL14
Q16651	Prostasin light chain	PRSS8
Q16661	Guanylate cyclase C-activating peptide 2	GUCA2B
Q16663	CCL15(29-92)	CCL15
Q16674	Melanoma-derived growth regulatory protein	MIA
Q16769	Glutaminyl-peptide cyclotransferase	QPCT
Q16787	Laminin subunit alpha-3	LAMA3
Q16842	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-	ST3GAL2
	sialyltransferase 2
Q17RR3	Pancreatic lipase-related protein 3	PNLIPRP3
Q17RW2	Collagen alpha-1(XXIV) chain	COL24A1
Q17RY6	Lymphocyte antigen 6K	LY6K
Q1L6U9	Prostate-associated microseminoprotein	MSMP
Q1W4C9	Serine protease inhibitor Kazal-type 13	SPINK13
Q1ZYL8	lzumo sperm-egg fusion protein 4	IZUMO4
Q29960	HLA class I histocompatibility antigen, Cw-16 alpha chain	HLA-C
Q2I0M5	R-spondin-4	RSPO4
Q2L409	Serine protease 53	PRSS53
Q2MKA7	R-spondin-1	RSPO1
Q2MV58	Tectonic-1	TCTN1
Q2TAL6	Brorin	VWC2
Q2UY09	Collagen alpha-1(XXVIII) chain	COL28A1
Q2VPA4	Complement component receptor 1-like protein	CR11
Q2WEN9	Carcinoembryonic antigen-related cell adhesion molecule 16	CEACAM16
Q30KP8	Beta-defensin 136	DEFB136
Q30KP9	Beta-defensin 135	DEFB135
Q30KQ1	Beta-defensin 133	DEFB133
Q30K02	Beta-defensin 130	DEFB130
Q30K04	Beta-defensin 116	DEFB116
Q30K05	Beta-defensin 115	DEFB115
Q30K06	Beta-defensin 114	DEFB114
Q30K07	Beta-defensin 113	DEFB113
Q30K08	Beta-defensin 112	DEFB112
Q30K09	Beta-defensin 110	DEFB110
Q30KR1	Beta-defensin 109	DEFB109P1
Q32P28	Prolyl 3-hydroxylase 1	LEPRE1
Q3B7J2	Glucose-fructose oxidoreductase domain-containing protein 2	GFOD2
Q3SY79	Protein Wnt	WNT3A
Q3T906	N-acetylglucosamine-1-phosphotransferase subunits	GNPTAB
	alpha/beta
Q495T6	Membrane metallo-endopeptidase-like 1	MMEL1
Q49AH0	Cerebral dopamine neurotrophic factor	CDNF
Q4G0G5	Secretoglobin family 2B member 2	SCGB2B2
Q4G0M1	Protein FAM1326	FAM1326
Q4LDE5	Sushi, von Willebrand factor type A, EGF and pentraxin	SVEP1
	domain-containing protein 1
Q40Y38	Beta-defensin 134	DEFB134
Q4VAJ4	Protein Wnt	WNT10B
Q4W5P6	Protein TMEM155	TMEM155
Q4ZHG4	Fibronectin type III domain-containing protein 1	FNDDC1
Q53H76	Phospholipase A1 member A	PLA1A
Q53RD9	Fibulin-7	FBLN7
Q53S33	BoIA-like protein 3	BOLA3
Q5BLP8	Neuropeptide-like protein C4orf48	C4orf48
Q5DT21	Serine protease inhibitor Kazal-type 9	SPINK9
Q5EBL8	PDZ domain-containing protein 11	PDZD11
Q5FYB0	Arylsulfatase J	ARSJ
Q5FY61	Arylsulfatase I	ARSI
Q5GAN3	Ribonuclease-like protein 13	RNASE13
Q5GAN4	Ribonuclease-like protein 12	RNASE12
Q5GAN6	Ribonuclease-like protein 10	RNASE10
Q5GFL6	von Willebrand factor A domain-containing protein 2	VWA2
Q5H8A3	Neuromedin-S	NMS
Q5H8C1	FRAS1-related extracellular matrix protein 1	FREM1
Q5IJ48	Protein crumbs homolog 2	CRB2
Q5J5C9	Beta-defensin 121	DEFB121
Q5JS37	NHL repeat-containing protein 3	NHLRC3
Q5JTB6	Placenta-specific protein 9	PLAC9
Q5JU69	Torsin-2A	TOR2A
Q5JXM2	Methyltransferase-like protein 24	METTL24
Q5JZY3	Ephrin type-A receptor 10	EPHA10
Q5K4E3	Polyserase-2	PRSS36
Q5SRR4	Lymphocyte antigen 6 complex locus protein G5c	LY6G5C
Q5T1H1	Protein eyes shut homolog	EYS
Q5T4F7	Secreted frizzled-related protein 5	SFRP5
Q5T4W7	Artemin	ARTN
Q5T7M4	Protein FAM132A	FAM132A
Q5TEH8	Protein Wnt	WNT2B
Q5TIE3	von Willebrand factor A domain-containing protein 561	VWA5B1
Q5UCC4	ER membrane protein complex subunit 10	EMC10
Q5V5T6	Abhydrolase domain-containing protein FAM10861	FAM108B1
Q5VTL7	Fibronectin type III domain-containing protein 7	FNDC7
Q5VUM1	UPF0369 protein C6orf57	C6orf57
Q5VV43	Dyslexia-associated protein KIAA0319	KIAA0319
Q5VWW1	Complement C1q-like protein 3	C1QL3
Q5VXI9	Lipase member N	LIPN
Q5VXJ0	Lipase member K	LIPK
Q5VXM1	CUB domain-containing protein 2	CDCP2
Q5VYX0	Renalase	RNLS
Q5VYY2	Lipase member M	LIPM
Q5W186	Cystatin-9	CST9
Q5W5W9	Regulated endocrine-specific protein 18	RE5P18
Q5XG92	Carboxylesterase 4A	CES4A
Q63H02	Pikachurin	EGFLAM
Q64103	Meteorin-like protein	METRNL
Q66K79	Carboxypeptidase Z	CPZ
Q685J3	Mucin-17	MUC17
Q68BL7	Olfactomedin-like protein 2A	OLFML2A
Q68BL8	Olfactomedin-like protein 2B	OLFML2B
Q68DV7	E3 ubiquitin-protein ligase RNF43	RNF43
Q6B9Z1	Insulin growth factor-like family member 4	IGFL4
Q6BAA4	Fc receptor-like B	FCRLB
Q6E0U4	Dermokine	DMKN
Q6EMK4	Vasorin	VASN
Q6FHJ7	Secreted frizzled-related protein 4	SFRP4
Q6GPI1	Chymotrypsin B2 chain B	CTRB2
Q6GT58	Probable carboxypeptidase PM20D1	PM20D1
Q6H9L7	Isthmin-2	ISM2
Q61E36	Ovostatin homolog 2	OVOS2
Q61E37	Ovostatin homolog 1	OVOS1
Q61E38	Serine protease inhibitor Kazal-type 14	SPINK14
Q6ISS4	Leukocyte-associated immunoglobulin-like receptor 2	LAIR2
Q6JVE5	Epididymal-specific lipocalin-12	LCN12
Q6JVE6	Epididymal-specific lipocalin-10	LCN10
Q6JVE9	Epididymal-specific lipocalin-8	LCN8
Q6KF10	Growth/differentiation factor 6	GDF6
Q6MZW2	Follistatin-related protein 4	FSTL4
Q6N5X1	Coiled-coil domain-containing protein 70	CCDC70
Q6NT32	Carboxylesterase 5A	CES5A
Q6NT52	Choriogonadotropin subunit beta variant 2	CGB2
Q6NUI6	Chondroadherin-like protein	CHADL
Q6NUJ1	Saposin A-like	PSAPL1
Q6P093	Arylacetamide deacetylase-like 2	AADACL2
Q6P4A8	Phospholipase B-like 1	PLBD1
Q6P552	UPF0762 protein C6orf58	C6orf58
Q6P988	Protein notum homolog	NOTUM
Q6PCB0	von Willebrand factor A domain-containing protein 1	VWA1
Q6PDA7	Sperm-associated antigen 11A	SPAG11A
Q6PEWO	Inactive serine protease 54	PRSS54
Q6PEZ8	Podocan-like protein 1	PODNL1
Q6PKH6	Dehydrogenase/reductase SDR family member 4-like 2	DHRS4L2
Q60788	Apolipoprotein A-V	APOA5
Q6SPF0	Atherin	SAMD1
Q6UDR6	Kunitz-type protease inhibitor 4	SPINT4
Q6URK8	Testis, prostate and placenta-expressed protein	TEPP
Q6UW01	Cerebellin-3	CBLN3
Q6UW10	Surfactant-associated protein 2	SFTA2
Q6UW15	Regenerating islet-derived protein 3-gamma	REG3G
Q6UW32	Insulin growth factor-like family member 1	IGFL1
Q6UW78	UPF0723 protein C11orf83	C11orf83
Q6UW88	Epigen	EPGN
Q6UWE3	Colipase-like protein 2	CLPSL2
Q6UWF7	NXPE family member 4	NXPE4
Q6UWF9	Protein FAM180A	FAM180A
Q6UWM5	GLIPR1-like protein 1	GLIPR1L1
Q6UWN8	Serine protease inhibitor Kazal-type 6	SPINK6
Q6UWP2	Dehydrogenase/reductase SDR family member 11	DHRS11
Q6UWP8	Suprabasin	SBSN
Q6UW05	Lysozyme-like protein 1	LYZL1
Q6UW07	Insulin growth factor-like family member 2	IGFL2
Q6UWR7	Ectonucleotide pyrophosphatase/phosphodiesterase family	ENPP6
	member 6 soluble form
Q6UWT2	Adropin	ENHO
Q6UWU2	Beta-galactosidase-1-like protein	GLB1L
Q6UWW0	Lipocalin-15	LCN15
Q6UWX4	HHIP-like protein 2	HHIPL2
Q6UWY0	Arylsulfatase K	ARSK
Q6UWY2	Serine protease 57	PRSS57
Q6UWY5	Olfactomedin-like protein 1	OLFML1
Q6UX06	Olfactomedin-4	OLFM4
Q6UX07	Dehydrogenase/reductase SDR family member 13	DHRS13
Q6UX39	Amelotin	AMTN
Q6UX46	Protein FAM1506	FAM1506
Q6UX73	UPF0764 protein C16orf89	C16orf89
Q6UXBO	Protein FAM131A	FAM131A
Q6UX61	Insulin growth factor-like family member 3	IGFL3
Q6UX62	VEGF co-regulated chemokine 1	CXCL17
Q6UXF7	C-type lectin domain family 18 member B	CLEC18I3
Q6UXHO	Hepatocellular carcinoma-associated protein TD26	C19orf80
Q6UXH1	Cysteine-rich with EGF-like domain protein 2	CRELD2
Q6UXH8	Collagen and calcium-binding EGF domain-containing protein 1	CCBE1
Q6UXH9	Inactive serine protease PAMR1	PAMR1
Q6UXI7	Vitrin	VIT
Q6UXI9	Nephronectin	NPNT
Q6UXN2	Trem-like transcript 4 protein	TREML4
Q6UXSO	C-type lectin domain family 19 member A	CLEC19A
Q6UXT8	Protein FAM150A	FAM150A
Q6UXT9	Abhydrolase domain-containing protein 15	ABHD15
Q6UXV4	Apolipoprotein O-like	APOOL
Q6UXX5	Inter-alpha-trypsin inhibitor heavy chain H6	ITIH6
Q6UXX9	R-spondin-2	RSPO2
Q6UY14	ADAMTS-like protein 4	ADAMTSL4
Q6UY27	Prostate and testis expressed protein 2	PATE2
Q6W4X9	Mucin-6	MUC6
Q6WN34	Chordin-like protein 2	CHRDL2
Q6WRI0	Immunoglobulin superfamily member 10	IGSF10
Q6X4U4	Sclerostin domain-containing protein 1	SOSTDC1
Q6X784	Zona pellucida-binding protein 2	ZPBP2
Q6XE38	Secretoglobin family 1D member 4	SCGB1D4
Q6XPR3	Repetin	RPTN
Q6XZBO	Lipase member I	LIPI
Q6ZMM2	ADAMTS-like protein 5	ADAMTSL5
Q6ZMPO	Thrombospondin type-1 domain-containing protein 4	THSD4
Q6ZNFO	Iron/zinc purple acid phosphatase-like protein	PAPL
Q6ZRIO	Otogelin	OTOG
Q6ZRP7	Sulfhydryl oxidase 2	QSOX2
Q6ZWJ8	Kielin/chordin-like protein	KCP
Q75N90	Fibrillin-3	FBN3
Q76510	Urotensin-2B	UTS2D
Q76658	Protein FAM5C	FAM5C
Q76LX8	A disintegrin and metalloproteinase with thrombospondin	ADAMTS13
	motifs 13
Q76M96	Coiled-coil domain-containing protein 80	CCDC80
Q7L1S5	Carbohydrate sulfotransferase 9	CHST9
Q7L513	Fc receptor-like A	FCRLA
Q7L8A9	Vasohibin-1	VASH1
Q7RTM1	Otopetrin-1	OTOP1
Q7RTW8	Otoancorin	OTOA
Q7RTY5	Serine protease 48	PRSS48
Q7RTY7	Ovochymase-1	OVCH1
Q7RTZ1	Ovochymase-2	OVCH2
Q7Z304	MAM domain-containing protein 2	MAMDC2
Q7Z3S9	Notch homolog 2 N-terminal-like protein	NOTCH2NL
Q7Z4H4	Intermedin-short	ADM2
Q7Z4P5	Growth/differentiation factor 7	GDF7
Q7Z4R8	UPF0669 protein C6orf120	C6orf120
Q7Z4W2	Lysozyme-like protein 2	LYZL2
Q7Z5A4	Serine protease 42	PRSS42
Q7Z5A7	Protein FAM19A5	FAM19A5
Q7Z5A8	Protein FAM19A3	FAM19A3
Q7Z5A9	Protein FAM19A1	FAM19A1
Q7Z5J1	Hydroxysteroid 11-beta-dehydrogenase 1-like protein	HSD11B1L
Q7Z5L0	Vitelline membrane outer layer protein 1 homolog	VMO1
Q7Z5L3	Complement Clq-like protein 2	C1QL2
Q7Z5L7	Podocan	PODN
Q7Z5P4	17-beta-hydroxysteroid dehydrogenase 13	HSD17B13
Q7Z5P9	Mucin-19	MUC19
Q7Z5Y6	Bone morphogenetic protein 8A	BMP8A
Q7Z7B7	Beta-defensin 132	DEFB132
Q7Z7B8	Beta-defensin 128	DEFB128
Q7Z7C8	Transcription initiation factor TFIID subunit 8	TAF8
Q7Z7H5	Transmembrane emp24 domain-containing protein 4	TMED4
Q865G7	Lysozyme g-like protein 2	LYG2
Q86519	Protein CEI	C5orf38
Q86TE4	Leucine zipper protein 2	LUZP2
Q86TH1	ADAMTS-like protein 2	ADAMTSL2
Q86U17	Serpin A11	SERPINA11
Q86UU9	Endokinin-A	TAC4
Q86UW8	Hyaluronan and proteoglycan link protein 4	HAPLN4
Q86UX2	Inter-alpha-trypsin inhibitor heavy chain H5	ITIH5
Q86V24	Adiponectin receptor protein 2	ADIPOR2
Q86VB7	Soluble CD163	CD163
Q86VR8	Four-jointed box protein 1	FJX1
Q86WD7	Serpin A9	SERPINA9
Q86WN2	Interferon epsilon	IFNE
Q86W53	Placenta-specific 1-like protein	PLAC1L
Q86X52	Chondroitin sulfate synthase 1	CHSY1
Q86XP6	Gastrokine-2	GKN2
Q86X55	Angiopoietin-related protein 5	ANGPTL5
Q86Y27	B melanoma antigen 5	BAGE5
Q86Y28	B melanoma antigen 4	BAGE4
Q86Y29	B melanoma antigen 3	BAGE3
Q86Y30	B melanoma antigen 2	BAGE2
Q86Y38	Xylosyltransferase 1	XYLT1
Q86Y78	Ly6/PLAUR domain-containing protein 6	LYPD6
Q86YD3	Transmembrane protein 25	TMEM25
Q86YJ6	Threonine synthase-like 2	THNSL2
Q86YW7	Glycoprotein hormone beta-5	GPHB5
Q86Z23	Complement Clq-like protein 4	C1QL4
Q8IU57	Interleukin-28 receptor subunit alpha	IL28RA
Q8IUA0	WAP four-disulfide core domain protein 8	WFDC8
Q8IUB2	WAP four-disulfide core domain protein 3	WFDC3
Q8IUB3	Protein WFDC106	WFDC10B
Q8IUB5	WAP four-disulfide core domain protein 13	WFDC13
Q8IUH2	Protein CREG2	CREG2
Q8IUK5	Plexin domain-containing protein 1	PLXDC1
Q8IUL8	Cartilage intermediate layer protein 2 C2	CILP2
Q8IUX7	Adipocyte enhancer-binding protein 1	AEBP1
Q8IUX8	Epidermal growth factor-like protein 6	EGFL6
Q8IVL8	Carboxypeptidase O	CPO
Q8IVN8	Somatomedin-B and thrombospondin type-1 domain-	SBSPON
	containing protein
Q8IVW8	Protein spinster homolog 2	SPNS2
Q8IW75	Serpin A12	SERPINA12
Q8IW92	Beta-galactosidase-1-like protein 2	GLB1L2
Q8IWL1	Pulmonary surfactant-associated protein A2	SFTPA2
Q8IWL2	Pulmonary surfactant-associated protein A1	SFTPA1
Q8IWV2	Contactin-4	CNTN4
Q8IWY4	Signal peptide, CUB and EGF-like domain-containing protein 1	SCUBE1
Q8IX30	Signal peptide, CUB and EGF-like domain-containing protein 3	SCUBE3
Q8IXA5	Sperm acrosome membrane-associated protein 3,	SPACA3
	membrane form
Q81X131	DnaJ homolog subfamily C member 10	DNAJC10
Q8IXL6	Extracellular serine/threonine protein kinase Fam20C	FAM20C
Q8IYD9	Lung adenoma susceptibility protein 2	LAS2
Q8IYP2	Serine protease 58	PR5558
Q8IY55	Osteoclast-associated immunoglobulin-like receptor	OSCAR
Q8IZC6	Collagen alpha-1(XXVII) chain	COL27A1
Q8IZJ3	C3 and PZP-like alpha-2-macroglobulin domain-containing	CPAMD8
	protein 8
Q8IZN7	Beta-defensin 107	DEFB107B
Q8N0V4	Leucine-rich repeat LGI family member 2	LGI2
Q8N104	Beta-defensin 106	DEFB106B
Q8N119	Matrix metalloproteinase-21	MMP21
Q8N129	Protein canopy homolog 4	CNPY4
Q8N135	Leucine-rich repeat LGI family member 4	LGI4
Q8N145	Leucine-rich repeat LGI family member 3	LGI3
Q8N158	Glypican-2	GPC2
Q8N1E2	Lysozyme g-like protein 1	LYG1
Q8N2E2	von Willebrand factor D and EGF domain-containing protein	VWDE
Q8N2E6	Prosalusin	TOR2A
Q8N2S1	Latent-transforming growth factor beta-binding protein 4	LTBP4
Q8N302	Angiogenic factor with G patch and FHA domains 1	AGGF1
Q8N307	Mucin-20	MUC20
Q8N323	NXPE family member 1	NXPE1
Q8N387	Mucin-15	MUC15
Q8N3Z0	Inactive serine protease 35	PRSS35
Q8N436	Inactive carboxypeptidase-like protein X2	CPXM2
Q8N474	Secreted frizzled-related protein 1	SFRP1
Q8N475	Follistatin-related protein 5	FSTL5
Q8N4F0	BPI fold-containing family B member 2	BPIFB2
Q8N4T0	Carboxypeptidase A6	CPA6
Q8N5W8	Protein FAM246	FAM246
Q8N687	Beta-defensin 125	DEFB125
Q8N688	Beta-defensin 123	DEFB123
Q8N690	Beta-defensin 119	DEFB119
Q8N6C5	Immunoglobulin superfamily member 1	IGSF1
Q8N6C8	Leukocyte immunoglobulin-like receptor subfamily A	LILRA3
	member 3
Q8N6G6	ADAMTS-like protein 1	ADAMTSL1
Q8N6Y2	Leucine-rich repeat-containing protein 17	LRRC17
Q8N729	Neuropeptide W-23	NPW
Q8N8U9	BMP-binding endothelial regulator protein	BMPER
Q8N907	DAN domain family member 5	DAND5
Q8NAT1	Glycosyltransferase-like domain-containing protein 2	GTDC2
Q8NAU1	Fibronectin type III domain-containing protein 5	FNDC5
Q8NB37	Parkinson disease 7 domain-containing protein 1	PDDC1
Q8NBI3	Draxin	DRAXIN
Q8NBM8	Prenylcysteine oxidase-like	PCYOX1L
Q8NBP7	Proprotein convertase subtilisin/kexin type 9	PCSK9
Q8NBQ5	Estradiol 17-beta-dehydrogenase 11	HSD17611
Q8NBV8	Synaptotagmin-8	SYT8
Q8NCC3	Group XV phospholipase A2	PLA2G15
Q8NCF0	C-type lectin domain family 18 member C	CLEC18C
Q8NCW5	NAD(P)H-hydrate epimerase	APOA1BP
Q8NDA2	Hemicentin-2	HMCN2
Q8NDX9	Lymphocyte antigen 6 complex locus protein G5b	LY6G5B
Q8NDZ4	Deleted in autism protein 1	C3orf58
Q8NEB7	Acrosin-binding protein	ACRBP
Q8NES8	Beta-defensin 124	DEFB124
Q8NET1	Beta-defensin 10813	DEFB1086
Q8NEX5	Protein WFDC9	WFDC9
Q8NEX6	Protein WFDC11	WFDC11
Q8NF86	Serine protease 33	PRSS33
Q8NFM7	Interleukin-17 receptor D	IL17RD
Q8NFQ5	BPI fold-containing family B member 6	BPIFB6
Q8NFQ6	BPI fold-containing family C protein	BPIFC
Q8NFU4	Follicular dendritic cell secreted peptide	FDCSP
Q8NFW1	Collagen alpha-1(XXII) chain	COL22A1
Q8NG35	Beta-defensin 105	DEFB1056
Q8NG41	Neuropeptide B-23	NPB
Q8NHW6	Otospiralin	OTOS
Q8NI99	Angiopoietin-related protein 6	ANGPTL6
Q8TAA1	Probable ribonuclease 11	RNASE11
Q8TAG5	V-set and transmembrane domain-containing protein 2A	VSTM2A
Q8TAL6	Fin bud initiation factor homolog	FIBIN
Q8TAT2	Fibroblast growth factor-binding protein 3	FGFBP3
Q8TAX7	Mucin-7	MUC7
Q8TB22	Spermatogenesis-associated protein 20	SPATA20
Q8TB73	Protein NDNF	NDNF
Q8TB96	T-cell immunomodulatory protein	ITFG1
Q8TC92	Protein disulfide-thiol oxidoreductase	ENOX1
Q8TCV5	WAP four-disulfide core domain protein 5	WFDC5
Q8TD06	Anterior gradient protein 3 homolog	AGR3
Q8TD33	Secretoglobin family 1C member 1	SCGB1C1
Q8TD46	Cell surface glycoprotein CD200 receptor 1	CD200R1
Q8TDE3	Ribonuclease 8	RNASE8
Q8TDF5	Neuropilin and tolloid-like protein 1	NETO1
Q8TDL5	BPI fold-containing family B member 1	BPIFB1
Q8TE56	A disintegrin and metalloproteinase with thrombospondin	ADAMTS17
	motifs 17
Q8TE57	A disintegrin and metalloproteinase with thrombospondin	ADAMTS16
	motifs 16
Q8TE58	A disintegrin and metalloproteinase with thrombospondin	ADAMTS15
	motifs 15
Q8TE59	A disintegrin and metalloproteinase with thrombospondin	ADAMTS19
	motifs 19
Q8TE60	A disintegrin and metalloproteinase with thrombospondin	ADAMTS18
	motifs 18
Q8TE99	Acid phosphatase-like protein 2	ACPL2
Q8TER0	Sushi, nidogen and EGF-like domain-containing protein 1	SNED1
Q8TEU8	WAP, kazal, immunoglobulin, kunitz and NTR domain-	WFIKKN2
	containing protein 2
Q8WTQ1	Beta-defensin 104	DEFB1046
Q8WTR8	Netrin-5	NTN5
Q8WTU2	Scavenger receptor cysteine-rich domain-containing group B	SRCRB4D
	protein
Q8WU66	Protein TSPEAR	TSPEAR
Q8WUA8	Tsukushin	TSKU
Q8WUF8	Protein FAM172A	FAM172A
Q8WUJ1	Neuferricin	CYB5D2
Q8WUY1	UPF0670 protein THEM6	THEM6
Q8WVN6	Secreted and transmembrane protein 1	SECTM1
Q8WVQ1	Soluble calcium-activated nucleotidase 1	CANT1
Q8WWAO	Intelectin-1	ITLN1
Q8WWG1	Neuregulin-4	NRG4
Q8WWQ2	Inactive heparanase-2	HPSE2
Q8WWU7	Intelectin-2	ITLN2
Q8WWY7	WAP four-disulfide core domain protein 12	WFDC12
Q8WWY8	Lipase member H	LIPH
Q8WWZ8	Oncoprotein-induced transcript 3 protein	OIT3
Q8WX39	Epididymal-specific lipocalin-9	LCN9
Q8WXA2	Prostate and testis expressed protein 1	PATE1
Q8WXD2	Secretogranin-3	SCG3
Q8WXF3	Relaxin-3 A chain	RLN3
Q8WXI7	Mucin-16	MUC16
Q8WX08	Carboxypeptidase A5	CPA5
Q8WX58	A disintegrin and metalloproteinase with thrombospondin	ADAMTS14
	motifs 14
Q92484	Acid sphingomyelinase-like phosphodiesterase 3a	SMPDL3A
Q92485	Acid sphingomyelinase-like phosphodiesterase 3b	SMPDL3B
Q92496	Complement factor H-related protein 4	CFHR4
Q92520	Protein FAM3C	FAM3C
Q92563	Testican-2	SPOCK2
Q92583	C—C motif chemokine 17	CCL17
Q92626	Peroxidasin homolog	PXDN
Q92743	Serine protease HTRA1	HTRA1
Q92752	Tenascin-R	TNR
Q92765	Secreted frizzled-related protein 3	FRZB
Q92819	Hyaluronan synthase 2	HAS2
Q92820	Gamma-glutamyl hydrolase	GGH
Q92824	Proprotein convertase subtilisin/kexin type 5	PCSK5
Q92832	Protein kinase C-binding protein NELL1	NELL1
Q92838	Ectodysplasin-A, membrane form	EDA
Q92874	Deoxyribonuclease-1-like 2	DNASE1L2
Q92876	Kallikrein-6	KLK6
Q92913	Fibroblast growth factor 13	FGF13
Q92954	Proteoglycan 4 C-terminal part	PRG4
Q93038	Tumor necrosis factor receptor superfamily member 25	TNFRSF25
Q93091	Ribonuclease K6	RNASE6
Q93097	Protein Wnt-2b	WNT2B
Q93098	Protein Wnt-8b	WNT8B
Q95460	Major histocompatibility complex class l-related gene	MR1
	protein
Q969D9	Thymic stromal lymphopoietin	TSLP
Q969E1	Liver-expressed antimicrobial peptide 2	LEAP2
Q969H8	UPF0556 protein C19orf10	C19orf10
Q969Y0	NXPE family member 3	NXPE3
Q96A54	Adiponectin receptor protein 1	ADIPOR1
Q96A83	Collagen alpha-1(XXVI) chain	EMID2
Q96A84	EMI domain-containing protein 1	EMID1
Q96A98	Tuberoinfundibular peptide of 39 residues	PTH2
Q96A99	Pentraxin-4	PTX4
Q96BH3	Epididymal sperm-binding protein 1	ELSPBP1
Q961301	Protein FAM3D	FAM3D
Q96CG8	Collagen triple helix repeat-containing protein 1	CTHRC1
Q96DA0	Zymogen granule protein 16 homolog B	ZG166
Q96DN2	von Willebrand factor C and EGF domain-containing protein	VWCE
Q96DR5	BPI fold-containing family A member 2	BPIFA2
Q96DR8	Mucin-like protein 1	MUCL1
Q96DX4	RING finger and SPRY domain-containing protein 1	RSPRY1
Q96EE4	Coiled-coil domain-containing protein 126	CCDC126
Q96G56	Abhydrolase domain-containing protein FAM108A1	FAM108A1
Q96GW7	Brevican core protein	BCAN
Q96HF1	Secreted frizzled-related protein 2	SFRP2
Q96182	Kazal-type serine protease inhibitor domain-containing	KAZALD1
	protein 1
Q96ID5	Immunoglobulin superfamily member 21	IG5F21
Q96118	Leucine-rich repeat and calponin homology domain-	LRCH3
	containing protein 3
Q96IY4	Carboxypeptidase B2	CPB2
Q96JB6	Lysyl oxidase homolog 4	LOXL4
Q96JK4	HHIP-like protein 1	HHIPL1
Q96KN2	Beta-Ala-His dipeptidase	CNDP1
Q96KW9	Protein SPACA7	SPACA7
Q96KX0	Lysozyme-like protein 4	LYZL4
Q96L15	Ecto-ADP-ribosyltransferase 5	ART5
Q96LB8	Peptidoglycan recognition protein 4	PGLYRP4
Q96LB9	Peptidoglycan recognition protein 3	PGLYRP3
Q96LC7	Sialic acid-binding Ig-like lectin 10	SIGLEC10
Q96LR4	Protein FAM19A4	FAM19A4
Q96MK3	Protein FAM20A	FAM20A
Q96M53	Glycosyltransferase 1 domain-containing protein 1	GLT1D1
Q96NY8	Processed poliovirus receptor-related protein 4	PVRL4
Q96NZ8	WAP, kazal, immunoglobulin, kunitz and NTR domain-	WFIKKN1
	containing protein 1
Q96NZ9	Proline-rich acidic protein 1	PRAP1
Q96P44	Collagen alpha-1(XXI) chain	COL21A1
Q96PB7	Noelin-3	OLFM3
Q96PC5	Melanoma inhibitory activity protein 2	MIA2
Q96PD5	N-acetylmuramoyl-L-alanine amidase	PGLYRP2
Q96PH6	Beta-defensin 118	DEFB118
Q96PL1	Secretoglobin family 3A member 2	SCGB3A2
Q96PL2	Beta-tectorin	TECTB
Q960H8	Sperm acrosome-associated protein 5	SPACA5
Q960R1	Secretoglobin family 3A member 1	SCGB3A1
Q960U1	Protocadherin-15	PCDH15
Q960V1	Hedgehog-interacting protein	HHIP
Q96RW7	Hemicentin-1	HMCN1
Q96S42	Nodal homolog	NODAL
Q96S86	Hyaluronan and proteoglycan link protein 3	HAPLN3
Q96SL4	Glutathione peroxidase 7	GPX7
Q96SM3	Probable carboxypeptidase X1	CPXM1
Q96T91	Glycoprotein hormone alpha-2	GPHA2
Q99062	Granulocyte colony-stimulating factor receptor	CSF3R
Q99102	Mucin-4 alpha chain	MUC4
Q99217	Amelogenin, X isoform	AM+LX
Q99218	Amelogenin, Y isoform	AMELY
Q99435	Protein kinase C-binding protein NELL2	NELL2
Q99470	Stromal cell-derived factor 2	SDF2
Q99542	Matrix metalloproteinase-19	MMP19
Q99574	Neuroserpin	SERPINI1
Q99584	Protein S100-A13	S100A13
Q99616	C—C motif chemokine 13	CCL13
Q99645	Epiphycan	EPYC
Q99674	Cell growth regulator with EF hand domain protein 1	CGREF1
Q99715	Collagen alpha-1(XII) chain	COL12A1
Q99727	Metalloproteinase inhibitor 4	TIMP4
Q99731	C—C motif chemokine 19	CCL19
Q99748	Neurturin	NRTN
Q99935	Proline-rich protein 1	PROL1
Q99942	E3 ubiquitin-protein ligase RNF5	RNF5
Q99944	Epidermal growth factor-like protein 8	EGFL8
Q99954	Submaxillary gland androgen-regulated protein 3A	SMR3A
Q99969	Retinoic acid receptor responder protein 2	RARRES2
Q99972	Myocilin	MYOC
Q99983	Osteomodulin	OMD
Q99985	Semaphorin-3C	SEMA3C
Q99988	Growth/differentiation factor 15	GDF15
Q9BPW4	Apolipoprotein L4	APOL4
Q9BQ08	Resistin-like beta	RETNLB
Q9BQ16	Testican-3	SPOCK3
Q9BQ51	Programmed cell death 1 ligand 2	PDCD1LG2
Q9BQB4	Sclerostin	SOST
Q9BQ14	Coiled-coil domain-containing protein 3	CCDC3
Q9BQP9	BPI fold-containing family A member 3	BPIFA3
Q9BQR3	Serine protease 27	PR5527
Q9BQY6	WAP four-disulfide core domain protein 6	WFDC6
Q9BRR6	ADP-dependent glucokinase	ADPGK
Q9BS86	Zona pellucida-binding protein 1	ZPBP
Q9BSG0	Protease-associated domain-containing protein 1	PRADC1
Q9BSG5	Retbindin	RTBDN
Q9BT30	Probable alpha-ketoglutarate-dependent dioxygenase ABH7	ALKBH7
Q9BT56	Spexin	C12orf39
Q9BT67	NEDD4 family-interacting protein 1	NDFIP1
Q9BTY2	Plasma alpha-L-fucosidase	FUCA2
Q9BU40	Chordin-like protein 1	CHRDL1
Q9BUD6	Spondin-2	SPON2
Q9BUN1	Protein MENT	MENT
Q9BUR5	Apolipoprotein O	APOO
Q9BV94	ER degradation-enhancing alpha-mannosidase-like 2	EDEM2
Q9BWP8	Collectin-11	COLEC11
Q9BWS9	Chitinase domain-containing protein 1	CHID1
Q9BX67	Junctional adhesion molecule C	JAM3
Q9BX93	Group XIIB secretory phospholipase A2-like protein	PLA2G126
Q9BXI9	Complement C1q tumor necrosis factor-related protein 6	C1QTNF6
Q9BXJ0	Complement C1q tumor necrosis factor-related protein 5	C1QTNF5
Q9BXJ1	Complement C1q tumor necrosis factor-related protein 1	C1QTNF1
Q9BXJ2	Complement C1q tumor necrosis factor-related protein 7	C1QTNF7
Q9BXJ3	Complement C1q tumor necrosis factor-related protein 4	C1QTNF4
Q9BXJ4	Complement C1q tumor necrosis factor-related protein 3	C1QTNF3
Q9BXJ5	Complement C1q tumor necrosis factor-related protein 2	C1QTNF2
Q9BXN1	Asporin	ASPN
Q9BXP8	Pappalysin-2	PAPPA2
Q9BXR6	Complement factor H-related protein 5	CFHR5
Q9BXS0	Collagen alpha-1(XXV) chain	COL25A1
Q9BXX0	EMILIN-2	EMILIN2
Q9BXY4	R-spondin-3	RSPO3
Q9BY15	EGF-like module-containing mucin-like hormone receptor-	EMR3
	like 3 subunit beta
Q9BY50	Signal peptidase complex catalytic subunit SEC11C	SEC11C
Q9BY76	Angiopoietin-related protein 4	ANGPTL4
Q9BYF1	Processed angiotensin-converting enzyme 2	ACE2
Q9BYJ0	Fibroblast growth factor-binding protein 2	FGFBP2
Q9BYW3	Beta-defensin 126	DEFB126
Q9BYX4	Interferon-induced helicase C domain-containing protein 1	IFIH1
Q9BYZ8	Regenerating islet-derived protein 4	REG4
Q9BZ76	Contactin-associated protein-like 3	CNTNAP3
Q9BZG9	Ly-6/neurotoxin-like protein 1	LYNX1
Q9BZJ3	Tryptase delta	TPSD1
Q9BZM1	Group XIIA secretory phospholipase A2	PLA2G12A
Q9BZM2	Group IIF secretory phospholipase A2	PLA2G2F
Q9BZM5	NKG2D ligand 2	ULBP2
Q9BZP6	Acidic mammalian chitinase	CHIA
Q9BZZ2	Sialoadhesin	SIGLEC1
Q9C0B6	Protein FAM5B	FAM5B
Q9GZM7	Tubulointerstitial nephritis antigen-like	TINAGL1
Q9GZN4	Brain-specific serine protease 4	PRSS22
Q9GZPO	Platelet-derived growth factor D, receptor-binding form	PDGFD
Q9GZT5	Protein Wnt-10a	WNT10A
Q9GZU5	Nyctalopin	NYX
Q9GZV7	Hyaluronan and proteoglycan link protein 2	HAPLN2
Q9GZV9	Fibroblast growth factor 23	FGF23
Q9GZX9	Twisted gastrulation protein homolog 1	TWSG1
Q9GZZ7	GDNF family receptor alpha-4	GFRA4
Q9GZZ8	Extracellular glycoprotein lacritin	LACRT
Q9H0B8	Cysteine-rich secretory protein LCCL domain-containing 2	CRISPLD2
Q9H106	Signal-regulatory protein delta	SIRPD
Q9H114	Cystatin-like 1	CSTL1
Q9H173	Nucleotide exchange factor SIL1	SIL1
Q9H1E1	Ribonuclease 7	RNASE7
Q9H1F0	WAP four-disulfide core domain protein 10A	WFDC10A
Q9H1J5	Protein Wnt-8a	WNT8A
Q9H1J7	Protein Wnt-5b	WNT5B
Q9H1M3	Beta-defensin 129	DEFB129
Q9H1M4	Beta-defensin 127	DEFB127
Q9H1Z8	Augurin	C2orf40
Q9H 239	Matrix metalloproteinase-28	MMP28
Q9H2A7	C—X—C motif chemokine 16	CXCL16
Q9H2A9	Carbohydrate sulfotransferase 8	CHST8
Q9H2R5	Kallikrein-15	KLK15
Q9H2X0	Chordin	CHRD
Q9H2X3	C-type lectin domain family 4 member M	CLEC4M
Q9H306	Matrix metalloproteinase-27	MMP27
Q9H324	A disintegrin and metalloproteinase with thrombospondin	ADAMTS10
	motifs 10
Q9H336	Cysteine-rich secretory protein LCCL domain-containing 1	CRISPLD1
Q9H3E2	Sorting nexin-25	SNX25
Q9H3R2	Mucin-13	MUC13
Q9H3U7	SPARC-related modular calcium-binding protein 2	SMOC2
Q9H3Y0	Peptidase inhibitor R3HDML	R3HDML
Q9H4A4	Aminopeptidase	BRNPEP
Q9H4F8	SPARC-related modular calcium-binding protein 1	SMOC1
Q9H4G1	Cystatin-9-like	CST9L
Q9H5V8	CUB domain-containing protein 1	CDCP1
Q9H6B9	Epoxide hydrolase 3	EPHX3
Q9H6E4	Coiled-coil domain-containing protein 134	CCDC134
Q9H741	UPF0454 protein C12orf49	C12orf49
Q9H772	Gremlin-2	GREM2
Q9H7Y0	Deleted in autism-related protein 1	CXorf36
Q9H8L6	Multimerin-2	MMRN2
Q9H955	Fukutin-related protein	FKRP
Q9HAT2	Sialate O-acetylesterase	SIAE
Q9H640	Retinoid-inducible serine carboxypeptidase	SCPEP1
Q9H663	Netrin-4	NTN4
Q9HBJ0	Placenta-specific protein 1	PLAC1
Q9HC23	Prokineticin-2	PROK2
Q9HC57	WAP four-disulfide core domain protein 1	WFDC1
Q9HC73	Cytokine receptor-like factor 2	CRLF2
Q9HC84	Mucin-5B	MUC5B
Q9HCB6	Spondin-1	SPON1
Q9HC07	Neuropeptide NPSF	NPVF
Q9HCT0	Fibroblast growth factor 22	FGF22
Q9HD89	Resistin	RETN
Q9NNX1	Tuftelin	TUFT1
Q9NNX6	CD209 antigen	CD209
Q9NP55	BPI fold-containing family A member 1	BPIFA1
Q9NP70	Ameloblastin	AMBN
Q9NP95	Fibroblast growth factor 20	FGF20
Q9NP99	Triggering receptor expressed on myeloid cells 1	TREM1
Q9NPA2	Matrix metalloproteinase-25	MMP25
Q9NPE2	Neugrin	NGRN
Q9NPH0	Lysophosphatidic acid phosphatase type 6	ACP6
Q9NPH6	Odorant-binding protein 2b	OBP2B
Q9N030	Endothelial cell-specific molecule 1	ESM1
Q9N036	Signal peptide, CUB and EGF-like domain-containing protein 2	SCUBE2
Q9N038	Serine protease inhibitor Kazal-type 5	SPINK5
Q9N076	Matrix extracellular phosphoglycoprotein	MEPE
Q9N079	Cartilage acidic protein 1	CRTAC1
Q9NR16	Scavenger receptor cysteine-rich type 1 protein M160	CD163L1
Q9NR23	Growth/differentiation factor 3	GDF3
Q9NR71	Neutral ceramidase	ASAH2
Q9NR99	Matrix-remodeling-associated protein 5	MXRA5
Q9NRA1	Platelet-derived growth factor C	PDGFC
Q9NRC9	Otoraplin	OTOR
Q9NRE1	Matrix metalloproteinase-26	MMP26
Q9NRJ3	C—C motif chemokine 28	CCL28
Q9NRM1	Enamelin	ENAM
Q9NRN5	Olfactomedin-like protein 3	OLFML3
Q9NRR1	Cytokine-like protein 1	CYTL1
Q9N515	Latent-transforming growth factor beta-binding protein 3	LTBP3
Q9N562	Thrombospondin type-1 domain-containing protein 1	THSD1
Q9N571	Gastrokine-1	GKN1
Q9N598	Semaphorin-3G	SEMA3G
Q9NSA1	Fibroblast growth factor 21	FGF21
Q9NT22	EMILIN-3	EMILIN3
Q9NTU7	Cerebellin-4	CBLN4
Q9NVR0	Kelch-like protein 11	KLHL11
Q9NWH7	Spermatogenesis-associated protein 6	SPATA6
Q9NXC2	Glucose-fructose oxidoreductase domain-containing protein 1	GFOD1
Q9NY56	Odorant-binding protein 2a	OBP2A
Q9NY84	Vascular non-inflammatory molecule 3	VNN3
Q9NZ20	Group 3 secretory phospholipase A2	PLA2G3
Q9NZC2	Triggering receptor expressed on myeloid cells 2	TREM2
Q9NZK5	Adenosine deaminase CECR1	CECR1
Q9NZK7	Group IIE secretory phospholipase A2	PLA2G2E
Q9NZP8	Complement C1r subcomponent-like protein	C1RL
Q9NZV1	Cysteine-rich motor neuron 1 protein	CRIM1
Q9NZW4	Dentin sialoprotein	DSPP
Q9P0G3	Kallikrein-14	KLK14
Q9P0W0	Interferon kappa	IFNK
Q9P218	Collagen alpha-1(XX) chain	COL20A1
Q9P2C4	Transmembrane protein 181	TMEM181
Q9P2K2	Thioredoxin domain-containing protein 16	TXNDC16
Q9P2N4	A disintegrin and metalloproteinase with thrombospondin	ADAMTS9
	motifs 9
Q9UBC7	Galanin-like peptide	GALP
Q9UBD3	Cytokine SCM-1 beta	XCL2
Q9UBD9	Cardiotrophin-like cytokine factor 1	CLCF1
Q9UBM4	Opticin	OPTC
Q9UBP4	Dickkopf-related protein 3	DKK3
Q9U606	Exostosin-like 2	EXTL2
Q9UBR5	Chemokine-like factor	CKLF
Q9UBS5	Gamma-aminobutyric acid type B receptor subunit 1	GABBR1
Q9UBT3	Dickkopf-related protein 4 short form	DKK4
Q9UBU2	Dickkopf-related protein 2	DKK2
Q9UBU3	Ghrelin-28	GHRL
Q9UBV4	Protein Wnt-16	WNT16
Q9UBX5	Fibulin-5	FBLN5
Q9UBX7	Kallikrein-11	KLK11
Q9UEF7	Klotho	KL
Q9UFP1	Protein FAM198A	FAM198A
Q9UGM3	Deleted in malignant brain tumors 1 protein	DMBT1
Q9UGM5	Fetuin-B	FETUB
Q9UGP8	Translocation protein 5EC63 homolog	5EC63
Q9UHF0	Neurokinin-B	TAC3
Q9UHF1	Epidermal growth factor-like protein 7	EGFL7
Q9UHG2	ProSAAS	PCSK1N
09UHI8	A disintegrin and metalloproteinase with thrombospondin	ADAMTS1
	motifs
1
Q9UHL4	Dipeptidyl peptidase	2	DPP7
Q9U142	Carboxypeptidase A4	CPA4
Q9UIG4	Psoriasis susceptibility 1 candidate gene 2 protein	PSORS1C2
Q9UIK5	Tomoregulin-2	TMEFF2
Q9U106	Leucyl-cystinyl aminopeptidase, pregnancy serum form	LNPEP
Q9UJA9	Ectonucleotide pyrophosphatase/phosphodiesterase family	ENPP5
	member
5
Q9UJH8	Meteorin	METRN
Q9UJJ9	N-acetylglucosamine-1-phosphotransferase subunit gamma	GNPTG
Q9UJW2	Tubulointerstitial nephritis antigen	TINAG
Q9UK05	Growth/differentiation factor 2	GDF2
Q9UK55	Protein Z-dependent protease inhibitor	SERPINA10
Q9UK85	Dickkopf-like protein 1	DKKL1
Q9UKJ1	Paired immunoglobulin-like type 2 receptor alpha	PILRA
Q9UKP4	A disintegrin and metalloproteinase with thrombospondin	ADAMTS7
	motifs 7
Q9UKP5	A disintegrin and metalloproteinase with thrombospondin	ADAMTS6
	motifs 6
09UK02	Disintegrin and metalloproteinase domain-containing	ADAM28
	protein
28
Q9UK09	Kallikrein-9	KLK9
Q9UKR0	Kallikrein-12	KLK12
Q9UKR3	Kallikrein-13	KLK13
Q9UKU9	Angiopoietin-related protein 2	ANGPTL2
Q9UKZ9	Procollagen C-endopeptidase enhancer 2	PCOLCE2
Q9UL52	Transmembrane protease serine 11E non-catalytic chain	TMPRSS11E
Q9ULC0	Endomucin	EMCN
Q9ULI3	Protein HEG homolog 1	HEG1
Q9ULZ1	Apelin-13	APLN
Q9ULZ9	Matrix metalloproteinase-17	MMP17
Q9UM21	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-	MGAT4A
	acetylglucosaminyltransferase A soluble form
Q9UM22	Mammalian ependymin-related protein 1	EPDR1
Q9UM73	ALK tyrosine kinase receptor	ALK
Q9UMD9	97 kDa linear IgA disease antigen	COL17A1
Q9UMX5	Neudesin	NENF
Q9UN73	Protocadherin alpha-6	PCDHA6
Q9UNA0	A disintegrin and metalloproteinase with thrombospondin	ADAMTS5
	motifs 5
Q9UNI1	Chymotrypsin-like elastase family member 1	CELA1
Q9UNK4	Group IID secretory phospholipase A2	PLA2G2D
Q9UP79	A disintegrin and metalloproteinase with thrombospondin	ADAMTS8
	motifs
8
Q9UPZ6	Thrombospondin type-1 domain-containing protein 7A	THSD7A
Q9U072	Pregnancy-specific beta-1-glycoprotein 11	PSG11
Q9U074	Pregnancy-specific beta-1-glycoprotein 8	PSG8
Q9U0C9	Calcium-activated chloride channel regulator 2	CLCA2
Q9U0E7	Structural maintenance of chromosomes protein 3	SMC3
Q9U0P3	Tenascin-N	TNN
Q9Y223	UDP-N-acetylglucosamine 2-epimerase	GNE
Q9Y240	C-type lectin domain family 11 member A	CLEC11A
Q9Y251	Heparanase 8 kDa subunit	HPSE
Q9Y258	C—C motif chemokine 26	CCL26
Q9Y264	Angiopoietin-4	ANGPT4
Q9Y275	Tumor necrosis factor ligand superfamily member 13b,	TNFSF136
	membrane form
Q9Y287	BRI2 intracellular domain	ITM2B
Q9Y2E5	Epididymis-specific alpha-mannosidase	MAN2B2
Q9Y334	von Willebrand factor A domain-containing protein 7	VWA7
Q9Y337	Kallikrein-5	KLK5
Q9Y3B3	Transmembrane emp24 domain-containing protein 7	TMED7
Q9Y3E2	BoIA-like protein 1	BOLA1
Q9Y426	C2 domain-containing protein 2	C2CD2
Q9Y4K0	Lysyl oxidase homolog 2	LOXL2
Q9Y4X3	C—C motif chemokine 27	CCL27
Q9Y5C1	Angiopoietin-related protein 3	ANGPTL3
Q9Y5I2	Protocadherin alpha-10	PCDHA10
Q9Y5I3	Protocadherin alpha-1	PCDHA1
Q9Y5K2	Kallikrein-4	KLK4
Q9Y5L2	Hypoxia-inducible lipid droplet-associated protein	HILPDA
Q9Y5Q5	Atrial natriuretic peptide-converting enzyme	CORIN
Q9Y5R2	Matrix metalloproteinase-24	MMP24
Q9Y5U5	Tumor necrosis factor receptor superfamily member 18	TNFRSF18
Q9Y5W5	Wnt inhibitory factor 1	WIF1
Q9Y5X9	Endothelial lipase	LIPG
Q9Y625	Secreted glypican-6	GPC6
Q9Y646	Carboxypeptidase	QCPQ
Q9Y6C2	EMILIN-1	EMILIN1
Q9Y6F9	Protein Wnt-6	WNT6
Q9Y6I9	Testis-expressed sequence 264 protein	TEX264
Q9Y6L7	Tolloid-like protein 2	TLL2
Q9Y6N3	Calcium-activated chloride channel regulator family member 3	CLCA3P
Q9Y6N6	Laminin subunit gamma-3	LAMC3
Q9Y6R7	IgGFc-binding protein	FCGBP
Q9Y6Y9	Lymphocyte antigen 96	LY96
Q9Y6Z7	Collectin-10	COLEC10

In one set of embodiments, the MCNA compound comprises two encoding polynucleotides. For example, the MCNA compound may be a palindromic coding nucleic acid (PCNA) having two encoding polynucleotides each having a polynucleotide portion that codes for the same protein.
In some embodiments, a MCNA compound comprises an encoding polynucleotide that encodes Cystic Fibrosis Transmembrane Conductance Regulator (hCFTR) mRNA, linked to a non-coding polynucleotide via a 3′ end linkage between the polynucleotides. In some embodiments, a MCNA compound comprises two or more encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one of the encoding polynucleotides encodes hCFTR. In some embodiments, a MCNA compound is a palindromic coding nucleic acid (PCNA) comprising two encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein each encoding polynucleotide codes for hCFTR. In some embodiments, a MCNA compound comprises two or more polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one polynucleotide is an encoding polynucleotide that encodes hCFTR and at least one polynucleotide acts as a protecting group.
In some embodiments, a MCNA compound comprises an encoding polynucleotide that encodes human phenylalanine hydroxylase (hPAH) mRNA, linked to a non-coding polynucleotide via a 3′ end linkage between the polynucleotides. In some embodiments, a MCNA compound comprises two or more encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one of the encoding polynucleotides encodes hPAH. In some embodiments, a MCNA compound is a palindromic coding nucleic acid (PCNA) comprising two encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein each encoding polynucleotide codes for hPAH. In some embodiments, a MCNA compound comprises two or more polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one polynucleotide is an encoding polynucleotide that encodes hPAH and at least one polynucleotide acts as a protecting group.
In some embodiments, a MCNA compound comprises an encoding polynucleotide that encodes human Ornithine transcarbamylase (hOTC) mRNA, linked to a non-coding polynucleotide via a 3′ end linkage between the polynucleotides. In some embodiments, a MCNA compound comprises two or more encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one of the encoding polynucleotides encodes hOTC. In some embodiments, a MCNA compound is a palindromic coding nucleic acid (PCNA) comprising two encoding polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein each polynucleotide codes for hOTC. In some embodiments, a MCNA compound comprises two or more polynucleotides linked via a 3′ end linkage between the polynucleotides such that the MCNA compound comprises two or more 5′ ends, wherein at least one polynucleotide is an encoding polynucleotide that encodes hOTC and at least one polynucleotide acts as a protecting group.
Bridge (w/3′-3′ Linkage)
In some embodiments, a MCNA compound comprises two or more polynucleotides wherein the 3′ ends of each polynucleotide are linked via an oligonucleotide bridge (also “bridging oligonucleotide” or “bridging olio”) comprising a 3′-3′ inverted phosphodiester linkage. In some embodiments, the oligonucleotide bridge comprises modified nucleotides. In some embodiments, the oligonucleotide bridge comprises 2′-O-methyl RNA. In some embodiments, the oligonucleotide bridge comprises DNA. In some embodiments, the oligonucleotide bridge is between 2 and 1000 nucleotides in length. In some embodiments, the oligonucleotide bridge comprises one or more active moieties that are bound to the bridge by covalent links. In some embodiments, an active moiety is a targeting group, peptide, contrast agent, small molecule, protein, DNA and/or RNA. In some embodiments, an active moiety binds a receptor ligand for a cell surface receptor. In some embodiments, the active moiety is one or more tri-antennary GalNac targeting agents.
MCNA Synthesis
In some embodiments, the present invention provides methods of synthesizing MCNA. In some embodiments, the synthesis of MCNA comprises ligating two or more polynucleotides such that the 3′ end of each polynucleotide is ligated to the 5′ end of an oligonucleotide bridge, wherein the oligonucleotide bridge comprises two 5′ ends and an internal 3′-3′ inverted phosphodiester linkage. In some embodiments, the method of synthesizing MCNA comprises the use of oligonucleotide splints complementary to regions of the two or more polynucleotides such that a ligase can join each polynucleotide to a 5′ end of an oligonucleotide bridge. In some embodiments, oligonucleotide splints are complementary to regions of the two or more polynucleotides such that a ligase joins perfect ends of each polynucleotide to a 5′ end of an oligonucleotide bridge. In some embodiments, oligonucleotide splints are complementary to regions of the two or more polynucleotides such that a ligase joins the 3′ end of each polynucleotide to a 5′ end of an oligonucleotide bridge. In some embodiments, an oligonucleotide splint comprises DNA. In some embodiments, a ligase is RNA Ligase. In some embodiments, a ligase is T4 RNA Ligase 1. In some embodiments, a ligase is T4 RNA Ligase 2.
In some embodiments, the molar ratio of polynucleotide to oligonucleotide bridge to oligonucleotide splint when synthesizing MCNA is 2:1:2. In some embodiments, the molar ratio of polynucleotide to oligonucleotide bridge when synthesizing MCNA is 2:1. In some embodiments, the molar ratio of polynucleotide to oligonucleotide splint when synthesizing MCNA is 2:2. In some embodiments, synthesis of MCNA further comprises PEG.
In some embodiments, MCNA can be prepared by splint ligation of the 3′ end of two copies of an RNA to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′ untranslated region (UTR) and a 3′ UTR flanking an RNA coding sequence is transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This transcript is then ligated in a single step to a “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt using either (A) T4 RNA ligase 1, (B) T4 RNA ligase 1+PEG 8K, or (C) T4 RNA Ligase 2 and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo. To prepare the samples for ligation, the bridging oligo is 5′-end phosphorylated in a reaction containing 50 μM oligo, ATP, 1×PNK Buffer and T4 Polynucleotide Kinase at 37° C. for 1 hour. Phosphorylated bridging oligo is then desalted using a Sephadex G-25 desalting column and hybridized to the transcript and splint in a reaction containing capped RNA transcript, 1× bridging oligo and 2× splint oligo by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction is subsequently prepared to contain a 50% diluted hybridization reaction and (A) 1×RNA ligase Buffer, ATP and T4 RNA ligase 1 (NEB), (B) 1×RNA ligase Buffer, ATP, 10% PEG and T4 RNA ligase 1 (NEB), or (C) 1×T4RNA Ligase 2 Buffer and T4 RNA ligase 2 (NEB). Each is reacted for 90 minutes at 37° C. The completed ligation reaction is then purified using an RNeasy Mini Kit (Qiagen). The purified MCNA product is subsequently treated with DNase I to remove residual bridge oligonucleotide.
In some embodiments, MCNA can be prepared by splint-independent ligation of the 3′ end of two copies of an RNA to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence.
Untranslated Regions
Typically, mRNA synthesis includes the addition of a “cap” on the 5′ end, and a “tail” on the 3′ end. The presence of the cap is important in providing resistance to nucleases found in most eukaryotic cells. The presence of a “tail” serves to protect the mRNA from exonuclease degradation.
In some embodiments, one or more polynucleotides of the MCNA include a 5′ and/or 3′ untranslated region. In some embodiments, a 5′ untranslated region (5′ UTR) includes one or more elements that affect an mRNA's stability or translation, for example, an iron responsive element. In some embodiments, a 5′ untranslated region may be between about 50 and 500 nucleotides in length.
In some embodiments, a 3′ untranslated region (3′ UTR) includes one or more of a polyadenylation signal, a binding site for proteins that affect MCNA's stability of location in a cell, or one or more binding sites for miRNAs. In some embodiments, a 3′ untranslated region may be between 50 and 500 nucleotides in length or longer. In some embodiments, a 3′ untranslated region may be between 5 and 2,000 nucleotides in length.
Exemplary 3′ and/or 5′ UTR sequences can be derived from nucleic acid molecules that are stable (e.g., globin, actin, GAPDH, tubulin, histone, or citric acid cycle enzymes) to increase the stability of the sense MCNA molecule. For example, a 5′ UTR sequence may include a partial sequence of a CMV immediate-early 1 (IE1) gene, or a fragment thereof to improve the nuclease resistance and/or improve the half-life of the polynucleotide. Also contemplated is the inclusion of a sequence encoding human growth hormone (hGH), or a fragment thereof to the 3′ end or untranslated region of the polynucleotide (e.g., MCNA) to further stabilize the polynucleotide. Generally, these modifications improve the stability and/or pharmacokinetic properties (e.g., half-life) of the polynucleotide relative to their unmodified counterparts, and include, for example modifications made to improve such polynucleotides' resistance to in vivo nuclease digestion.
3′ UTR
In some embodiments, a 3′ UTR comprises a plurality of multi-A segments with spacers in between. In some embodiments, spacers comprise DNA, RNA and/or modified bases. In some embodiments, each of the multi-A segments comprises 8-50 consecutive adenosines. In some embodiments, the plurality of multi-A segments range from 1-100 in number. In some embodiments, the spacers are of varying lengths ranging from 5-100. In some embodiments, a 3′ UTR comprises a pseudoknot structure. A pseudoknot can be defined as an RNA structure minimally composed of two helical segments connected by single stranded regions or loops (Staple, D. W. et al., PLoS Biology, 2005, 3, e213). They are predominantly formed through secondary structures such as hairpin or stem loops and a distal single strand region. In some embodiments, a 3′ UTR comprises a “kissing loop” sequence motif. Broadly defined, a kissing loop can be described as the structure formed when unpaired nucleotides in a stem/hairpin loop of one RNA molecule base pair with unpaired nucleotides of a second stem/hairpin loop of a separate RNA molecule. In some embodiments, a 3′ UTR is not followed with a polyadenylation (poly-A) tail. In some embodiments, a 3′ UTR binds to poly-A binding proteins (PABPs).
In some embodiments, MCNA include a 3′ poly(A) tail structure. In some embodiments, a poly-A tail is 25-5,000 nucleotides in length. A poly-A tail on the 3′ terminus of MCNA typically includes about 10 to 300 adenosine nucleotides (e.g., about 10 to 200 adenosine nucleotides, about 10 to 150 adenosine nucleotides, about 10 to 100 adenosine nucleotides, about 20 to 70 adenosine nucleotides, or about 20 to 60 adenosine nucleotides). In some embodiments, mRNAs include a 3′ poly(C) tail structure. A suitable poly-C tail on the 3′ terminus of MCNA typically include about 10 to 200 cytosine nucleotides (e.g., about 10 to 150 cytosine nucleotides, about 10 to 100 cytosine nucleotides, about 20 to 70 cytosine nucleotides, about 20 to 60 cytosine nucleotides, or about 10 to 40 cytosine nucleotides). The poly-C tail may be added to the poly-A tail or may substitute the poly-A tail.
Typically, the presence of a “tail” serves to protect the MCNA from exonuclease degradation. The poly A tail is thought to stabilize natural messengers and synthetic sense MCNA. Therefore, in certain embodiments a long poly A tail can be added to an MCNA molecule thus rendering the MCNA more stable. Poly A tails can be added using a variety of art-recognized techniques. For example, long poly A tails can be added to synthetic or in vitro transcribed RNA using poly A polymerase (Yokoe, et al. Nature Biotechnology. 1996; 14: 1252-1256). A transcription vector can also encode long poly A tails. In addition, poly A tails can be added by transcription directly from PCR products. Poly A may also be ligated to the 3′ end of a sense RNA with RNA ligase (see, e.g., Molecular Cloning A Laboratory Manual, 2nd Ed., ed. by Sambrook, Fritsch and Maniatis (Cold Spring Harbor Laboratory Press: 1991 edition)).
In some embodiments, one or more polynucleotides of the MCNA includes a 3′ poly(A) tail structure. Typically, the length of the poly-A tail can be at least about 10, 50, 100, 200, 300, 400 at least 500 nucleotides. In some embodiments, a poly-A tail on the 3′ terminus of MCNA typically includes about 10 to 300 adenosine nucleotides (e.g., about 10 to 200 adenosine nucleotides, about 10 to 150 adenosine nucleotides, about 10 to 100 adenosine nucleotides, about 20 to 70 adenosine nucleotides, or about 20 to 60 adenosine nucleotides). In some embodiments, MCNA include a 3′ poly-C tail structure. A suitable poly-C tail on the 3′ terminus of MCNA typically include about 10 to 200 cytosine nucleotides (e.g., about 10 to 150 cytosine nucleotides, about 10 to 100 cytosine nucleotides, about 20 to 70 cytosine nucleotides, about 20 to 60 cytosine nucleotides, or about 10 to 40 cytosine nucleotides). The poly-C tail may be added to the poly-A tail or may substitute the poly-A tail.
In some embodiments, the length of the poly-A or poly-C tail is adjusted to control the stability of a modified sense MCNA molecule of the invention and, thus, the transcription of protein that is coded for by one or more of the encoding polynucleotides of the MCNA. For example, since the length of the poly-A tail can influence the half-life of a sense MCNA molecule, the length of the poly-A tail can be adjusted to modify the level of resistance of the MCNA to nucleases and thereby control the time course of polynucleotide expression and/or polypeptide production in a target cell.
5′ UTR
In some embodiments, MCNA include a 5′ cap structure. A 5′ cap is typically added as follows: first, an RNA terminal phosphatase removes one of the terminal phosphate groups from the 5′ nucleotide, leaving two terminal phosphates; guanosine triphosphate (GTP) is then added to the terminal phosphates via a guanylyl transferase, producing a 5′5′5 triphosphate linkage; and the 7-nitrogen of guanine is then methylated by a methyltransferase. Examples of cap structures include, but are not limited to, m7G(5′)ppp (5′(A,G(5′)ppp(5′)A and G(5′)ppp(5′)G.
Naturally occurring cap structures comprise a 7-methyl guanosine that is linked via a triphosphate bridge to the 5′-end of the first transcribed nucleotide, resulting in a dinucleotide cap of m⁷G(5′)ppp(5′)N, where N is any nucleoside. In vivo, the cap is added enzymatically. The cap is added in the nucleus and is catalyzed by the enzyme guanylyl transferase. The addition of the cap to the 5′ terminal end of RNA occurs immediately after initiation of transcription. The terminal nucleoside is typically a guanosine, and is in the reverse orientation to all the other nucleotides, i.e., G(5′)ppp(5′)GpNpNp.
One cap for MCNA produced by in vitro transcription is m⁷G(5′)ppp(5′)G, which has been used as the dinucleotide cap in transcription with T7 or SP6 RNA polymerase in vitro to obtain MCNA having a cap structure in their 5′-termini. A method for the in vitro synthesis of capped MCNA employs a pre-formed dinucleotide of the form m⁷G(5′)ppp(5′)G (“m⁷GpppG”) as an initiator of transcription.
To date, a usual form of a synthetic dinucleotide cap used in in vitro translation experiments is the Anti-Reverse Cap Analog (“ARCA”) or modified ARCA, which is generally a modified cap analog in which the 2′ or 3′ OH group is replaced with —OCH₃.
Additional cap analogs include, but are not limited to, a chemical structures selected from the group consisting of m⁷GpppG, m⁷GpppA, m⁷GpppC; unmethylated cap analogs (e.g., GpppG); dimethylated cap analog (e.g., m^2,7GpppG), trimethylated cap analog (e.g., m^2,2,7GpppG), dimethylated symmetrical cap analogs (e.g., m⁷Gpppm⁷G), or anti reverse cap analogs (e.g., ARCA; m^{7 2′Ome}GpppG, m^72′dGpppG, m^7,3′OmeGpppG, m^7,3′dm GpppG and their tetraphosphate derivatives) (see, e.g., Jemielity, J. et al., “Novel ‘anti-reverse’ cap analogs with superior translational properties”, RNA, 9: 1108-1122 (2003)).
In some embodiments, a suitable cap is a 7-methyl guanylate (“m⁷G”) linked via a triphosphate bridge to the 5′-end of the first transcribed nucleotide, resulting in m⁷G(5′)ppp(5′)N, where N is any nucleoside. A preferred embodiment of a m⁷G cap utilized in embodiments of the invention is m⁷G(5′)ppp(5′)G.
In some embodiments, the cap is a Cap0 structure. Cap0 structures lack a 2′-O-methyl residue of the ribose attached to bases 1 and 2. In some embodiments, the cap is a Cap1 structure. Cap1 structures have a 2′-O-methyl residue at base 2. In some embodiments, the cap is a Cap2 structure. Cap2 structures have a 2′-O-methyl residue attached to both bases 2 and 3.
A variety of m⁷G cap analogs are known in the art, many of which are commercially available. These include the m⁷GpppG described above, as well as the ARCA 3′-OCH₃and 2′-OCH₃cap analogs (Jemielity, J. et al., RNA, 9: 1108-1122 (2003)). Additional cap analogs for use in embodiments of the invention include N7-benzylated dinucleoside tetraphosphate analogs (described in Grudzien, E. et al., RNA, 10: 1479-1487 (2004)), phosphorothioate cap analogs (described in Grudzien-Nogalska, E., et al., RNA, 13: 1745-1755 (2007)), and cap analogs (including biotinylated cap analogs) described in U.S. Pat. Nos. 8,093,367 and 8,304,529, incorporated by reference herein.
Nucleotide Modifications
In some embodiments, MCNA according to the present invention may be synthesized as unmodified or modified nucleic acid. Typically, nucleic acids are modified to enhance stability. Modifications of MCNA can include, for example, modifications of the nucleotides of the MCNA. A modified MCNA according to the invention can thus include, for example, backbone modifications, sugar modifications or base modifications. In some embodiments, MCNA may be synthesized from naturally occurring nucleotides and/or nucleotide analogues (modified nucleotides) including, but not limited to, purines (adenine (A), guanine (G)) or pyrimidines (thymine (T), cytosine (C), uracil (U)), and as modified nucleotides analogues or derivatives of purines and pyrimidines, such as, e.g. 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ψU), and 1-methyl-pseudouridine, 1-methyl-adenine, 2-methyl-adenine, 2-methylthio-N-6-isopentenyl-adenine, N6-methyl-adenine, N6-isopentenyl-adenine, 2-thio-cytosine, 3-methyl-cytosine, 4-acetyl-cytosine, 5-methyl-cytosine, 2,6-diaminopurine, 1-methyl-guanine, 2-methyl-guanine, 2,2-dimethyl-guanine, 7-methyl-guanine, inosine, 1-methyl-inosine, pseudouracil (5-uracil), dihydro-uracil, 2-thio-uracil, 4-thio-uracil, 5-carboxymethylaminomethyl-2-thio-uracil, 5-(carboxyhydroxymethyl)-uracil, 5-fluoro-uracil, 5-bromo-uracil, 5-carboxymethylaminomethyl-uracil, 5-methyl-2-thio-uracil, 5-methyl-uracil, N-uracil-5-oxyacetic acid methyl ester, 5-methylaminomethyl-uracil, 5-methoxyaminomethyl-2-thio-uracil, 5′-methoxycarbonylmethyl-uracil, 5-methoxy-uracil, uracil-5-oxyacetic acid methyl ester, uracil-5-oxyacetic acid (v), 1-methyl-pseudouracil, queosine, .beta.-D-mannosyl-queosine, wybutoxosine, and phosphoramidates, phosphorothioates, peptide nucleotides, methylphosphonates, 7-deazaguanosine, 5-methylcytosine and inosine. The preparation of such analogues is known to a person skilled in the art e.g., from the U.S. Pat. Nos. 4,373,071, 4,401,796, 4,415,732, 4,458,066, 4,500,707, 4,668,777, 4,973,679, 5,047,524, 5,132,418, 5,153,319, 5,262,530 and 5,700,642, the disclosures of which are incorporated by reference in their entirety.
In some embodiments, MCNA of the of the present invention comprise encoding polynucleotides that comprise one or more modified nucleotides. In some embodiments, the one or more modified nucleotides are selected from the group consisting of 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ψU), and 1-methyl-pseudouridine. In some embodiments, the modified nucleotides substitute 1-100% of corresponding native bases. In some embodiments, at least 25% of uridines are replaced with 2-thiouridines. In some embodiments, 100% cytidines are replaced with 5-methylcytidines. In some embodiments, modified nucleotides are further modified with a 4′-thio substitution on the ribose ring. In some embodiments, native nucleotides are modified with a 4′-thio substitution on the ribose ring.
In some embodiments, MCNA may contain nucleic acid backbone modifications. Typically, a backbone modification is a modification in which the phosphates of the backbone of the nucleotides contained in the MCNA are modified chemically. Exemplary backbone modifications typically include, but are not limited to, modifications from the group consisting of methylphosphonates, methylphosphoramidates, phosphoramidates, phosphorothioates (e.g. cytidine 5′-O-(1-thiophosphate)), boranophosphates, positively charged guanidinium groups etc., which means by replacing the phosphodiester linkage by other anionic, cationic or neutral groups.
In some embodiments, MCNA may contain sugar modifications. A typical sugar modification is a chemical modification of the sugar of the nucleotides it contains including, but not limited to, sugar modifications chosen from the group consisting of 2′-deoxy-T-fluoro-oligoribonucleotide (2′-fluoro-2′-deoxycytidine 5′-triphosphate, 2′-fluoro-2′-deoxyuridine 5′-triphosphate), 2′-deoxy-T-deamine-oligoribonucleotide (2′-amino-2′-deoxycytidine 5′-triphosphate, 2′-amino-2′-deoxyuridine 5′-triphosphate), 2′-O-alkyloligoribonucleotide, 2′-deoxy-2′-C-alkyloligoribonucleotide (2′-O-methylcytidine 5′-triphosphate, 2′-methyluridine 5′-triphosphate), 2′-C-alkyloligoribonucleotide, and isomers thereof (2′-aracytidine 5′-triphosphate, 2′-arauridine 5′-triphosphate), or azidotriphosphates (2′-azido-T-deoxycytidine 5′-triphosphate, 2′-azido-T-deoxyuridine 5′-triphosphate).
In some embodiments, MCNA may contain modifications of the bases of the nucleotides (base modifications). A modified nucleotide which contains a base modification is also called a base-modified nucleotide. Examples of such base-modified nucleotides include, but are not limited to, 2-amino-6-chloropurine riboside 5′-triphosphate, 2-aminoadenosine 5′-triphosphate, 2-thiocytidine 5′-triphosphate, 2-thiouridine 5′-triphosphate, 4-thiouridine 5′-triphosphate, 5-aminoallylcytidine 5′-triphosphate, 5-aminoallyluridine 5′-triphosphate, 5-bromocytidine 5′-triphosphate, 5-bromouridine 5′-triphosphate, 5-iodocytidine 5′-triphosphate, 5-iodouridine 5′-triphosphate, 5-methylcytidine 5′-triphosphate, 5-methyluridine 5′-triphosphate, 6-azacytidine 5′-triphosphate, 6-azauridine 5′-triphosphate, 6-chloropurine riboside 5′-triphosphate, 7-deazaadenosine 5′-triphosphate, 7-deazaguanosine 5′-triphosphate, 8-azaadenosine 5′-triphosphate, 8-azidoadenosine 5′-triphosphate, benzimidazole riboside 5′-triphosphate, N1-methyladenosine 5′-triphosphate, N1-methylguanosine 5′-triphosphate, N6-methyladenosine 5′-triphosphate, O6-methylguanosine 5′-triphosphate, pseudouridine 5′-triphosphate, puromycin 5′-triphosphate or xanthosine 5′-triphosphate. In some embodiments, MCNA comprises modified bases selected from 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (′PU), and 1-methyl-pseudouridine.

Delivery Vehicles

According to the present invention, MCNA as described herein may be delivered as naked polynucleotides or via delivery vehicles. As used herein, the terms “delivery vehicle”, “transfer vehicle”, “nanoparticle” or grammatical equivalent, are used interchangeably.
In some embodiments, MCNA may be delivered via a single delivery vehicle. In some embodiments, MCNA may be delivered via one or more delivery vehicles each of a different composition. According to various embodiments, suitable delivery vehicles include, but are not limited to polymer based carriers, such as polyethyleneimine (PEI), lipid nanoparticles and liposomes, nanoliposomes, ceramide-containing nanoliposomes, proteoliposomes, both natural and synthetically-derived exosomes, natural, synthetic and semi-synthetic lamellar bodies, nanoparticulates, calcium phosphor-silicate nanoparticulates, calcium phosphate nanoparticulates, silicon dioxide nanoparticulates, nanocrystalline particulates, semiconductor nanoparticulates, poly(D-arginine), sol-gels, nanodendrimers, starch-based delivery systems, micelles, emulsions, niosomes, multi-domain-block polymers (vinyl polymers, polypropyl acrylic acid polymers, dynamic polyconjugates), dry powder formulations, plasmids, viruses, calcium phosphate nucleotides, aptamers, peptides and other vectorial tags.
Liposomal Delivery Vehicles
In some embodiments, a suitable delivery vehicle is a liposomal delivery vehicle, e.g., a lipid nanoparticle. As used herein, liposomal delivery vehicles, e.g., lipid nanoparticles, are usually characterized as microscopic vesicles having an interior aqua space sequestered from an outer medium by a membrane of one or more bilayers. Bilayer membranes of liposomes are typically formed by amphiphilic molecules, such as lipids of synthetic or natural origin that comprise spatially separated hydrophilic and hydrophobic domains (Lasic, Trends Biotechnol., 16: 307-321, 1998). Bilayer membranes of the liposomes can also be formed by amphophilic polymers and surfactants (e.g., polymerosomes, niosomes, etc.). In the context of the present invention, a liposomal delivery vehicle typically serves to transport a desired MCNA to a target cell or tissue.
Cationic Lipids
In some embodiments, liposomes may comprise one or more cationic lipids. As used herein, the phrase “cationic lipid” refers to any of a number of lipid species that have a net positive charge at a selected pH, such as physiological pH. Several cationic lipids have been described in the literature, many of which are commercially available. Particularly suitable cationic lipids for use in the compositions and methods of the invention include those described in international patent publications WO 2010/053572 (and particularly, CI 2-200 described at paragraph [00225]) and WO 2012/170930, both of which are incorporated herein by reference. In certain embodiments, the compositions and methods of the invention employ a lipid nanoparticles comprising an ionizable cationic lipid described in U.S. provisional patent application 61/617,468, filed Mar. 29, 2012 (incorporated herein by reference), such as, e.g, (15Z, 18Z)—N,N-dimethyl-6-(9Z, 12Z)-octadeca-9, 12-dien-1-yl)tetracosa-15,18-dien-1-amine (HGT5000), (15Z, 18Z)—N,N-dimethyl-6-((9Z, 12Z)-octadeca-9, 12-dien-1-yl)tetracosa-4,15,18-trien-1-amine (HGT5001), and (15Z,18Z)—N,N-dimethyl-6-((9Z, 12Z)-octadeca-9, 12-dien-1-yl)tetracosa-5, 15, 18-trien-1-amine (HGT5002).
In some embodiments, provided liposomes include a cationic lipid described in WO 2013/063468 and in U.S. provisional application entitled “Lipid Formulations for Delivery of Messenger RNA” filed concurrently with the present application on even date, both of which are incorporated by reference herein.
In some embodiments, a cationic lipid comprises a compound of formula I-c1-a:
or a pharmaceutically acceptable salt thereof, wherein:
each R²independently is hydrogen or C_1-3alkyl;
each q independently is 2 to 6;
each R′ independently is hydrogen or C_1-3alkyl;
and each R^Lindependently is C_8-12alkyl.
In some embodiments, each R²independently is hydrogen, methyl or ethyl. In some embodiments, each R²independently is hydrogen or methyl. In some embodiments, each R²is hydrogen.
In some embodiments, each q independently is 3 to 6. In some embodiments, each q independently is 3 to 5. In some embodiments, each q is 4.
In some embodiments, each R′ independently is hydrogen, methyl or ethyl. In some embodiments, each R′ independently is hydrogen or methyl. In some embodiments, each R′ independently is hydrogen.
In some embodiments, each R^Lindependently is C_8-12alkyl. In some embodiments, each R^Lindependently is n-C_8-12alkyl. In some embodiments, each R^Lindependently is C_9-11alkyl. In some embodiments, each R^Lindependently is n-C_9-11alkyl. In some embodiments, each R^Lindependently is C₁₀alkyl. In some embodiments, each R^Lindependently is n-C₁₀alkyl.
In some embodiments, each R²independently is hydrogen or methyl; each q independently is 3 to 5; each R′ independently is hydrogen or methyl; and each R^Lindependently is C_8-12alkyl.
In some embodiments, each R²is hydrogen; each q independently is 3 to 5; each R′ is hydrogen; and each R^Lindependently is C_8-12alkyl.
In some embodiments, each R²is hydrogen; each q is 4; each R′ is hydrogen; and each R^Lindependently is C_8-12alkyl.
In some embodiments, a cationic lipid comprises a compound of formula I-g:
or a pharmaceutically acceptable salt thereof, wherein each R^Lindependently is C_8-12alkyl. In some embodiments, each R^Lindependently is n-C_8-12alkyl. In some embodiments, each R^Lindependently is C_9-11alkyl. In some embodiments, each R^Lindependently is n-C_9-11alkyl. In some embodiments, each R^Lindependently is C₁₀alkyl. In some embodiments, each R^Lis n-C₁₀alkyl.
In particular embodiments, provided liposomes include a cationic lipid cKK-E12, or (3,6-bis(4-(bis(2-hydroxydodecyl)amino)butyl)piperazine-2,5-dione). The structure of cKK-E12 is shown below:
Additional exemplary cationic lipids include those of formula I:
and pharmaceutically acceptable salts thereof,
wherein,
R is
R is
R is
or
R is
(see, e.g., Fenton, Owen S., et al. “Bioinspired Alkenyl Amino Alcohol Ionizable Lipid Materials for Highly Potent In Vivo mRNA Delivery.” Advanced materials (2016)).
In some embodiments, the one or more cationic lipids may be N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride or “DOTMA” (Feigner et al. (Proc. Nat'l Acad. Sci. 84, 7413 (1987); U.S. Pat. No. 4,897,355). DOTMA can be formulated alone or can be combined with the neutral lipid, dioleoylphosphatidyl-ethanolamine or “DOPE” or other cationic or non-cationic lipids into a liposomal transfer vehicle or a lipid nanoparticle, and such liposomes can be used to enhance the delivery of nucleic acids into target cells. Other suitable cationic lipids include, for example, 5-carboxyspermylglycinedioctadecylamide or “DOGS,” 2,3-dioleyloxy-N-[2(spermine-carboxamido)ethyl]-N,N-dimethyl-1-propanaminium or “DOSPA” (Behr et al. Proc. Nat.'l Acad. Sci. 86, 6982 (1989); U.S. Pat. Nos. 5,171,678; 5,334,761), 1,2-Dioleoyl-3-Dimethylammonium-Propane or “DODAP”, 1,2-Dioleoyl-3-Trimethylammonium-Propane or “DOTAP”.
Additional exemplary cationic lipids also include 1,2-distearyloxy-N,N-dimethyl-3-aminopropane or “DSDMA”, 1,2-dioleyloxy-N,N-dimethyl-3-aminopropane or “DODMA”, 1,2-dilinoleyloxy-N,N-dimethyl-3-aminopropane or “DLinDMA”, 1,2-dilinolenyloxy-N,N-dimethyl-3-aminopropane or “DLenDMA”, N-dioleyl-N,N-dimethylammonium chloride or “DODAC”, N,N-distearyl-N,N-dimethylarnrnonium bromide or “DDAB”, N-(1,2-dimyristyloxyprop-3-yl)-N,N-dimethyl-N-hydroxyethyl ammonium bromide or “DMRIE”, 3-dimethylamino-2-(cholest-5-en-3-beta-oxybutan-4-oxy)-1-(cis,cis-9,12-octadecadienoxy)propane or “CLinDMA”, 2-[5′-(cholest-5-en-3-beta-oxy)-3′-oxapentoxy)-3-dimethy 1-1-(cis,cis-9′,1-2′-octadecadienoxy)propane or “CpLinDMA”, N,N-dimethyl-3,4-dioleyloxybenzylamine or “DMOBA”, 1,2-N,N′-dioleylcarbamyl-3-dimethylaminopropane or “DOcarbDAP”, 2,3-Dilinoleoyloxy-N,N-dimethylpropylamine or “DLinDAP”, 1,2-N,M-Dilinoleylcarbamyl-3-dimethylaminopropane or “DLincarbDAP”, 1,2-Dilinoleoylcarbamyl-3-dimethylaminopropane or “DLinCDAP”, 2,2-dilinoleyl-4-dimethylaminomethyl-[1,3]-dioxolane or “DLin--DMA”, 2,2-dilinoleyl-4-dimethylaminoethyl-[1,3]-dioxolane or “DLin-K-XTC2-DMA”, and 2-(2,2-di((9Z,12Z)-octadeca-9,12-dien-1-yl)-1,3-dioxolan-4-yl)-N,N-dimethylethanamine (DLin-KC2-DMA)) (See, WO 2010/042877; Semple et al., Nature Biotech. 28: 172-176 (2010)), or mixtures thereof. (Heyes, J., et al., J Controlled Release 107: 276-287 (2005); Morrissey, D V., et al., Nat. Biotechnol. 23(8): 1003-1007 (2005); PCT Publication WO2005/121348A1). In some embodiments, one or more of the cationic lipids comprise at least one of an imidazole, dialkylamino, or guanidinium moiety.
In some embodiments, the one or more cationic lipids may be chosen from XTC (2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-dioxolane), MC3 (((6Z,9Z,28Z,31Z)-heptatriaconta-6,9,28,31-tetraen-19-yl 4-(dimethylamino)butanoate), ALNY-100 ((3aR,5s,6aS)-N,N-dimethyl-2,2-di((9Z,12Z)-octadeca-9,12-dienyl)tetrahydro-3aH-cyclopenta[d][1,3]dioxol-5-amine)), NC98-5 (4,7,13-tris(3-oxo-3-(undecylamino)propyl)-N1,N16-diundecyl-4,7,10,13-tetraazahexadecane-1,16-diamide), DODAP (1,2-dioleyl-3-dimethylammonium propane), HGT4003 (WO 2012/170889, the teachings of which are incorporated herein by reference in their entirety), ICE (WO 2011/068810, the teachings of which are incorporated herein by reference in their entirety), HGT5000 (U.S. Provisional Patent Application No. 61/617,468, the teachings of which are incorporated herein by reference in their entirety) or HGT5001 (cis or trans) (Provisional Patent Application No. 61/617,468), aminoalcohol lipidoids such as those disclosed in WO2010/053572, DOTAP (1,2-dioleyl-3-trimethylammonium propane), DOTMA (1,2-di-O-octadecenyl-3-trimethylammonium propane), DLinDMA (Heyes, J.; Palmer, L.; Bremner, K.; MacLachlan, I. “Cationic lipid saturation influences intracellular delivery of encapsulated nucleic acids” J. Contr. Rel. 2005, 107, 276-287), DLin-KC2-DMA (Semple, S. C. et al. “Rational Design of Cationic Lipids for siRNA Delivery” Nature Biotech. 2010, 28, 172-176), C12-200 (Love, K. T. et al. “Lipid-like materials for low-dose in vivo gene silencing” PNAS 2010, 107, 1864-1869).
In some embodiments, the percentage of cationic lipid in a liposome may be greater than 10%, greater than 20%, greater than 30%, greater than 40%, greater than 50%, greater than 60%, or greater than 70%. In some embodiments, cationic lipid(s) constitute(s) about 30-50% (e.g., about 30-45%, about 30-40%, about 35-50%, about 35-45%, or about 35-40%) of the liposome by weight. In some embodiments, the cationic lipid (e.g., cKK-E12) constitutes about 30%, about 35%, about 40%, about 45%, or about 50% of the liposome by molar ratio.
Non-Cationic/Helper Lipids
In some embodiments, provided liposomes contain one or more non-cationic (“helper”) lipids. As used herein, the phrase “non-cationic lipid” refers to any neutral, zwitterionic or anionic lipid. As used herein, the phrase “anionic lipid” refers to any of a number of lipid species that carry a net negative charge at a selected H, such as physiological pH. Non-cationic lipids include, but are not limited to, distearoylphosphatidylcholine (DSPC), dioleoylphosphatidylcholine (DOPC), dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylglycerol (DOPG), dipalmitoylphosphatidylglycerol (DPPG), dioleoylphosphatidylethanolamine (DOPE), palmitoyloleoylphosphatidylcholine (POPC), palmitoyloleoyl-phosphatidylethanolamine (POPE), dioleoyl-phosphatidylethanolamine 4-(N-maleimidomethyl)-cyclohexane-1-carboxylate (DOPE-mal), dipalmitoyl phosphatidyl ethanolamine (DPPE), dimyristoylphosphoethanolamine (DMPE), distearoyl-phosphatidylethanolamine (DSPE), 16-O-monomethyl PE, 16-O-dimethyl PE, 18-1-trans PE, 1-stearoyl-2-oleoyl-phosphatidyethanolamine (SOPE), or a mixture thereof.
In some embodiments, such non-cationic lipids may be used alone, but are preferably used in combination with other excipients, for example, cationic lipids. In some embodiments, the non-cationic lipid may comprise a molar ratio of about 5% to about 90%, or about 10% to about 70% of the total lipid present in a liposome. In some embodiments, a non-cationic lipid is a neutral lipid, i.e., a lipid that does not carry a net charge in the conditions under which the composition is formulated and/or administered. In some embodiments, the percentage of non-cationic lipid in a liposome may be greater than 5%, greater than 10%, greater than 20%, greater than 30%, or greater than 40%.
Cholesterol-Based Lipids
In some embodiments, provided liposomes comprise one or more cholesterol-based lipids. For example, suitable cholesterol-based cationic lipids include, for example, DC-Choi (N,N-dimethyl-N-ethylcarboxamidocholesterol), 1,4-bis(3-N-oleylamino-propyl)piperazine (Gao, et al. Biochem. Biophys. Res. Comm. 179, 280 (1991); Wolf et al. BioTechniques 23, 139 (1997); U.S. Pat. No. 5,744,335), or ICE. In some embodiments, the cholesterol-based lipid may comprise a molar ration of about 2% to about 30%, or about 5% to about 20% of the total lipid present in a liposome. In some embodiments, The percentage of cholesterol-based lipid in the lipid nanoparticle may be greater than 5, %, 10%, greater than 20%, greater than 30%, or greater than 40%.
PEGylated Lipids
In some embodiments, provided liposomes comprise one or more PEGylated lipids. For example, the use of polyethylene glycol (PEG)-modified phospholipids and derivatized lipids such as derivatized ceramides (PEG-CER), including N-Octanoyl-Sphingosine-1-[Succinyl(Methoxy Polyethylene Glycol)-2000] (C8 PEG-2000 ceramide) is also contemplated by the present invention in combination with one or more of the cationic and, in some embodiments, other lipids together which comprise the liposome. Contemplated PEG-modified lipids include, but are not limited to, a polyethylene glycol chain of up to 5 kDa in length covalently attached to a lipid with alkyl chain(s) of C6-C20 length. In some embodiments, a PEG-modified or PEGylated lipid is PEGylated cholesterol or PEG-2K. The addition of such components may prevent complex aggregation and may also provide a means for increasing circulation lifetime and increasing the delivery of the lipid-nucleic acid composition to the target cell, (Klibanov et al. (1990) FEBS Letters, 268 (1): 235-237), or they may be selected to rapidly exchange out of the formulation in vivo (see U.S. Pat. No. 5,885,613).
In some embodiments, particularly useful exchangeable lipids are PEG-ceramides having shorter acyl chains (e.g., C14 or C18). The PEG-modified phospholipid and derivatized lipids of the present invention may comprise a molar ratio from about 0% to about 15%, about 0.5% to about 15%, about 1% to about 15%, about 4% to about 10%, or about 2% of the total lipid present in the liposome.
According to various embodiments, the selection of cationic lipids, non-cationic lipids and/or PEG-modified lipids which comprise the lipid nanoparticle, as well as the relative molar ratio of such lipids to each other, is based upon the characteristics of the selected lipid(s), the nature of the intended target cells, the characteristics of the MCNA to be delivered. Additional considerations include, for example, the saturation of the alkyl chain, as well as the size, charge, pH, pKa, fusogenicity and toxicity of the selected lipid(s). Thus the molar ratios may be adjusted accordingly.
Formation of Liposomes
The liposomal transfer vehicles for use in the compositions of the invention can be prepared by various techniques which are presently known in the art. The liposomes for use in provided compositions can be prepared by various techniques which are presently known in the art. For example, multilamellar vesicles (MLV) may be prepared according to conventional techniques, such as by depositing a selected lipid on the inside wall of a suitable container or vessel by dissolving the lipid in an appropriate solvent, and then evaporating the solvent to leave a thin film on the inside of the vessel or by spray drying. An aqueous phase may then added to the vessel with a vortexing motion which results in the formation of MLVs. Unilamellar vesicles (ULV) can then be formed by homogenization, sonication or extrusion of the multilamellar vesicles. In addition, unilamellar vesicles can be formed by detergent removal techniques.
In certain embodiments, provided compositions comprise a liposome wherein the MCNA is associated on both the surface of the liposome and encapsulated within the same liposome. For example, during preparation of the compositions of the present invention, cationic liposomes may associate with the MCNA through electrostatic interactions. For example, during preparation of the compositions of the present invention, cationic liposomes may associate with the MCNA through electrostatic interactions.
In some embodiments, the compositions and methods of the invention comprise MCNA encapsulated in a liposome. In some embodiments, the one or more MCNA species may be encapsulated in the same liposome. In some embodiments, the one or more MCNA species may be encapsulated in different liposomes. In some embodiments, the MCNA is encapsulated in one or more liposomes, which differ in their lipid composition, molar ratio of lipid components, size, charge (Zeta potential), targeting ligands and/or combinations thereof. In some embodiments, the one or more liposome may have a different composition of cationic lipids, neutral lipid, PEG-modified lipid and/or combinations thereof. In some embodiments the one or more liposomes may have a different molar ratio of cationic lipid, neutral lipid, cholesterol and PEG-modified lipid used to create the liposome.
The process of incorporation of a desired MCNA into a liposome is often referred to as “loading”. Exemplary methods are described in Lasic, et al., FEBS Lett., 312: 255-258, 1992, which is incorporated herein by reference. The liposome-incorporated nucleic acids may be completely or partially located in the interior space of the liposome, within the bilayer membrane of the liposome, or associated with the exterior surface of the liposome membrane. The incorporation of a nucleic acid into liposomes is also referred to herein as “encapsulation” wherein the nucleic acid is entirely contained within the interior space of the liposome. The purpose of incorporating a MCNA into a transfer vehicle, such as a liposome, is often to protect the nucleic acid from an environment which may contain enzymes or chemicals that degrade nucleic acids and/or systems or receptors that cause the rapid excretion of the nucleic acids. Accordingly, in some embodiments, a suitable delivery vehicle is capable of enhancing the stability of the MCNA contained therein and/or facilitate the delivery of MCNA to the target cell or tissue.
Liposome Size
Suitable liposomes in accordance with the present invention may be made in various sizes. In some embodiments, provided liposomes may be made smaller than previously known mRNA encapsulating liposomes. In some embodiments, decreased size of liposomes is associated with more efficient delivery of MCNA. Selection of an appropriate liposome size may take into consideration the site of the target cell or tissue and to some extent the application for which the liposome is being made.
In some embodiments, an appropriate size of liposome is selected to facilitate systemic distribution of polypeptide encoded by the MCNA. In some embodiments, it may be desirable to limit transfection of the MCNA to certain cells or tissues. For example, to target hepatocytes a liposome may be sized such that its dimensions are smaller than the fenestrations of the endothelial layer lining hepatic sinusoids in the liver; in such cases the liposome could readily penetrate such endothelial fenestrations to reach the target hepatocytes.
Alternatively or additionally, a liposome may be sized such that the dimensions of the liposome are of a sufficient diameter to limit or expressly avoid distribution into certain cells or tissues. For example, a liposome may be sized such that its dimensions are larger than the fenestrations of the endothelial layer lining hepatic sinusoids to thereby limit distribution of the liposomes to hepatocytes.
In some embodiments, the size of a liposome is determined by the length of the largest diameter of the liposome particle. In some embodiments, a suitable liposome has a size no greater than about 250 nm (e.g., no greater than about 225 nm, 200 nm, 175 nm, 150 nm, 125 nm, 100 nm, 75 nm, or 50 nm). In some embodiments, a suitable liposome has a size ranging from about 10-250 nm (e.g., ranging from about 10-225 nm, 10-200 nm, 10-175 nm, 10-150 nm, 10-125 nm, 10-100 nm, 10-75 nm, or 10-50 nm). In some embodiments, a suitable liposome has a size ranging from about 100-250 nm (e.g., ranging from about 100-225 nm, 100-200 nm, 100-175 nm, 100-150 nm). In some embodiments, a suitable liposome has a size ranging from about 10-100 nm (e.g., ranging from about 10-90 nm, 10-80 nm, 10-70 nm, 10-60 nm, or 10-50 nm). In a particular embodiment, a suitable liposome has a size less than about 100 nm.
A variety of alternative methods known in the art are available for sizing of a population of liposomes. One such sizing method is described in U.S. Pat. No. 4,737,323, incorporated herein by reference. Sonicating a liposome suspension either by bath or probe sonication produces a progressive size reduction down to small ULV less than about 0.05 microns in diameter. Homogenization is another method that relies on shearing energy to fragment large liposomes into smaller ones. In a typical homogenization procedure, MLV are recirculated through a standard emulsion homogenizer until selected liposome sizes, typically between about 0.1 and 0.5 microns, are observed. The size of the liposomes may be determined by quasi-electric light scattering (QELS) as described in Bloomfield, Ann. Rev. Biophys. Bioeng., 10:421-150 (1981), incorporated herein by reference. Average liposome diameter may be reduced by sonication of formed liposomes. Intermittent sonication cycles may be alternated with QELS assessment to guide efficient liposome synthesis.
Polymers
In some embodiments, a suitable delivery vehicle is formulated using a polymer as a carrier, alone or in combination with other carriers including various lipids described herein. Thus, in some embodiments, liposomal delivery vehicles, as used herein, also encompass polymer containing nanoparticles. Suitable polymers may include, for example, polyacrylates, polyalkycyanoacrylates, polylactide, polylactide-polyglycolide copolymers, polycaprolactones, dextran, albumin, gelatin, alginate, collagen, chitosan, cyclodextrins, protamine, PEGylated protamine, PLL, PEGylated PLL and polyethylenimine (PEI). When PEI is present, it may be branched PEI of a molecular weight ranging from 10 to 40 kDa, e.g., 25 kDa branched PEI (Sigma #408727).
A suitable liposome for the present invention may include one or more of any of the cationic lipids, non-cationic lipids, cholesterol lipids, PEGylated lipids and/or polymers described herein at various ratios. As non-limiting examples, a suitable liposome formulation may include a combination selected from cKK-E12, DOPE, cholesterol and DMG-PEG2K; C12-200, DOPE, cholesterol and DMG-PEG2K; HGT4003, DOPE, cholesterol and DMG-PEG2K; or ICE, DOPE, cholesterol and DMG-PEG2K.
In various embodiments, cationic lipids (e.g., cKK-E12, C12-200, ICE, and/or HGT4003) constitute about 30-60% (e.g., about 30-55%, about 30-50%, about 30-45%, about 30-40%, about 35-50%, about 35-45%, or about 35-40%) of the liposome by molar ratio. In some embodiments, the percentage of cationic lipids (e.g., cKK-E12, C12-200, ICE, and/or HGT4003) is or greater than about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, or about 60% of the liposome by molar ratio.
In some embodiments, the ratio of cationic lipid(s) to non-cationic lipid(s) to cholesterol-based lipid(s) to PEGylated lipid(s) may be between about 30-60:25-35:20-30:1-15, respectively. In some embodiments, the ratio of cationic lipid(s) to non-cationic lipid(s) to cholesterol-based lipid(s) to PEGylated lipid(s) is approximately 40:30:20:10, respectively. In some embodiments, the ratio of cationic lipid(s) to non-cationic lipid(s) to cholesterol-based lipid(s) to PEGylated lipid(s) is approximately 40:30:25:5, respectively. In some embodiments, the ratio of cationic lipid(s) to non-cationic lipid(s) to cholesterol-based lipid(s) to PEGylated lipid(s) is approximately 40:32:25:3, respectively. In some embodiments, the ratio of cationic lipid(s) to non-cationic lipid(s) to cholesterol-based lipid(s) to PEGylated lipid(s) is approximately 50:25:20:5.

Pharmaceutical Compositions

To facilitate expression of MCNA in vivo, delivery vehicles such as liposomes can be formulated in combination with one or more additional nucleic acids, carriers, targeting ligands or stabilizing reagents, or in pharmacological compositions where it is mixed with suitable excipients. Techniques for formulation and administration of drugs may be found in “Remington's Pharmaceutical Sciences,” Mack Publishing Co., Easton, Pa., latest edition.
In some embodiments, a composition comprises MCNA encapsulated or complexed with a delivery vehicle. In some embodiments, the delivery vehicle is selected from the group consisting of liposomes, lipid nanoparticles, solid-lipid nanoparticles, polymers, viruses, sol-gels, and nanogels.
Provided liposomally-encapsulated or liposomally-associated MCNA, and compositions containing the same, may be administered and dosed in accordance with current medical practice, taking into account the clinical condition of the subject, the site and method of administration, the scheduling of administration, the subject's age, sex, body weight and other factors relevant to clinicians of ordinary skill in the art. The “effective amount” for the purposes herein may be determined by such relevant considerations as are known to those of ordinary skill in experimental clinical research, pharmacological, clinical and medical arts. In some embodiments, the amount administered is effective to achieve at least some stabilization, improvement or elimination of symptoms and other indicators as are selected as appropriate measures of disease progress, regression or improvement by those of skill in the art. For example, a suitable amount and dosing regimen is one that causes at least transient protein (e.g., enzyme) production.
The present invention provides methods of delivering MCNA for in vivo protein production, comprising administering MCNA to a subject in need of delivery. In some embodiments, MCNA is administered via a route of delivery selected from the group consisting of intravenous delivery, subcutaneous delivery, oral delivery, subdermal delivery, ocular delivery, intratracheal injection pulmonary delivery (e.g. nebulization), intramuscular delivery, intrathecal delivery, or intraarticular delivery.
Suitable routes of administration include, for example, oral, rectal, vaginal, transmucosal, pulmonary including intratracheal or inhaled, or intestinal administration; parenteral delivery, including intradermal, transdermal (topical), intramuscular, subcutaneous, intramedullary injections, as well as intrathecal, direct intraventricular, intravenous, intraperitoneal, or intranasal. In particular embodiments, the intramuscular administration is to a muscle selected from the group consisting of skeletal muscle, smooth muscle and cardiac muscle. In some embodiments the administration results in delivery of the MCNA to a muscle cell. In some embodiments the administration results in delivery of the MCNA to a hepatocyte (i.e., liver cell). In a particular embodiment, the intramuscular administration results in delivery of the MCNA to a muscle cell.
Alternatively or additionally, liposomally-encapsulated MCNA and compositions of the invention may be administered in a local rather than systemic manner, for example, via injection of the pharmaceutical composition directly into a targeted tissue, preferably in a sustained release formulation. Local delivery can be affected in various ways, depending on the tissue to be targeted. For example, aerosols containing compositions of the present invention can be inhaled (for nasal, tracheal, or bronchial delivery); compositions of the present invention can be injected into the site of injury, disease manifestation, or pain, for example; compositions can be provided in lozenges for oral, tracheal, or esophageal application; can be supplied in liquid, tablet or capsule form for administration to the stomach or intestines, can be supplied in suppository form for rectal or vaginal application; or can even be delivered to the eye by use of creams, drops, or even injection. Formulations containing provided compositions complexed with therapeutic molecules or ligands can even be surgically administered, for example in association with a polymer or other structure or substance that can allow the compositions to diffuse from the site of implantation to surrounding cells. Alternatively, they can be applied surgically without the use of polymers or supports.
Provided methods of the present invention contemplate single as well as multiple administrations of a therapeutically effective amount of the therapeutic agents (e.g., MCNA) described herein. Therapeutic agents can be administered at regular intervals, depending on the nature, severity and extent of the subject's condition. In some embodiments, a therapeutically effective amount of the therapeutic agents (e.g., MCNA) of the present invention may be administered intrathecally periodically at regular intervals (e.g., once every year, once every six months, once every five months, once every three months, bimonthly (once every two months), monthly (once every month), biweekly (once every two weeks), twice a month, once every 30 days, once every 28 days, once every 14 days, once every 10 days, once every 7 days, weekly, twice a week, daily or continuously).
In some embodiments, provided liposomes and/or compositions are formulated such that they are suitable for extended-release of the MCNA contained therein. Such extended-release compositions may be conveniently administered to a subject at extended dosing intervals. For example, in one embodiment, the compositions of the present invention are administered to a subject twice a day, daily or every other day. In a preferred embodiment, the compositions of the present invention are administered to a subject twice a week, once a week, once every 7 days, once every 10 days, once every 14 days, once every 28 days, once every 30 days, once every two weeks, once every three weeks, or more preferably once every four weeks, once a month, twice a month, once every six weeks, once every eight weeks, once every other month, once every three months, once every four months, once every six months, once every eight months, once every nine months or annually. Also contemplated are compositions and liposomes which are formulated for depot administration (e.g., intramuscularly, subcutaneously, intravitreally) to either deliver or release MCNA over extended periods of time. Preferably, the extended-release means employed are combined with modifications made to the MCNA to enhance stability.
As used herein, the term “therapeutically effective amount” is largely determined based on the total amount of the therapeutic agent contained in the pharmaceutical compositions of the present invention. Generally, a therapeutically effective amount is sufficient to achieve a meaningful benefit to the subject (e.g., treating, modulating, curing, preventing and/or ameliorating a disease or disorder). For example, a therapeutically effective amount may be an amount sufficient to achieve a desired therapeutic and/or prophylactic effect. Generally, the amount of a therapeutic agent (e.g., MCNA) administered to a subject in need thereof will depend upon the characteristics of the subject. Such characteristics include the condition, disease severity, general health, age, sex and body weight of the subject. One of ordinary skill in the art will be readily able to determine appropriate dosages depending on these and other related factors. In addition, both objective and subjective assays may optionally be employed to identify optimal dosage ranges.
A therapeutically effective amount is commonly administered in a dosing regimen that may comprise multiple unit doses. For any particular therapeutic protein, a therapeutically effective amount (and/or an appropriate unit dose within an effective dosing regimen) may vary, for example, depending on route of administration, on combination with other pharmaceutical agents. Also, the specific therapeutically effective amount (and/or unit dose) for any particular patient may depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific pharmaceutical agent employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and/or rate of excretion or metabolism of the specific protein employed; the duration of the treatment; and like factors as is well known in the medical arts.
In some embodiments, the therapeutically effective dose ranges from about 0.005 mg/kg body weight to 500 mg/kg body weight, e.g., from about 0.005 mg/kg body weight to 400 mg/kg body weight, from about 0.005 mg/kg body weight to 300 mg/kg body weight, from about 0.005 mg/kg body weight to 200 mg/kg body weight, from about 0.005 mg/kg body weight to 100 mg/kg body weight, from about 0.005 mg/kg body weight to 90 mg/kg body weight, from about 0.005 mg/kg body weight to 80 mg/kg body weight, from about 0.005 mg/kg body weight to 70 mg/kg body weight, from about 0.005 mg/kg body weight to 60 mg/kg body weight, from about 0.005 mg/kg body weight to 50 mg/kg body weight, from about 0.005 mg/kg body weight to 40 mg/kg body weight, from about 0.005 mg/kg body weight to 30 mg/kg body weight, from about 0.005 mg/kg body weight to 25 mg/kg body weight, from about 0.005 mg/kg body weight to 20 mg/kg body weight, from about 0.005 mg/kg body weight to 15 mg/kg body weight, from about 0.005 mg/kg body weight to 10 mg/kg body weight.
In some embodiments, the therapeutically effective dose is greater than about 0.1 mg/kg body weight, greater than about 0.5 mg/kg body weight, greater than about 1.0 mg/kg body weight, greater than about 3 mg/kg body weight, greater than about 5 mg/kg body weight, greater than about 10 mg/kg body weight, greater than about 15 mg/kg body weight, greater than about 20 mg/kg body weight, greater than about 30 mg/kg body weight, greater than about 40 mg/kg body weight, greater than about 50 mg/kg body weight, greater than about 60 mg/kg body weight, greater than about 70 mg/kg body weight, greater than about 80 mg/kg body weight, greater than about 90 mg/kg body weight, greater than about 100 mg/kg body weight, greater than about 150 mg/kg body weight, greater than about 200 mg/kg body weight, greater than about 250 mg/kg body weight, greater than about 300 mg/kg body weight, greater than about 350 mg/kg body weight, greater than about 400 mg/kg body weight, greater than about 450 mg/kg body weight, greater than about 500 mg/kg body weight. In a particular embodiment, the therapeutically effective dose is 1.0 mg/kg. In some embodiments, the therapeutically effective dose of 1.0 mg/kg is administered intramuscularly or intravenously.
Also contemplated herein are lyophilized pharmaceutical compositions comprising one or more of the liposomes disclosed herein and related methods for the use of such compositions as disclosed for example, in U.S. Provisional Application No. 61/494,882, filed Jun. 8, 2011, the teachings of which are incorporated herein by reference in their entirety. For example, lyophilized pharmaceutical compositions according to the invention may be reconstituted prior to administration or can be reconstituted in vivo. For example, a lyophilized pharmaceutical composition can be formulated in an appropriate dosage form (e.g., an intradermal dosage form such as a disk, rod or membrane) and administered such that the dosage form is rehydrated over time in vivo by the individual's bodily fluids.
Provided liposomes and compositions may be administered to any desired tissue. In some embodiments, the MCNA delivered by provided liposomes or compositions is expressed in the tissue in which the liposomes and/or compositions were administered. In some embodiments, the MCNA delivered is expressed in a tissue different from the tissue in which the liposomes and/or compositions were administered. Exemplary tissues in which delivered MCNA may be delivered and/or expressed include, but are not limited to the liver, kidney, heart, spleen, serum, brain, skeletal muscle, lymph nodes, skin, and/or cerebrospinal fluid.
In some embodiments, administering the provided composition results in an increased MCNA expression level in a biological sample from a subject as compared to a baseline expression level before treatment. Typically, the baseline level is measured immediately before treatment. Biological samples include, for example, whole blood, serum, plasma, urine and tissue samples (e.g., muscle, liver, skin fibroblasts). In some embodiments, administering the provided composition results in an increased MCNA expression level by at least about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 95% as compared to the baseline level immediately before treatment. In some embodiments, administering the provided composition results in an increased MCNA expression level as compared to a MCNA expression level in subjects who are not treated
According to various embodiments, the timing of expression of delivered MCNA can be tuned to suit a particular medical need. In some embodiments, the expression of the protein encoded by delivered MCNA is detectable 1, 2, 3, 6, 12, 24, 48, 72, and/or 96 hours after administration of provided liposomes and/or compositions. In some embodiments, the expression of the protein encoded by delivered MCNA is detectable 1 week, two weeks, and/or 1 month after administration.

EXAMPLES

While certain compounds, compositions and methods of the present invention have been described with specificity in accordance with certain embodiments, the following examples serve only to illustrate the compounds of the invention and are not intended to limit the same.

Example 1. Exemplary Synthesis of Multimeric Coding Nucleic Acid (MCNA)

This example provides exemplary schemes for synthesizing the MCNA described in this application, for effective delivery and expression of MCNA encoding therapeutic proteins in vivo.
Synthesis of MCNA was attempted by ligating a synthetic oligonucleotide containing a 3′-3′ phosphodiester bond to multiple polynucleotides using a complementary DNA splint. Several different T4 RNA ligases were tested for the ability to ligate a synthetic oligonucleotide containing a 3′-3′ phosphodiester bond to multiple polynucleotides using a complementary DNA splint. The first RNA ligase (“RNA Ligase 1”) was a “single-strand” RNA ligase that ligated single RNA strands, double RNA strands and double RNA strands designed to implement a single strand overhang. The second RNA ligase (“RNA Ligase 2”) was a “double-stranded” RNA ligase that ligated nicks in RNA bound to a complementary oligonucleotide. Both RNA Ligase 1 and RNA Ligase 2 required phosphorylated 5′ ends of the oligonucleotide bridge to proceed with adenylation for the ligation reaction.
As a non-limiting example, Erythropoietin (EPO) mRNA was ligated to a bridging oligo containing a 3′-3′ phosphodiester bond using a complementary DNA splint. Examples of a bridging oligonucleotide that contains a 3′-3′ phosphodiester bond and DNA splints are described below. The exemplary sequence for EPO used in the examples herein are listed below.

Erythropoietin (EPO) mRNA (including 5′ and 3′ UTR):
(SEQ ID NO: 1)
GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGACACC

GGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGGAUUCCCCG

UGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACGAAUGUCCUGCCU

GGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGGGCCUCCCAGUCCUGGG

CGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCCUGGAGAGGUACCUCUUGGAG

GCCAAGGAGGCCGAGAAUAUCACGACGGGCUGUGCUGAACACUGCAGCUUGAAU

GAGAAUAUCACUGUCCCAGACACCAAAGUUAAUUUCUAUGCCUGGAAGAGGAUG

GAGGUCGGGCAGCAGGCCGUAGAAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAG

CUGUCCUGCGGGGCCAGGCCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCU

GCAGCUGCAUGUGGAUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUU

CGGGCUCUGGGAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUG

CUCCACUCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUC

CAAUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGG

GGACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCCCU

GGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGUUGCAUC

AAGCU

Erythropoietin (EPO) mRNA (including 5′ and 3′ UTR with
200 A poly(A) Tail):
(SEQ ID NO: 2)
GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGACACC

GGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGGAUUCCCCG

UGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACGAAUGUCCUGCCU

GGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGGGCCUCCCAGUCCUGGG

CGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCCUGGAGAGGUACCUCUUGGAG

GCCAAGGAGGCCGAGAAUAUCACGACGGGCUGUGCUGAACACUGCAGCUUGAAU

GAGAAUAUCACUGUCCCAGACACCAAAGUUAAUUUCUAUGCCUGGAAGAGGAUG

GAGGUCGGGCAGCAGGCCGUAGAAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAG

CUGUCCUGCGGGGCCAGGCCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCU

GCAGCUGCAUGUGGAUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUU

CGGGCUCUGGGAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUG

CUCCACUCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUC

CAAUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGG

GGACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCCCU

GGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGUUGCAUC

AAGCUAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Erythropoietin (EPO) mRNA (including 5′ and 3′ UTR with
internal 65A poly(A) region in 3′ UTR):
(SEQ ID NO: 3)
GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGACACC

GGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGGAUUCCCCG

UGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACGAAUGUCCUGCCU

GGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGGGCCUCCCAGUCCUGGG

CGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCCUGGAGAGGUACCUCUUGGAG

GCCAAGGAGGCCGAGAAUAUCACGACGGGCUGUGCUGAACACUGCAGCUUGAAU

GAGAAUAUCACUGUCCCAGACACCAAAGUUAAUUUCUAUGCCUGGAAGAGGAUG

GAGGUCGGGCAGCAGGCCGUAGAAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAG

CUGUCCUGCGGGGCCAGGCCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCU

GCAGCUGCAUGUGGAUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUU

CGGGCUCUGGGAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUG

CUCCACUCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUC

CAAUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGG

GGACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCCCU

GGAAGUUGCCACUCCAGUGCCCACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCUUGUCCUAAUAAAAU

UAAGUUGCAUCAAGCU

Erythropoietin (EPO) mRNA (including 5′ and 3′ UTR with
multiple short internal poly(A) regions in 3′ UTR):
(SEQ ID NO: 4)
GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGACACC

GGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGGAUUCCCCG

UGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACGAAUGUCCUGCCU

GGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGGGCCUCCCAGUCCUGGG

CGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCCUGGAGAGGUACCUCUUGGAG

GCCAAGGAGGCCGAGAAUAUCACGACGGGCUGUGCUGAACACUGCAGCUUGAAU

GAGAAUAUCACUGUCCCAGACACCAAAGUUAAUUUCUAUGCCUGGAAGAGGAUG

GAGGUCGGGCAGCAGGCCGUAGAAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAG

CUGUCCUGCGGGGCCAGGCCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCU

GCAGCUGCAUGUGGAUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUU

CGGGCUCUGGGAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUG

CUCCACUCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUC

CAAUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGG

GGACAGAUGACGGGUGGCAAAAAAAAAAAAAAAUCCCUGUGACCCCUCCCCAAAA

AAAAAAAAAAAAGUGCCUCUCCUGGCCCUGGAAAAAAAAAAAAAAAGUUGCCAC

UCCAGUGCCCACCAAAAAAAAAAAAAAAGCCUUGUCCUAAUAAAAUUAAGUUGC

AUCAAGCU

Bridging Oligonucleotide 1:
(SEQ ID NO: 5)
5′-CGA CUC UCG G-3′-PO₄-3′-G GCU CUC AGC-5′
The bases included in SEQ ID NO: 5 are 2′-O-methyl RNA
and the 3′-3′ bridge comprises PO_4.

Bridging Oligonucleotide 2:
(SEQ ID NO: 6)
5′-AAAAAAAAAA-3′-PO ₄ -3′-AAAAAAAAAA-5′

Bridging Oligonucleotide 3:
(SEQ ID NO: 7)
5′-AAA-3′-PO ₄ -3′-AAA-5′

Bridging Oligonucleotide 4:
(SEQ ID NO: 8)
5′-A-3′-PO ₄ -3′-A-5′

Splint Oligonucleotide 1:
(SEQ ID NO: 9)
5′-CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G-3′

Splint Oligonucleotide 2:
(SEQ ID NO: 10)
5′-CCG AGA GTG ATG CAA CTT AAT TTT ATT AGG-3′

Splint Oligonucleotide 3:
(SEQ ID NO: 11)
5′-TTT TTT TTT TAG CTT GAT GCA ACT TAA TTT TAT TAG G-3′

Splint Oligonucleotide 4:
(SEQ ID NO: 12)
5′-CCG AGA GTC GTT TTT TTT TTT TTT TTT TTT-3′

Splint Oligonucleotide 5:
(SEQ ID NO: 13)
3′-G GAT TAT TTT AAT TCA ACG TAG TTC GAG CTG AGA GCC-5′-PO₄-5′-CCG AGA

GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G-3′

Splint Oligonucleotide 6:
(SEQ ID NO: 14)
3′-GGA TTA TTT TAA TTC AAC GTA GTG AGA GCC-5′-PO₄-5′-CCG AGA GTG ATG

CAA CTT AAT TTT ATT AGG-3′

Splint Oligonucleotide 7:
(SEQ ID NO: 15)
3′-G GAT TAT TTT AAT TCA ACG TAG TTC GAT TTT TTT TTT-5′-PO₄-5′-TTT TTT TTT

TAG CTT GAT GCA ACT TAA TTT TAT TAG G-3′

Splint Oligonucleotide 8:
(SEQ ID NO: 16)
3′-TTT TTT TTT TTT TTT TTT TTG CTG AGA GCC-5′-PO₄-5′-CCG AGA GTC GTT TTT

TTT TTT TTT TTT TTT-3′

EPO MCNA #1 (No Poly a Tail)
MCNA 1 (SEQ ID NO: 17) was prepared by splint ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′ untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure, and purified. This hEPO transcript was then ligated in a single step to a 2′-hydroxymethylated RNA (OMeRNA) “bridging” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(bridging oligo 1; 5′- CGA CUC UCGG -3′-3′- G GCU CUC

AGC -5′, bold bases OMeRNA)

using either (A) T4 RNA ligase 1+PEG 8K, (B) T4 RNA ligase 1 or (C) T4 RNA Ligase 2 and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo 1 (splint oligo 1 (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). Alternatively, MCNA was prepared using splint oligonucleotide 5 (SEQ ID NO: 13), a palindromic sequence containing 2 copies of oligo 2 connected with a 5′-5′ phosphodiester bond. To prepare the samples for ligation, bridging oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM bridging oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 h. Phosphorylated bridging oligo 1 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 1 and 3 μM splint oligo 1 (or 1.5 uM splint oligo 5) by heating to 75° C. for 5 min followed by gradual cooling to room temperature over 5 min. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and (A) 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP and 1 U/μL T4 RNA ligase 1 (NEB), (B) 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB) or (C) 1×T4RNA Ligase 2 Buffer (NEB; 50 mM Tris-HCl, 2 mM MgCl₂, 1 mM DTT, 400 μM ATP at pH 7.5 at 25° C.) and 1 U/μL T4 RNA ligase 2 (NEB). Each was reacted for 90 minutes at 37° C. The completed ligation reaction was then purified using an RNeasy Mini Kit (Qiagen). A portion of the purified MCNA 1 product was subsequently treated with DNase I to remove residual bridge oligonucleotide to prevent potential endogenous RNase H cleavage of PCNA 1 in cells.
Alternatively, MCNA 1 (SEQ ID NO: 17) was prepared by splint ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hEPO transcript was then ligated in a single step to a 2′-hydroxymethylated RNA (OMeRNA) “bridging” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(bridging oligo 1; 5′- CGA CUC UCG G -3′-3′- G GCU CUC

AGC -5′, bold bases OMeRNA)

using either (A) T4 RNA ligase 1+PEG 8K, (B) T4 RNA ligase 1 or (C) T4 RNA Ligase 2 and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo 1 (splint oligo 1 (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). Alternatively, MCNA was prepared using splint oligonucleotide 6 (SEQ ID NO: 14), and a palindromic sequence containing 2 copies of oligo 2 connected with a 5′-5′ phosphodiester bond. To prepare the samples for ligation, bridging oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM bridging oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 1 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 1 and 3 μM splint oligo 1 (or 1.5 uM splint oligo 6) by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and (A) 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP and 1 U/μL T4 RNA ligase 1 (NEB), (B) 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB) or (C) 1×T4RNA Ligase 2 Buffer (NEB; 50 mM Tris-HCl, 2 mM MgCl₂, 1 mM DTT, 400 μM ATP pH 7.5 at 25° C.) and 1 U/μL T4 RNA ligase 2 (NEB). Each was reacted for 90 minutes 37° C. The completed ligation reaction was then purified using an RNeasy Mini Kit (Qiagen). A portion of the purified MCNA 1 product was subsequently treated with DNase I to remove residual bridge oligonucleotide to prevent potential endogenous RNase H cleavage of PCNA 1 in cells.
MCNA 1 (No Poly(A) Tail Sequence):

(SEQ ID NO: 17)

5′-

GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGA

CACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGG

AUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACG

AAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGG

GCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCC

UGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGGGCU

GUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCAAAG

UUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAGAAG

UCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGGCCC

UGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGGAUA

AAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGGGAG

CCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCACUCC

GAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCAAUU

UCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGGGG

ACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCC

CUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGU

UGCAUCAAGCU

UCGAACUA

CGUUGAAUUAAAAUAAUCCUGUUCCGACCACCCGUGACCUCACCGUUGAAG

GUCCCGGUCCUCUCCGUGACCCCUCCCCAGUGUCCCUACGGUGGGCAGUAG

ACAGGGGACAGGACGUCCGGAGGGGACACAUGUCGAAGUCGAAAGGGGCCU

CCUUUAACCUCAUCUGAGCCUUCUCAAACGCCUUUCACAGUCGUCACUAAC

AAGCCUCACCUCGUCGACUCCGGCGUAGACCUCCCCUCUACCGAAGGAAGA

CCCGAGGGUCUCGGGCUUCGUCUCACCACUCCGACGCUUCCGGUGACUGCC

GAAAUAGGUGUACGUCGACGUCCCCGAGGGUGCCGACCCUUCUCAACUGGU

UGUCCCGGACCGGGGCGUCCUGUCGAAGGCUGUCGUCCCGGUCCGGGACGG

UCUGAAGAUGCCGGACGACGGGCUGGAGGUAGGAGAAGGUCCGUAUCUUUA

AUUGAAACCACAGACCCUGUCACUAUAAGAGUAAGUUCGACGUCACAAGUC

GUGUCGGGCAGCACUAUAAGAGCCGGAGGAACCGGAGGUUCUCCAUGGAGA

GGUCCUGAGCCGACAGUGUCUACUCCGCACCACCCCGCGGGUCCUGACCCU

CCGGGUCUCCCUCGCUGUCGUCCCUGUCCUCUUCGGUGUCGGUCCGUCCUG

UAAGCACGUGGGGGUAGCACAGUUCCUGCCACUCAGUGAGAACCGUGCCCC

UUAGGCGCAAGGUUACGUGGCAAGGGCCGGCGCCUCCGACCUAGCCAGGGC

CACAGAAGAUACCUCCAGUUUUGUCGCACCUACCGCAGAGGUCCGCUAGAC

AGG-5′

EPO MCNA #2
MCNA 2 (SEQ ID NO: 18) was prepared by splint ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hEPO transcript was then ligated in a single step to an RNA “bridging” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10th and 11^thnt
(SEQ ID NO: 6)

(bridging oligo 2; 5′-AAA AAA AAA A-3′-3′-A AAA

AAA AAA-5′, underlined bases RNA)

using T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo 2 (splint oligo 3 (SEQ ID NO: 11); 5′ TTT TTT TTT TAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). Alternatively, MCNA was prepared using splint oligo 7 (SEQ ID NO: 15), a palindromic sequence containing 2 copies of splint oligo 7 connected with a 5′-5′ phosphodiester bond. To prepare the samples for ligation, bridging oligo 2 was 5′-end phosphorylated in a reaction containing 50 μM oligo 3, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT, pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 2 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 2 and 3 μM splint oligo 3 (or 1.5 uM splint oligo 7) by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and was reacted for 90 min at 37° C. The completed ligation reaction was then purified using an RNeasy Mini Kit (Qiagen).

EPO PCNA #2 (10A-10A Bridge):

(SEQ ID NO: 18)

5′-

GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGA

CACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGG

AUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACG

AAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGG

GCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCC

UGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGGGCU

GUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCAAAG

UUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAGAAG

UCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGGCCC

UGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGGAUA

AAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGGGAG

CCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCACUCC

GAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCAAUU

UCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGGGG

ACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCC

CUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGU

UGCAUCAAGCU AAAAAAAAAA-

AAAAAAAAAA UCGAACUA

CGUUGAAUUAAAAUAAUCCUGUUCCGACCACCCGUGACCUCACCGUUGAAG

GUCCCGGUCCUCUCCGUGACCCCUCCCCAGUGUCCCUACGGUGGGCAGUAG

ACAGGGGACAGGACGUCCGGAGGGGACACAUGUCGAAGUCGAAAGGGGCCU

CCUUUAACCUCAUCUGAGCCUUCUCAAACGCCUUUCACAGUCGUCACUAAC

AAGCCUCACCUCGUCGACUCCGGCGUAGACCUCCCCUCUACCGAAGGAAGA

CCCGAGGGUCUCGGGCUUCGUCUCACCACUCCGACGCUUCCGGUGACUGCC

GAAAUAGGUGUACGUCGACGUCCCCGAGGGUGCCGACCCUUCUCAACUGGU

UGUCCCGGACCGGGGCGUCCUGUCGAAGGCUGUCGUCCCGGUCCGGGACGG

UCUGAAGAUGCCGGACGACGGGCUGGAGGUAGGAGAAGGUCCGUAUCUUUA

AUUGAAACCACAGACCCUGUCACUAUAAGAGUAAGUUCGACGUCACAAGUC

GUGUCGGGCAGCACUAUAAGAGCCGGAGGAACCGGAGGUUCUCCAUGGAGA

GGUCCUGAGCCGACAGUGUCUACUCCGCACCACCCCGCGGGUCCUGACCCU

CCGGGUCUCCCUCGCUGUCGUCCCUGUCCUCUUCGGUGUCGGUCCGUCCUG

UAAGCACGUGGGGGUAGCACAGUUCCUGCCACUCAGUGAGAACCGUGCCCC

UUAGGCGCAAGGUUACGUGGCAAGGGCCGGCGCCUCCGACCUAGCCAGGGC

CACAGAAGAUACCUCCAGUUUUGUCGCACCUACCGCAGAGGUCCGCUAGAC

AGG-5′

EPO MCNA #3
MCNA 3 (SEQ ID NO: 19) was prepared by splint ligation of the 3′end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′ untranslated region (UTR), a 3′ UTR with both UTRs flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. The construct was treated further to incorporate a poly(A) tail length of ˜200 As using poly(A) polymerase. This hEPO transcript was then ligated in a single step to OMeRNA “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(bridging oligo 1; 5′- CGA CUC UCG G -3′-3′- G GCU

CUC AGC -5′, bold bases OMeRNA)

using T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo 1 (splint oligo 4 (SEQ ID NO: 12); 5′ CCG AGA GTC GTT TTT TTT TTT TTT TTT TTT 3′; all bases DNA). Alternatively, MCNA could be prepared using splint oligo 8 (SEQ ID NO: 16), a palindromic sequence containing 2 copies of splint oligo 4 connected with a 5′-5′ phosphodiester bond. To prepare the samples for ligation, bridging oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT, pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 1 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 1 and 3 μM splint oligo 4 by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and was reacted for 90 minutes at 37° C. The completed ligation reaction was then purified using an RNeasy Mini Kit (Qiagen).

EPO PCNA #3 (Includes 200A Poly(A) Tail):

(SEQ ID NO: 19)

5′-

GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGA

CACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGG

AUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACG

AAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGG

GCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCC

UGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGGGCU

GUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCAAAG

UUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAGAAG

UCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGGCCC

UGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGGAUA

AAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGGGAG

CCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCACUCC

GAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCAAUU

UCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGGGG

ACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCC

CUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGU

UGCAUCAAGCUAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAA-

AAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAUCGAACUACGUUGA

AUUAAAAUAAUCCUGUUCCGACCACCCGUGACCUCACCGUUGAAGGUCCCG

GUCCUCUCCGUGACCCCUCCCCAGUGUCCCUACGGUGGGCAGUAGACAGGG

GACAGGACGUCCGGAGGGGACACAUGUCGAAGUCGAAAGGGGCCUCCUUUA

ACCUCAUCUGAGCCUUCUCAAACGCCUUUCACAGUCGUCACUAACAAGCCU

CACCUCGUCGACUCCGGCGUAGACCUCCCCUCUACCGAAGGAAGACCCGAG

GGUCUCGGGCUUCGUCUCACCACUCCGACGCUUCCGGUGACUGCCGAAAUA

GGUGUACGUCGACGUCCCCGAGGGUGCCGACCCUUCUCAACUGGUUGUCCC

GGACCGGGGCGUCCUGUCGAAGGCUGUCGUCCCGGUCCGGGACGGUCUGAA

GAUGCCGGACGACGGGCUGGAGGUAGGAGAAGGUCCGUAUCUUUAAUUGAA

ACCACAGACCCUGUCACUAUAAGAGUAAGUUCGACGUCACAAGUCGUGUCG

GGCAGCACUAUAAGAGCCGGAGGAACCGGAGGUUCUCCAUGGAGAGGUCCU

GAGCCGACAGUGUCUACUCCGCACCACCCCGCGGGUCCUGACCCUCCGGGU

CUCCCUCGCUGUCGUCCCUGUCCUCUUCGGUGUCGGUCCGUCCUGUAAGCA

CGUGGGGGUAGCACAGUUCCUGCCACUCAGUGAGAACCGUGCCCCUUAGGC

GCAAGGUUACGUGGCAAGGGCCGGCGCCUCCGACCUAGCCAGGGCCACAGA

AGAUACCUCCAGUUUUGUCGCACCUACCGCAGAGGUCCGCUAGACAGG-5′

EPO MCNA #4
MCNA 4 (SEQ ID NO: 20) was prepared by splint-independent ligation of the 3′-end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′-ends of a single dinucleotide containing two A's linked by a 3′-3′ phosphodiester bond. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR), a 3′ UTR with both UTRs flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. The construct was treated further to incorporate a poly(A) tail length of ˜200 As using poly(A) polymerase. This hEPO transcript was then ligated via two steps to an RNA bridge oligonucleotide containing a trimeric repeat of As with a 3′-3′ phosphodiester linkage to another trimeric repeat of As (bridging oligo 3 (SEQ ID NO: 7); 5′-AAA-3′-3′-AAA-5′, underlined bases RNA) using T4 RNA ligase 1+PEG 8K. To prepare the samples for ligation, bridging oligo 3 was 5′-end phosphorylated in a reaction containing 50 μM oligo 7, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT, pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 3 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and denatured in a reaction containing 2.4 μM capped and tailed hEPO transcript and 50 μM bridging oligo 3 by heating to 75° C. for 5 min followed by gradual cooling to room temperature over 5 min. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and was reacted for 90 minutes at 37° C. The partial ligation reaction was then purified using an RNeasy Mini Kit (Qiagen). The ligation reaction was repeated using a 1:1 molar ratio of the partial ligation product and additional capped and tailed hEPO transcript, and purified as previously.
EPO PCNA #4 (Includes 200A Poly(A) Tail with 3A-3A Bridge):

(SEQ ID NO: 20)

5′-

GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGAAGA

CACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACGCGG

AUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGCACG

AAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUCUGG

GCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAGUCC

UGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGGGCU

GUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCAAAG

UUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAGAAG

UCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGGCCC

UGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGGAUA

AAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGGGAG

CCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCACUCC

GAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCAAUU

UCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAGGGG

ACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCC

CUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGU

UGCAUCAAGCUAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAA- AAA

AAA-AAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAUCGAACUACGUUGAAUUAAAAUAAUCCUGU

UCCGACCACCCGUGACCUCACCGUUGAAGGUCCCGGUCCUCUCCGUGACCC

CUCCCCAGUGUCCCUACGGUGGGCAGUAGACAGGGGACAGGACGUCCGGAG

GGGACACAUGUCGAAGUCGAAAGGGGCCUCCUUUAACCUCAUCUGAGCCUU

CUCAAACGCCUUUCACAGUCGUCACUAACAAGCCUCACCUCGUCGACUCCG

GCGUAGACCUCCCCUCUACCGAAGGAAGACCCGAGGGUCUCGGGCUUCGUC

UCACCACUCCGACGCUUCCGGUGACUGCCGAAAUAGGUGUACGUCGACGUC

CCCGAGGGUGCCGACCCUUCUCAACUGGUUGUCCCGGACCGGGGCGUCCUG

UCGAAGGCUGUCGUCCCGGUCCGGGACGGUCUGAAGAUGCCGGACGACGGG

CUGGAGGUAGGAGAAGGUCCGUAUCUUUAAUUGAAACCACAGACCCUGUCA

CUAUAAGAGUAAGUUCGACGUCACAAGUCGUGUCGGGCAGCACUAUAAGAG

CCGGAGGAACCGGAGGUUCUCCAUGGAGAGGUCCUGAGCCGACAGUGUCUA

CUCCGCACCACCCCGCGGGUCCUGACCCUCCGGGUCUCCCUCGCUGUCGUC

CCUGUCCUCUUCGGUGUCGGUCCGUCCUGUAAGCACGUGGGGGUAGCACAG

UUCCUGCCACUCAGUGAGAACCGUGCCCCUUAGGCGCAAGGUUACGUGGCA

AGGGCCGGCGCCUCCGACCUAGCCAGGGCCACAGAAGAUACCUCCAGUUUU

GUCGCACCUACCGCAGAGGUCCGCUAGACAGG-5′

EPO MCNA #5
MCNA 5 (SEQ ID NO: 21) was prepared by splint-independent ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single dinucleotide containing two A's linked by a 3′-3′ phosphodiester bond. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR), a 3′ UTR with both UTRs flanking an RNA sequence encoding hEPO was transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. The construct was treated further to incorporate a poly(A) tail length of ˜200 As using poly(A) polymerase. This hEPO transcript was then ligated via two steps to an RNA “bridging” dinucleotide containing an A with a 3′-3′ phosphodiester linkage to another A (bridging oligo 4 (SEQ ID NO: 8); 5′ A 3′ 3′ A 5′, underlined bases RNA) using T4 RNA ligase 1+PEG 8K. To prepare the samples for ligation, bridging oligo 4 was 5′-end phosphorylated in a reaction containing 50 μM bridging oligo 4, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT, pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 4 was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and denatured in a reaction containing 2.4 μM capped and tailed hEPO transcript and 50 μM bridging oligo 4 by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and was reacted for 90 minutes at 37° C. The partial ligation reaction was then purified using an RNeasy Mini Kit (Qiagen). The ligation reaction was repeated using a 1:1 molar ratio of the partial ligation product and additional capped and tailed hEPO transcript, and purified as previously.
EPO PCNA #5 (Includes 200A Poly(A) Tail with 1A-1A Bridge):

(SEQ ID NO: 21)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGC

ACGAAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUC

UGGGCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAG

UCCUGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGG

GCUGUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCA

AAGUUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAG

AAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGG

CCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGG

AUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGG

GAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCAC

UCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCA

AUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAG

GGGACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUG

GCCCUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUA

AGUUGCAUCAAGCUAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAA-A-

-A-AAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAUCGAACUACGUUGAAUUAAAAUAAUCCUGUU

CCGACCACCCGUGACCUCACCGUUGAAGGUCCCGGUCCUCUCCGUGACCCC

UCCCCAGUGUCCCUACGGUGGGCAGUAGACAGGGGACAGGACGUCCGGAGG

GGACACAUGUCGAAGUCGAAAGGGGCCUCCUUUAACCUCAUCUGAGCCUUC

UCAAACGCCUUUCACAGUCGUCACUAACAAGCCUCACCUCGUCGACUCCGG

CGUAGACCUCCCCUCUACCGAAGGAAGACCCGAGGGUCUCGGGCUUCGUCU

CACCACUCCGACGCUUCCGGUGACUGCCGAAAUAGGUGUACGUCGACGUCC

CCGAGGGUGCCGACCCUUCUCAACUGGUUGUCCCGGACCGGGGCGUCCUGU

CGAAGGCUGUCGUCCCGGUCCGGGACGGUCUGAAGAUGCCGGACGACGGGC

UGGAGGUAGGAGAAGGUCCGUAUCUUUAAUUGAAACCACAGACCCUGUCAC

UAUAAGAGUAAGUUCGACGUCACAAGUCGUGUCGGGCAGCACUAUAAGAGC

CGGAGGAACCGGAGGUUCUCCAUGGAGAGGUCCUGAGCCGACAGUGUCUAC

UCCGCACCACCCCGCGGGUCCUGACCCUCCGGGUCUCCCUCGCUGUCGUCC

CUGUCCUCUUCGGUGUCGGUCCGUCCUGUAAGCACGUGGGGGUAGCACAGU

UCCUGCCACUCAGUGAGAACCGUGCCCCUUAGGCGCAAGGUUACGUGGCAA

GGGCCGGCGCCUCCGACCUAGCCAGGGCCACAGAAGAUACCUCCAGUUUUG

UCGCACCUACCGCAGAGGUCCGCUAGACAGG-5'

EPO PCNA #6
PCNA 6 (SEQ ID NO: 22) is prepared by splint ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR), a 3′ UTR containing an internal section of 65 consecutive As with both UTRs flanking an RNA sequence encoding hEPO is transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hEPO transcript is then ligated in a single step to a OMeRNA “bridging” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(bridging oligo 1; 5'-CGA CUC UCG G-3'-3'-G GCU

CUC AGC-5', underlined bases OMeRNA)

using T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′ UTR and bridging oligo 1 (splint oligo 1 (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). To prepare the samples for ligation, bridging oligo 1 is 5′-end phosphorylated in a reaction containing 50 μM bridging oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 1 is then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 1 and 3 μM splint oligo 1 by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction is subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and is reacted for 90 minutes at 37° C. The completed ligation reaction is then purified using an RNeasy Mini Kit (Qiagen).

EPO PCNA #6 (Includes Internal 65A Poly(A) Region):

(SEQ ID NO: 22)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGC

ACGAAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUC

UGGGCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAG

UCCUGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGG

GCUGUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCA

AAGUUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAG

AAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGG

CCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGG

AUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGG

GAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCAC

UCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCA

AUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAG

GGGACAGAUGACGGGUGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUG

GCCCUGGAAGUUGCCACUCCAGUGCCCACCAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCUUGU

CCUAAUAAAAUUAAGUUGCAUCAAGCU CGACUCUCGG-

-GGCU

CUCAGC UCGAACUACGUUGAAUUAAAAUAAUCCUGUUCCGAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAACCACCCGUGACCUCACCGUUGAAGGUCCCGGUCCUCUCCGUGACCCCU

CCCCAGUGUCCCUACGGUGGGCAGUAGACAGGGGACAGGACGUCCGGAGGG

GACACAUGUCGAAGUCGAAAGGGGCCUCCUUUAACCUCAUCUGAGCCUUCU

CAAACGCCUUUCACAGUCGUCACUAACAAGCCUCACCUCGUCGACUCCGGC

GUAGACCUCCCCUCUACCGAAGGAAGACCCGAGGGUCUCGGGCUUCGUCUC

ACCACUCCGACGCUUCCGGUGACUGCCGAAAUAGGUGUACGUCGACGUCCC

CGAGGGUGCCGACCCUUCUCAACUGGUUGUCCCGGACCGGGGCGUCCUGUC

GAAGGCUGUCGUCCCGGUCCGGGACGGUCUGAAGAUGCCGGACGACGGGCU

GGAGGUAGGAGAAGGUCCGUAUCUUUAAUUGAAACCACAGACCCUGUCACU

AUAAGAGUAAGUUCGACGUCACAAGUCGUGUCGGGCAGCACUAUAAGAGCC

GGAGGAACCGGAGGUUCUCCAUGGAGAGGUCCUGAGCCGACAGUGUCUACU

CCGCACCACCCCGCGGGUCCUGACCCUCCGGGUCUCCCUCGCUGUCGUCCC

UGUCCUCUUCGGUGUCGGUCCGUCCUGUAAGCACGUGGGGGUAGCACAGUU

CCUGCCACUCAGUGAGAACCGUGCCCCUUAGGCGCAAGGUUACGUGGCAAG

GGCCGGCGCCUCCGACCUAGCCAGGGCCACAGAAGAUACCUCCAGUUUUGU

CGCACCUACCGCAGAGGUCCGCUAGACAGG-5'

EPO PCNA #7
PCNA7 (SEQ ID NO: 23) is prepared by splint ligation of the 3′ end of two copies of an RNA encoding the human Erythropoietin (hEPO) protein to the 5′ ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′ untranslated region (UTR), a 3′ UTR containing 3 stretches of 15 As and 1 stretch of 16 As with both UTRs flanking an RNA sequence encoding hEPO is transcribed using T7 RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hEPO transcript is then ligated in a single step to a OMeRNA “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(bridging oligo 1; 5'-CGA CUC UCG G-3'-3'-G GCU

CUC AGC-5', underlined bases OMeRNA)

using T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and bridging oligo 1 (splint oligo 1 (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). To prepare the samples for ligation, oligo 1 is 5′-end phosphorylated in a reaction containing 50 μM bridging oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT, pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated bridging oligo 1 is then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.2 μM capped hEPO transcript, 1.5 μM bridging oligo 1 and 3 μM splint oligo 1 by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction is subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 1 U/μL T4 RNA ligase 1 (NEB), and is reacted for 90 min at 37° C. The completed ligation reaction is then purified using an RNeasy Mini Kit (Qiagen).

EPO PCNA #7 (Includes Multiple Short Internal Poly(A) Regions):

(SEQ ID NO: 23)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGGGGGUGC

ACGAAUGUCCUGCCUGGCUGUGGCUUCUCCUGUCCCUGCUGUCGCUCCCUC

UGGGCCUCCCAGUCCUGGGCGCCCCACCACGCCUCAUCUGUGACAGCCGAG

UCCUGGAGAGGUACCUCUUGGAGGCCAAGGAGGCCGAGAAUAUCACGACGG

GCUGUGCUGAACACUGCAGCUUGAAUGAGAAUAUCACUGUCCCAGACACCA

AAGUUAAUUUCUAUGCCUGGAAGAGGAUGGAGGUCGGGCAGCAGGCCGUAG

AAGUCUGGCAGGGCCUGGCCCUGCUGUCGGAAGCUGUCCUGCGGGGCCAGG

CCCUGUUGGUCAACUCUUCCCAGCCGUGGGAGCCCCUGCAGCUGCAUGUGG

AUAAAGCCGUCAGUGGCCUUCGCAGCCUCACCACUCUGCUUCGGGCUCUGG

GAGCCCAGAAGGAAGCCAUCUCCCCUCCAGAUGCGGCCUCAGCUGCUCCAC

UCCGAACAAUCACUGCUGACACUUUCCGCAAACUCUUCCGAGUCUACUCCA

AUUUCCUCCGGGGAAAGCUGAAGCUGUACACAGGGGAGGCCUGCAGGACAG

GGGACAGAUGACGGGUGGCAAAAAAAAAAAAAAAUCCCUGUGACCCCUCCC

CAAAAAAAAAAAAAAAAGUGCCUCUCCUGGCCCUGGAAAAAAAAAAAAAAA

GUUGCCACUCCAGUGCCCACCAAAAAAAAAAAAAAAGCCUUGUCCUAAUAA

AAUUAAGUUGCAUCAAGCU CGACUCUCGG-

-GGCUCUCAGC UC

GAACUACGUUGAAUUAAAAUAAUCCUGUUCCGAAAAAAAAAAAAAAACCAC

CCGUGACCUCACCGUUGAAAAAAAAAAAAAAAGGUCCCGGUCCUCUCCGUG

AAAAAAAAAAAAAAAACCCCUCCCCAGUGUCCCUAAAAAAAAAAAAAAACG

GUGGGCAGUAGACAGGGGACAGGACGUCCGGAGGGGACACAUGUCGAAGUC

GAAAGGGGCCUCCUUUAACCUCAUCUGAGCCUUCUCAAACGCCUUUCACAG

UCGUCACUAACAAGCCUCACCUCGUCGACUCCGGCGUAGACCUCCCCUCUA

CCGAAGGAAGACCCGAGGGUCUCGGGCUUCGUCUCACCACUCCGACGCUUC

CGGUGACUGCCGAAAUAGGUGUACGUCGACGUCCCCGAGGGUGCCGACCCU

UCUCAACUGGUUGUCCCGGACCGGGGCGUCCUGUCGAAGGCUGUCGUCCCG

GUCCGGGACGGUCUGAAGAUGCCGGACGACGGGCUGGAGGUAGGAGAAGGU

CCGUAUCUUUAAUUGAAACCACAGACCCUGUCACUAUAAGAGUAAGUUCGA

CGUCACAAGUCGUGUCGGGCAGCACUAUAAGAGCCGGAGGAACCGGAGGUU

CUCCAUGGAGAGGUCCUGAGCCGACAGUGUCUACUCCGCACCACCCCGCGG

GUCCUGACCCUCCGGGUCUCCCUCGCUGUCGUCCCUGUCCUCUUCGGUGUC

GGUCCGUCCUGUAAGCACGUGGGGGUAGCACAGUUCCUGCCACUCAGUGAG

AACCGUGCCCCUUAGGCGCAAGGUUACGUGGCAAGGGCCGGCGCCUCCGAC

CUAGCCAGGGCCACAGAAGAUACCUCCAGUUUUGUCGCACCUACCGCAGAG

GUCCGCUAGACAGG-5'

FIG. 5 shows the results of MCNA detected via gel electrophoresis. MCNA run in lanes 1-15 were the result of a ligation reaction comprising an EPO mRNA to bridging oligonucleotide to DNA splint (SEQ ID NO: 9) molar ratio of 2:1:2. The molar amounts of EPO mRNA and RNA ligase are included in the below table:


Lane	EPO (μM)	Ligase (μM)

1	1.7	2.25 RNA Ligase 1
2	1.7	0.6 RNA Ligase 1
3	0.85	0.6 RNA Ligase 1
4	0.425	0.6 RNA Ligase 1
5	0.2125	0.6 RNA Ligase 1
6	1.7	2.25 RNA Ligase 1 + 10% PEG
7	1.7	0.6 RNA Ligase 1 + 10% PEG
8	0.85	0.6 RNA Ligase 1 + 10% PEG
9	0.425	0.6 RNA Ligase 1 + 10% PEG
10	0.2125	0.6 RNA Ligase 1 + 10% PEG
11	1.7	0.3 RNA Ligase 2
12	1.7	0.6 RNA Ligase 2
13	0.85	0.6 RNA Ligase 2
14	0.425	0.6 RNA Ligase 2
15	0.2125	0.6 RNA Ligase 2

FIG. 5 demonstrates that RNA Ligase 1 was superior to RNA Ligase 2 in producing MCNA comprising EPO RNA under the conditions tested. Further, the addition of 10% PEG to the reaction conditions enhanced ligation.

FIG. 6 shows MCNA detected via gel electrophoresis. Lane 1 shows Capped EPO mRNA (no poly(A) tail). Lane 2 shows a MCNA mixture of full length MCNA ligation product mixed with unreacted/partially reacted EPO RNA product (with no DNAse treatment). Lane 3 shows a MCNA mixture of full length MCNA ligation product mixed with unreacted/partially reacted EPO RNA product (with DNAse treatment).
FIG. 8 shows MCNA detected via gel electrophoresis. Lane 1 shows a RNA sizing ladder. Lane 2 shows a MCNA mixture of full length MCNA ligation product mixed with unreacted/partially reacted EPO RNA product. Lane 3 shows purified unreacted/partially reacted EPO RNA product. Lane 4 shows purified EPO MCNA ligation product.

MCNA-OTC Preparation

MCNA-OTC comprising human Ornithine Transcarbamylase (hOTC) RNA (SEQ ID NO: 24) was prepared by splint ligation of the 3′-end of two copies of an RNA encoding the hOTC protein to the 5′-ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hOTC was transcribed using RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hOTC transcript was then ligated in a single step to a 2′-hydroxymethylated RNA (OMeRNA) “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(oligo 1 (bridge); 5'- CGA CUC UCG G -3'-3'- G GCU

CUC AGC -5', bold bases OMeRNA)

using either T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and oligo 1 (oligo 2 (splint) (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). To prepare the samples for ligation, oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated oligo 1 (bridge) was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 3.3 μM capped hOTC transcript, 1.5 μM oligo 1 and 3.3 μM oligo 2 by heating to 75° C. for 5 minutes, followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 0.33 U/μL T4 RNA ligase 1. Each was reacted for 60 minutes at 37° C. The completed ligation reaction was then reacted with DNase I and subsequently purified using an RNeasy Maxi Kit (Qiagen). The reaction products were evaluated for ligation efficiency using TBE/agarose gel electrophoresis. The isolated MCNA-OTC product was equilibrated with Lipofectamine and transfected into adherent HEK293 cells. Unfractionated cell lysate was then assayed for citrulline production from ornithine and carbamoyl phosphate (FIG. 10).

MCNA-OTC

(SEQ ID NO: 24)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGCUGUUCA

ACCUUCGGAUCUUGCUGAACAACGCUGCGUUCCGGAAUGGUCACAACUUCA

UGGUCCGGAACUUCAGAUGCGGCCAGCCGCUCCAGAACAAGGUGCAGCUCA

AGGGGAGGGACCUCCUCACCCUGAAAAACUUCACCGGAGAAGAGAUCAAGU

ACAUGCUGUGGCUGUCAGCCGACCUCAAAUUCCGGAUCAAGCAGAAGGGCG

AAUACCUUCCUUUGCUGCAGGGAAAGUCCCUGGGGAUGAUCUUCGAGAAGC

GCAGCACUCGCACUAGACUGUCAACUGAAACCGGCUUCGCGCUGCUGGGAG

GACACCCCUGCUUCCUGACCACCCAAGAUAUCCAUCUGGGUGUGAACGAAU

CCCUCACCGACACAGCGCGGGUGCUGUCGUCCAUGGCAGACGCGGUCCUCG

CCCGCGUGUACAAGCAGUCUGAUCUGGACACUCUGGCCAAGGAAGCCUCCA

UUCCUAUCAUUAAUGGAUUGUCCGACCUCUACCAUCCCAUCCAGAUUCUGG

CCGAUUAUCUGACUCUGCAAGAACAUUACAGCUCCCUGAAGGGGCUUACCC

UUUCGUGGAUCGGCGACGGCAACAACAUUCUGCACAGCAUUAUGAUGAGCG

CUGCCAAGUUUGGAAUGCACCUCCAAGCAGCGACCCCGAAGGGAUACGAGC

CAGACGCCUCCGUGACGAAGCUGGCUGAGCAGUACGCCAAGGAGAACGGCA

CUAAGCUGCUGCUCACCAACGACCCUCUCGAAGCCGCCCACGGUGGCAACG

UGCUGAUCACCGAUACCUGGAUCUCCAUGGGACAGGAGGAGGAAAAGAAGA

AGCGCCUGCAAGCAUUUCAGGGGUACCAGGUGACUAUGAAAACCGCCAAGG

UCGCCGCCUCGGACUGGACCUUCUUGCACUGUCUGCCCAGAAAGCCCGAAG

AGGUGGACGACGAGGUGUUCUACAGCCCGCGGUCGCUGGUCUUUCCGGAGG

CCGAAAACAGGAAGUGGACUAUCAUGGCCGUGAUGGUGUCCCUGCUGACCG

AUUACUCCCCGCAGCUGCAGAAACCAAAGUUCUGACGGGUGGCAUCCCUGU

GACCCCUCCCCAGUGCCUCUCCUGGCCCUGGAAGUUGCCACUCCAGUGCCC

ACCAGCCUUGUCCUAAUAAAAUUAAGUUGCAUCAAGCU

UCGAACUACGUUGAAUUAAAAUAAU

CCUGUUCCGACCACCCGUGACCUCACCGUUGAAGGUCCCGGUCCUCUCCGU

GACCCCUCCCCAGUGUCCCUACGGUGGGCAGUCUUGAAACCAAAGACGUCG

ACGCCCCUCAUUAGCCAGUCGUCCCUGUGGUAGUGCCGGUACUAUCAGGUG

AAGGACAAAAGCCGGAGGCCUUUCUGGUCGCUGGCGCCCGACAUCUUGUGG

AGCAGCAGGUGGAGAAGCCCGAAAGACCCGUCUGUCACGUUCUUCCAGGUC

AGGCUCCGCCGCUGGAACCGCCAAAAGUAUCAGUGGACCAUGGGGACUUUA

CGAACGUCCGCGAAGAAGAAAAGGAGGAGGACAGGGUACCUCUAGGUCCAU

AGCCACUAGUCGUGCAACGGUGGCACCCGCCGAAGCUCUCCCAGCAACCAC

UCGUCGUCGAAUCACGGCAAGAGGAACCGCAUGACGAGUCGGUCGAAGCAG

UGCCUCCGCAGACCGAGCAUAGGGAAGCCCCAGCGACGAACCUCCACGUAA

GGUUUGAACCGUCGCGAGUAGUAUUACGACACGUCUUACAACAACGGCAGC

GGCUAGGUGCUUUCCCAUUCGGGGAAGUCCCUCGACAUUACAAGAACGUCU

CAGUCUAUUAGCCGGUCUUAGACCUACCCUACCAUCUCCAGCCUGUUAGGU

AAUUACUAUCCUUACCUCCGAAGGAACCGGUCUCACAGGUCUAGUCUGACG

AACAUGUGCGCCCGCUCCUGGCGCAGACGGUACCUGCUGUCGUGGGCGCGA

CACAGCCACUCCCUAAGCAAGUGUGGGUCUACCUAUAGAACCCACCAGUCC

UUCGUCCCCACAGGAGGGUCGUCGCGCUUCGGCCAAAGUCAACUGUCAGAU

CACGCUCACGACGCGAAGAGCUUCUAGUAGGGGUCCCUGAAAGGGACGUCG

UUUCCUUCCAUAAGCGGGAAGACGAACUAGGCCUUAAACUCCAGCCGACUG

UCGGUGUCGUACAUGAACUAGAGAAGAGGCCACUUCAAAAAGUCCCACUCC

UCCAGGGAGGGGAACUCGACGUGGAACAAGACCUCGCCGACCGGCGUAGAC

UUCAAGGCCUGGUACUUCAACACUGGUAAGGCCUUGCGUCGCAACAAGUCG

UUCUAGGCUUCCAACUUGUCGUAGCACAGUUCCUGCCACUCAGUGAGAACC

GUGCCCCUUAGGCGCAAGGUUACGUGGCAAGGGCCGGCGCCUCCGACCUAG

CCAGGGCCACAGAAGAUACCUCCAGUUUUGUCGCACCUACCGCAGAGGUCC

GCUAGACAGG-5' (Bold base are OMeRNA)

MCNA-PAH Preparation

MCNA-PAH comprising human Phenylalanine Hydroxylase (hPAH) RNA (SEQ ID NO: 25) was prepared by splint ligation of the 3′-end of two copies of an RNA encoding the hPAH protein to the 5′-ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hPAH was transcribed using RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hPAH transcript was then ligated in a single step to a 2′-hydroxymethylated RNA (OMeRNA) “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(oligo 1 (bridge) ; 5'- CGA CUC UCG G -3'-3'- G GCU

CUC AGC -5', bold bases OMeRNA)

using either T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and oligo 1 (oligo 2 (splint) (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). To prepare the samples for ligation, oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated oligo 1 (bridge) was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 2.7 μM capped hPAH transcript, 1.2 μM oligo 1 and 2.7 μM oligo 2 by heating to 75° C. for 5 minutes, followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 0.33 U/μL T4 RNA ligase 1. Each was reacted for 60 minutes at 37° C. The completed ligation reaction was then reacted with DNase I and subsequently purified using an RNeasy Maxi Kit (Qiagen). The reaction products were evaluated for ligation efficiency using TBE/agarose gel electrophoresis. The isolated MCNA-PAH reaction product was equilibrated with Lipofectamine and transfected into adherent HEK293 cells. Unfractionated cell lysate was then assayed for PAH protein expression using a PAH-specific ELISA (FIG. 11).

MCNA-PAH

(SEQ ID NO: 25)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGAGCACCG

CCGUGCUGGAGAACCCCGGCCUGGGCCGCAAGCUGAGCGACUUCGGCCAGG

AGACCAGCUACAUCGAGGACAACUGCAACCAGAACGGCGCCAUCAGCCUGA

UCUUCAGCCUGAAGGAGGAGGUGGGCGCCCUGGCCAAGGUGCUGCGCCUGU

UCGAGGAGAACGACGUGAACCUGACCCACAUCGAGAGCCGCCCCAGCCGCC

UGAAGAAGGACGAGUACGAGUUCUUCACCCACCUGGACAAGCGCAGCCUGC

CCGCCCUGACCAACAUCAUCAAGAUCCUGCGCCACGACAUCGGCGCCACCG

UGCACGAGCUGAGCCGCGACAAGAAGAAGGACACCGUGCCCUGGUUCCCCC

GCACCAUCCAGGAGCUGGACCGCUUCGCCAACCAGAUCCUGAGCUACGGCG

CCGAGCUGGACGCCGACCACCCCGGCUUCAAGGACCCCGUGUACCGCGCCC

GCCGCAAGCAGUUCGCCGACAUCGCCUACAACUACCGCCACGGCCAGCCCA

UCCCCCGCGUGGAGUACAUGGAGGAGGAGAAGAAGACCUGGGGCACCGUGU

UCAAGACCCUGAAGAGCCUGUACAAGACCCACGCCUGCUACGAGUACAACC

ACAUCUUCCCCCUGCUGGAGAAGUACUGCGGCUUCCACGAGGACAACAUCC

CCCAGCUGGAGGACGUGAGCCAGUUCCUGCAGACCUGCACCGGCUUCCGCC

UGCGCCCCGUGGCCGGCCUGCUGAGCAGCCGCGACUUCCUGGGCGGCCUGG

CCUUCCGCGUGUUCCACUGCACCCAGUACAUCCGCCACGGCAGCAAGCCCA

UGUACACCCCCGAGCCCGACAUCUGCCACGAGCUGCUGGGCCACGUGCCCC

UGUUCAGCGACCGCAGCUUCGCCCAGUUCAGCCAGGAGAUCGGCCUGGCCA

GCCUGGGCGCCCCCGACGAGUACAUCGAGAAGCUGGCCACCAUCUACUGGU

UCACCGUGGAGUUCGGCCUGUGCAAGCAGGGCGACAGCAUCAAGGCCUACG

GCGCCGGCCUGCUGAGCAGCUUCGGCGAGCUGCAGUACUGCCUGAGCGAGA

AGCCCAAGCUGCUGCCCCUGGAGCUGGAGAAGACCGCCAUCCAGAACUACA

CCGUGACCGAGUUCCAGCCCCUGUACUACGUGGCCGAGAGCUUCAACGACG

CCAAGGAGAAGGUGCGCAACUUCGCCGCCACCAUCCCCCGCCCCUUCAGCG

UGCGCUACGACCCCUACACCCAGCGCAUCGAGGUGCUGGACAACACCCAGC

AGCUGAAGAUCCUGGCCGACAGCAUCAACAGCGAGAUCGGCAUCCUGUGCA

GCGCCCUGCAGAAGAUCAAGUAACGGGUGGCAUCCCUGUGACCCCUCCCCA

GUGCCUCUCCUGGCCCUGGAAGUUGCCACUCCAGUGCCCACCAGCCUUGUC

CUAAUAAAAUUAAGUUGCAUCAAGCU

UCGAACUACGUUGAAUUAAAAUAAUCCUGUUCCGACCACC

CGUGACCUCACCGUUGAAGGUCCCGGUCCUCUCCGUGACCCCUCCCCAGUG

UCCCUACGGUGGGCAAUGAACUAGAAGACGUCCCGCGACGUGUCCUACGGC

UAGAGCGACAACUACGACAGCCGGUCCUAGAAGUCGACGACCCACAACAGG

UCGUGGAGCUACGCGACCCACAUCCCCAGCAUCGCGUGCGACUUCCCCGCC

CCCUACCACCGCCGCUUCAACGCGUGGAAGAGGAACCGCAGCAACUUCGAG

AGCCGGUGCAUCAUGUCCCCGACCUUGAGCCAGUGCCACAUCAAGACCUAC

CGCCAGAAGAGGUCGAGGUCCCCGUCGUCGAACCCGAAGAGCGAGUCCGUC

AUGACGUCGAGCGGCUUCGACGAGUCGUCCGGCCGCGGCAUCCGGAACUAC

GACAGCGGGACGAACGUGUCCGGCUUGAGGUGCCACUUGGUCAUCUACCAC

CGGUCGAAGAGCUACAUGAGCAGCCCCCGCGGGUCCGACCGGUCCGGCUAG

AGGACCGACUUGACCCGCUUCGACGCCAGCGACUUGUCCCCGUGCACCGGG

UCGUCGAGCACCGUCUACAGCCCGAGCCCCCACAUGUACCCGAACGACGGC

ACCGCCUACAUGACCCACGUCACCUUGUGCGCCUUCCGGUCCGGCGGGUCC

UUCAGCGCCGACGAGUCGUCCGGCCGGUGCCCCGCGUCCGCCUUCGGCCAC

GUCCAGACGUCCUUGACCGAGUGCAGGAGGUCGACCCCCUACAACAGGAGC

ACCUUCGGCGUCAUGAAGAGGUCGUCCCCCUUCUACACCAACAUGAGCAUC

GUCCGCACCCAGAACAUGUCCGAGAAGUCCCAGAACUUGUGCCACGGGGUC

CAGAAGAAGAGGAGGAGGUACAUGAGGUGCGCCCCCUACCCGACCGGCACC

GCCAUCAACAUCCGCUACAGCCGCUUGACGAACGCCGCCCGCGCCAUGUGC

CCCAGGAACUUCGGCCCCACCAGCCGCAGGUCGAGCCGCGGCAUCGAGUCC

UAGACCAACCGCUUCGCCAGGUCGAGGACCUACCACGCCCCCUUGGUCCCG

UGCCACAGGAAGAAGAACAGCGCCGAGUCGAGCACGUGCCACCGCGGCUAC

AGCACCGCGUCCUAGAACUACUACAACCAGUCCCGCCCGUCCGACGCGAAC

AGGUCCACCCACUUCUUGAGCAUGAGCAGGAAGAAGUCCGCCGACCCCGCC

GAGAGCUACACCCAGUCCAAGUGCAGCAAGAGGAGCUUGUCCGCGUCGUGG

AACCGGUCCCGCGGGUGGAGGAGGAAGUCCGACUUCUAGUCCGACUACCGC

GGCAAGACCAACGUCAACAGGAGCUACAUCGACCAGAGGACCGGCUUCAGC

GAGUCGAACGCCGGGUCCGGCCCCAAGAGGUCGUGCCGCCACGAGUAGCAC

AGUUCCUGCCACUCAGUGAGAACCGUGCCCCUUAGGCGCAAGGUUACGUGG

CAAGGGCCGGCGCCUCCGACCUAGCCAGGGCCACAGAAGAUACCUCCAGUU

UUGUCGCACCUACCGCAGAGGUCCGCUAGACAGG-5'

(Bold base are OMeRNA)

MCNA-CFTR Preparation

MCNA-CFTR comprising human Cystic Fibrosis Transmembrane Conductance Regulator (hCFTR) RNA (SEQ ID NO: 26) was prepared by splint ligation of the 3′-end of two copies of an RNA encoding the hCFTR protein to the 5′-ends of a single oligonucleotide containing two 5′ ends and a linked 3′-3′ phosphodiester bond within the sequence. Briefly, a 5′-capped RNA containing a 5′-untranslated region (UTR) and a 3′ UTR flanking an RNA sequence encoding hCFTR was transcribed using RNA polymerase, enzymatically capped to contain a 5′-Cap 1 structure and purified. This hCFTR transcript was then ligated in a single step to a 2′-hydroxymethylated RNA (OMeRNA) “bridge” oligonucleotide containing a 20 nucleotide (nt) palindromic sequence with a 3′-3′ phosphodiester linkage between the 10^thand 11^thnt
(SEQ ID NO: 5)

(oligo 1 (bridge); 5'- CGA CUC UCG G -3'-3'- G GCU

CUC AGC -5', bold bases OMeRNA)

using either T4 RNA ligase 1+PEG 8K and a DNA oligonucleotide “splint” complementary to the 3′-UTR and oligo 1 (oligo 2 (splint) (SEQ ID NO: 9); 5′ CCG AGA GTC GAG CTT GAT GCA ACT TAA TTT TAT TAG G 3′; all bases DNA). To prepare the samples for ligation, oligo 1 was 5′-end phosphorylated in a reaction containing 50 μM oligo 1, 1 mM ATP, 1×PNK Buffer (NEB; 70 mM Tris-HCl, 10 mM MgCl₂, 5 mM DTT pH 7.6 at 25° C.) and 0.5 U/μL T4 Polynucleotide Kinase (NEB) at 37° C. for 1 hour. Phosphorylated oligo 1 (bridge) was then desalted using a Sephadex G-25 desalting column (Princeton Separations) and hybridized to the transcript and splint in a reaction containing 0.92 μM capped hCFTR transcript, 0.42 μM oligo 1 and 0.92 μM oligo 2 by heating to 75° C. for 5 minutes followed by gradual cooling to room temperature over 5 minutes. An RNA ligation reaction was subsequently prepared to contain a 50% diluted hybridization reaction and 1×RNA ligase Buffer (NEB; 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT pH 7.5 at 25° C.), 1 mM ATP, 10% PEG and 0.33 U/μL T4 RNA ligase 1. Each was reacted for 60 minutes at 37° C. The completed ligation reaction was then reacted with DNase I and subsequently purified using an RNeasy Maxi Kit (Qiagen). The reaction products were evaluated for ligation efficiency using TBE/agarose gel electrophoresis. The isolated MCNA-CFTR product was equilibrated with Lipofectamine and transfected into adherent HEK293 cells. Unfractionated cell lysate was then assayed for CFTR protein expression using CFTR-specific Western Blotting (FIG. 12).

MCNA-CFTR

(SEQ ID NO: 26)

5'-GGACAGAUCGCCUGGAGACGCCAUCCACGCUGUUUUGACCUCCAUAGA

AGACACCGGGACCGAUCCAGCCUCCGCGGCCGGGAACGGUGCAUUGGAACG

CGGAUUCCCCGUGCCAAGAGUGACUCACCGUCCUUGACACGAUGCAACGCU

CUCCUCUUGAAAAGGCCUCGGUGGUGUCCAAGCUCUUCUUCUCGUGGACUA

GACCCAUCCUGAGAAAGGGGUACAGACAGCGCUUGGAGCUGUCCGAUAUCU

AUCAAAUCCCUUCCGUGGACUCCGCGGACAACCUGUCCGAGAAGCUCGAGA

GAGAAUGGGACAGAGAACUCGCCUCAAAGAAGAACCCGAAGCUGAUUAAUG

CGCUUAGGCGGUGCUUUUUCUGGCGGUUCAUGUUCUACGGCAUCUUCCUCU

ACCUGGGAGAGGUCACCAAGGCCGUGCAGCCCCUGUUGCUGGGACGGAUUA

UUGCCUCCUACGACCCCGACAACAAGGAAGAAAGAAGCAUCGCUAUCUACU

UGGGCAUCGGUCUGUGCCUGCUUUUCAUCGUCCGGACCCUCUUGUUGCAUC

CUGCUAUUUUCGGCCUGCAUCACAUUGGCAUGCAGAUGAGAAUUGCCAUGU

UUUCCCUGAUCUACAAGAAAACUCUGAAGCUCUCGAGCCGCGUGCUUGACA

AGAUUUCCAUCGGCCAGCUCGUGUCCCUGCUCUCCAACAAUCUGAACAAGU

UCGACGAGGGCCUCGCCCUGGCCCACUUCGUGUGGAUCGCCCCUCUGCAAG

UGGCGCUUCUGAUGGGCCUGAUCUGGGAGCUGCUGCAAGCCUCGGCAUUCU

GUGGGCUUGGAUUCCUGAUCGUGCUGGCACUGUUCCAGGCCGGACUGGGGC

GGAUGAUGAUGAAGUACAGGGACCAGAGAGCCGGAAAGAUUUCCGAACGGC

UGGUGAUCACUUCGGAAAUGAUCGAAAACAUCCAGUCAGUGAAGGCCUACU

GCUGGGAAGAGGCCAUGGAAAAGAUGAUUGAAAACCUCCGGCAAACCGAGC

UGAAGCUGACCCGCAAGGCCGCUUACGUGCGCUAUUUCAACUCGUCCGCUU

UCUUCUUCUCCGGGUUCUUCGUGGUGUUUCUCUCCGUGCUCCCCUACGCCC

UGAUUAAGGGAAUCAUCCUCAGGAAGAUCUUCACCACCAUUUCCUUCUGUA

UCGUGCUCCGCAUGGCCGUGACCCGGCAGUUCCCAUGGGCCGUGCAGACUU

GGUACGACUCCCUGGGAGCCAUUAACAAGAUCCAGGACUUCCUUCAAAAGC

AGGAGUACAAGACCCUCGAGUACAACCUGACUACUACCGAGGUCGUGAUGG

AAAACGUCACCGCCUUUUGGGAGGAGGGAUUUGGCGAACUGUUCGAGAAGG

CCAAGCAGAACAACAACAACCGCAAGACCUCGAACGGUGACGACUCCCUCU

UCUUUUCAAACUUCAGCCUGCUCGGGACGCCCGUGCUGAAGGACAUUAACU

UCAAGAUCGAAAGAGGACAGCUCCUGGCGGUGGCCGGAUCGACCGGAGCCG

GAAAGACUUCCCUGCUGAUGGUGAUCAUGGGAGAGCUUGAACCUAGCGAGG

GAAAGAUCAAGCACUCCGGCCGCAUCAGCUUCUGUAGCCAGUUUUCCUGGA

UCAUGCCCGGAACCAUUAAGGAAAACAUCAUCUUCGGCGUGUCCUACGAUG

AAUACCGCUACCGGUCCGUGAUCAAAGCCUGCCAGCUGGAAGAGGAUAUUU

CAAAGUUCGCGGAGAAAGAUAACAUCGUGCUGGGCGAAGGGGGUAUUACCU

UGUCGGGGGGCCAGCGGGCUAGAAUCUCGCUGGCCAGAGCCGUGUAUAAGG

ACGCCGACCUGUAUCUCCUGGACUCCCCCUUCGGAUACCUGGACGUCCUGA

CCGAAAAGGAGAUCUUCGAAUCGUGCGUGUGCAAGCUGAUGGCUAACAAGA

CUCGCAUCCUCGUGACCUCCAAAAUGGAGCACCUGAAGAAGGCAGACAAGA

UUCUGAUUCUGCAUGAGGGGUCCUCCUACUUUUACGGCACCUUCUCGGAGU

UGCAGAACUUGCAGCCCGACUUCUCAUCGAAGCUGAUGGGUUGCGACAGCU

UCGACCAGUUCUCCGCCGAAAGAAGGAACUCGAUCCUGACGGAAACCUUGC

ACCGCUUCUCUUUGGAAGGCGACGCCCCUGUGUCAUGGACCGAGACUAAGA

AGCAGAGCUUCAAGCAGACCGGGGAAUUCGGCGAAAAGAGGAAGAACAGCA

UCUUGAACCCCAUUAACUCCAUCCGCAAGUUCUCAAUCGUGCAAAAGACGC

CACUGCAGAUGAACGGCAUUGAGGAGGACUCCGACGAACCCCUUGAGAGGC

GCCUGUCCCUGGUGCCGGACAGCGAGCAGGGAGAAGCCAUCCUGCCUCGGA

UUUCCGUGAUCUCCACUGGUCCGACGCUCCAAGCCCGGCGGCGGCAGUCCG

UGCUGAACCUGAUGACCCACAGCGUGAACCAGGGCCAAAACAUUCACCGCA

AGACUACCGCAUCCACCCGGAAAGUGUCCCUGGCACCUCAAGCGAAUCUUA

CCGAGCUCGACAUCUACUCCCGGAGACUGUCGCAGGAAACCGGGCUCGAAA

UUUCCGAAGAAAUCAACGAGGAGGAUCUGAAAGAGUGCUUCUUCGACGAUA

UGGAGUCGAUACCCGCCGUGACGACUUGGAACACUUAUCUGCGGUACAUCA

CUGUGCACAAGUCAUUGAUCUUCGUGCUGAUUUGGUGCCUGGUGAUUUUCC

UGGCCGAGGUCGCGGCCUCACUGGUGGUGCUCUGGCUGUUGGGAAACACGC

CUCUGCAAGACAAGGGAAACUCCACGCACUCGAGAAACAACAGCUAUGCCG

UGAUUAUCACUUCCACCUCCUCUUAUUACGUGUUCUACAUCUACGUCGGAG

UGGCGGAUACCCUGCUCGCGAUGGGUUUCUUCAGAGGACUGCCGCUGGUCC

ACACCUUGAUCACCGUCAGCAAGAUUCUUCACCACAAGAUGUUGCAUAGCG

UGCUGCAGGCCCCCAUGUCCACCCUCAACACUCUGAAGGCCGGAGGCAUUC

UGAACAGAUUCUCCAAGGACAUCGCUAUCCUGGACGAUCUCCUGCCGCUUA

CCAUCUUUGACUUCAUCCAGCUGCUGCUGAUCGUGAUUGGAGCAAUCGCAG

UGGUGGCGGUGCUGCAGCCUUACAUUUUCGUGGCCACUGUGCCGGUCAUUG

UGGCGUUCAUCAUGCUGCGGGCCUACUUCCUCCAAACCAGCCAGCAGCUGA

AGCAACUGGAAUCCGAGGGACGAUCCCCCAUCUUCACUCACCUUGUGACGU

CGUUGAAGGGACUGUGGACCCUCCGGGCUUUCGGACGGCAGCCCUACUUCG

AAACCCUCUUCCACAAGGCCCUGAACCUCCACACCGCCAAUUGGUUCCUGU

ACCUGUCCACCCUGCGGUGGUUCCAGAUGCGCAUCGAGAUGAUUUUCGUCA

UCUUCUUCAUCGCGGUCACAUUCAUCAGCAUCCUGACUACCGGAGAGGGAG

AGGGACGGGUCGGAAUAAUCCUGACCCUCGCCAUGAACAUUAUGAGCACCC

UGCAGUGGGCAGUGAACAGCUCGAUCGACGUGGACAGCCUGAUGCGAAGCG

UCAGCCGCGUGUUCAAGUUCAUCGACAUGCCUACUGAGGGAAAACCCACUA

AGUCCACUAAGCCCUACAAAAAUGGCCAGCUGAGCAAGGUCAUGAUCAUCG

AAAACUCCCACGUGAAGAAGGACGAUAUUUGGCCCUCCGGAGGUCAAAUGA

CCGUGAAGGACCUGACCGCAAAGUACACCGAGGGAGGAAACGCCAUUCUCG

AAAACAUCAGCUUCUCCAUUUCGCCGGGACAGCGGGUCGGCCUUCUCGGGC

GGACCGGUUCCGGGAAGUCAACUCUGCUGUCGGCUUUCCUCCGGCUGCUGA

AUACCGAGGGGGAAAUCCAAAUUGACGGCGUGUCUUGGGAUUCCAUUACUC

UGCAGCAGUGGCGGAAGGCCUUCGGCGUGAUCCCCCAGAAGGUGUUCAUCU

UCUCGGGUACCUUCCGGAAGAACCUGGAUCCUUACGAGCAGUGGAGCGACC

AAGAAAUCUGGAAGGUCGCCGACGAGGUCGGCCUGCGCUCCGUGAUUGAAC

AAUUUCCUGGAAAGCUGGACUUCGUGCUCGUCGACGGGGGAUGUGUCCUGU

CGCACGGACAUAAGCAGCUCAUGUGCCUCGCACGGUCCGUGCUCUCCAAGG

CCAAGAUUCUGCUGCUGGACGAACCUUCGGCCCACCUGGAUCCGGUCACCU

ACCAGAUCAUCAGGAGGACCCUGAAGCAGGCCUUUGCCGAUUGCACCGUGA

UUCUCUGCGAGCACCGCAUCGAGGCCAUGCUGGAGUGCCAGCAGUUCCUGG

UCAUCGAGGAGAACAAGGUCCGCCAAUACGACUCCAUUCAAAAGCUCCUCA

ACGAGCGGUCGCUGUUCAGACAAGCUAUUUCACCGUCCGAUAGAGUGAAGC

UCUUCCCGCAUCGGAACAGCUCAAAGUGCAAAUCGAAGCCGCAGAUCGCAG

CCUUGAAGGAAGAGACUGAGGAAGAGGUGCAGGACACCCGGCUUUAACGGG

UGGCAUCCCUGUGACCCCUCCCCAGUGCCUCUCCUGGCCCUGGAAGUUGCC

ACUCCAGUGCCCACCAGCCUUGUCCUAAUAAAAUUAAGUUGCAUCAAGCU

UCGAACUACGUUGAAUUA

AAAUAAUCCUGUUCCGACCACCCGUGACCUCACCGUUGAAGGUCCCGGUCC

UCUCCGUGACCCCUCCCCAGUGUCCCUACGGUGGGCAAUUUCGGCCCACAG

GACGUGGAGAAGGAGUCAGAGAAGGAAGUUCCGACGCUAGACGCCGAAGCU

AAACGUGAAACUCGACAAGGCUACGCCCUUCUCGAAGUGAGAUAGCCUGCC

ACUUUAUCGAACAGACUUGUCGCUGGCGAGCAACUCCUCGAAAACUUACCU

CAGCAUAACCGCCUGGAACAAGAGGAGCUACUGGUCCUUGACGACCGUGAG

GUCGUACCGGAGCUACGCCACGAGCGUCUCUUAGUGCCACGUUAGCCGUUU

CCGGACGAAGUCCCAGGAGGACUACUAGACCAUCCACUGGCCUAGGUCCAC

CCGGCUUCCAAGCAGGUCGUCGUCUUAGAACCGGAACCUCUCGUGCCUGGC

ACGCUCCGUGUACUCGACGAAUACAGGCACGCUGUCCUGUGUAGGGGGCAG

CUGCUCGUGCUUCAGGUCGAAAGGUCCUUUAACAAGUUAGUGCCUCGCGUC

CGGCUGGAGCAGCCGCUGGAAGGUCUAAAGAACCAGCGAGGUGACGAGCAU

UCCUAGGUCCAAGAAGGCCUUCCAUGGGCUCUUCUACUUGUGGAAGACCCC

CUAGUGCGGCUUCCGGAAGGCGGUGACGACGUCUCAUUACCUUAGGGUUCU

GUGCGGCAGUUAAACCUAAAGGGGGAGCCAUAAGUCGUCGGCCUCCUUUCG

GCUGUCGUCUCAACUGAAGGGCCUUGGCCAGGCGGGCUCUUCCGGCUGGGC

GACAGGGCCGCUUUACCUCUUCGACUACAAAAGCUCUUACCGCAAAGGAGG

GAGCCACAUGAAACGCCAGUCCAGGAAGUGCCAGUAAACUGGAGGCCUCCC

GGUUUAUAGCAGGAAGAAGUGCACCCUCAAAAGCUACUAGUACUGGAACGA

GUCGACCGGUAAAAACAUCCCGAAUCACCUGAAUCACCCAAAAGGGAGUCA

UCCGUACAGCUACUUGAACUUGUGCGCCGACUGCGAAGCGUAGUCCGACAG

GUGCAGCUAGCUCGACAAGUGACGGGUGACGUCCCACGAGUAUUACAAGUA

CCGCUCCCAGUCCUAAUAAGGCUGGGCAGGGAGAGGGAGAGGCCAUCAGUC

CUACGACUACUUACACUGGCGCUACUUCUUCUACUGCUUUUAGUAGAGCUA

CGCGUAGACCUUGGUGGCGUCCCACCUGUCCAUGUCCUUGGUUAACCGCCA

CACCUCCAAGUCCCGGAACACCUUCUCCCAAAGCUUCAUCCCGACGGCAGG

CUUUCGGGCCUCCCAGGUGUCAGGGAAGUUGCUGCAGUGUUCCACUCACUU

CUACCCCCUAGCAGGGAGCCUAAGGUCAACGAAGUCGACGACCGACCAAAC

CUCCUUCAUCCGGGCGUCGUACUACUUGCGGUGUUACUGGCCGUGUCACCG

GUGCUUUUACAUUCCGACGUCGUGGCGGUGGUGACGCUAACGAGGUUAGUG

CUAGUCGUCGUCGACCUACUUCAGUUUCUACCAUUCGCCGUCCUCUAGCAG

GUCCUAUCGCUACAGGAACCUCUUAGACAAGUCUUACGGAGGCCGGAAGUC

UCACAACUCCCACCUGUACCCCCGGACGUCGUGCGAUACGUUGUAGAACAC

CACUUCUUAGAACGACUGCCACUAGUUCCACACCUGGUCGCCGUCAGGAGA

CUUCUUUGGGUAGCGCUCGUCCCAUAGGCGGUGAGGCUGCAUCUACAUCUU

GUGCAUUAUUCUCCUCCACCUUCACUAUUAGUGCCGUAUCGACAACAAAGA

GCUCACGCACCUCAAAGGGAACAGAACGUCUCCGCACAAAGGGUUGUCGGU

CUCGUGGUGGUCACUCCGGCGCUGGAGCCGGUCCUUUUAGUGGUCCGUGGU

UUAGUCGUGCUUCUAGUUACUGAACACGUGUCACUACAUGGCGUCUAUUCA

CAAGGUUCAGCAGUGCCGCCCAUAGCUGAGGUAUAGCAGCUUCUUCGUGAG

AAAGUCUAGGAGGAGCAACUAAAGAAGCCUUUAAAGCUCGGGCCAAAGGAC

GCUGUCAGAGGCCCUCAUCUACAGCUCGAGCCAUUCUAAGCGAACUCCACG

GUCCCUGUGAAAGGCCCACCUACGCCAUCAGAACGCCACUUACAAAACCGG

GACCAAGUGCGACACCCAGUAGUCCAAGUCGUGCCUGACGGCGGCGGCCCG

AACCUCGCAGCCUGGUCACCUCUAGUGCCUUUAGGCUCCGUCCUACCGAAG

AGGGACGAGCGACAGGCCGUGGUCCCUGUCCGCGGAGAGUUCCCCAAGCAG

CCUCAGGAGGAGUUACGGCAAGUAGACGUCACCGCAGAAAACGUGCUAACU

CUUGAACGCCUACCUCAAUUACCCCAAGUUCUACGACAAGAAGGAGAAAAG

CGGCUUAAGGGGCCAGACGAACUUCGAGACGAAGAAUCAGAGCCAGGUACU

GUGUCCCCGCAGCGGAAGGUUUCUCUUCGCCACGUUCCAAAGGCAGUCCUA

GCUCAAGGAAGAAAGCCGCCUCUUGACCAGCUUCGACAGCGUUGGGUAGUC

GAAGCUACUCUUCAGCCCGACGUUCAAGACGUUGAGGCUCUUCCACGGCAU

UUUCAUCCUCCUGGGGAGUACGUCUUAGUCUUAGAACAGACGGAAGAAGUC

CACGAGGUAAAACCUCCAGUGCUCCUACGCUCAGAACAAUCGGUAGUCGAA

CGUGUGCGUGCUAAGCUUCUAGAGGAAAAGCCAGUCCUGCAGGUCCAUAGG

CUUCCCCCUCAGGUCCUCUAUGUCCAGCCGCAGGAAUAUGUGCCGAGACCG

GUCGCUCUAAGAUCGGGCGACCGGGGGGCUGUUCCAUUAUGGGGGAAGCGG

GUCGUGCUACAAUAGAAAGAGGCGCUUGAAACUUUAUAGGAGAAGGUCGAC

CGUCCGAAACUAGUGCCUGGCCAUCGCCAUAAGUAGCAUCCUGUGCGGCUU

CUACUACAAAAGGAAUUACCAAGGCCCGUACUAGGUCCUUUUGACCGAUGU

CUUCGACUACGCCGGCCUCACGAACUAGAAAGGGAGCGAUCCAAGUUCGAG

AGGGUACUAGUGGUAGUCGUCCCUUCAGAAAGGCCGAGGCCAGCUAGGCCG

GUGGCGGUCCUCGACAGGAGAAAGCUAGAACUUCAAUUACAGGAAGUCGUG

CCCGCAGGGCUCGUCCGACUUCAAACUUUUCUUCUCCCUCAGCAGUGGCAA

GCUCCAGAACGCCAACAACAACAAGACGAACCGGAAGAGCUUGUCAAGCGG

UUUAGGGAGGAGGGUUUUCCGCCACUGCAAAAGGUAGUGCUGGAGCCAUCA

UCAGUCCAACAUGAGCUCCCAGAACAUGAGGACGAAAACUUCCUUCAGGAC

CUAGAACAAUUACCGAGGGUCCCUCAGCAUGGUUCAGACGUGCCGGGUACC

CUUGACGGCCCAGUGCCGGUACGCCUCGUGCUAUGUCUUCCUUUACCACCA

CUUCUAGAAGGACUCCUACUAAGGGAAUUAGUCCCGCAUCCCCUCGUGCCU

CUCUUUGUGGUGCUUCUUGGGCCUCUUCUUCUUUCGCCUGCUCAACUUUAU

CGCGUGCAUUCGCCGGAACGCCCAGUCGAAGUCGAGCCAAACGGCCUCCAA

AAGUUAGUAGAAAAGGUACCGGAGAAGGGUCGUCAUCCGGAAGUGACUGAC

CUACAAAAGCUAGUAAAGGCUUCACUAGUGGUCGGCAAGCCUUUAGAAAGG

CCGAGAGACCAGGGACAUGAAGUAGUAGUAGGCGGGGUCAGGCCGGACCUU

GUCACGGUCGUGCUAGUCCUUAGGUUCGGGUGUCUUACGGCUCCGAACGUC

GUCGAGGGUCUAGUCCGGGUAGUCUUCGCGGUGAACGUCUCCCCGCUAGGU

GUGCUUCACCCGGUCCCGCUCCGGGAGCAGCUUGAACAAGUCUAACAACCU

CUCGUCCCUGUGCUCGACCGGCUACCUUUAGAACAGUUCGUGCGCCGAGCU

CUCGAAGUCUCAAAAGAACAUCUAGUCCCUUUUGUACCGUUAAGAGUAGAC

GUACGGUUACACUACGUCCGGCUUUUAUCGUCCUACGUUGUUCUCCCAGGC

CUGCUACUUUUCGUCCGUGUCUGGCUACGGGUUCAUCUAUCGCUACGAAGA

AAGAAGGAACAACAGCCCCAGCAUCCUCCGUUAUUAGGCAGGGUCGUUGUC

CCCGACGUGCCGGAACCACUGGAGAGGGUCCAUCUCCUUCUACGGCAUCUU

GUACUUGGCGGUCUUUUUCGUGGCGGAUUCGCGUAAUUAGUCGAAGCCCAA

GAAGAAACUCCGCUCAAGAGACAGGGUAAGAGAGAGCUCGAAGAGCCUGUC

CAACAGGCGCCUCAGGUGCCUUCCCUAAACUAUCUAUAGCCUGUCGAGGUU

CGCGACAGACAUGGGGAAAGAGUCCUACCCAGAUCAGGUGCUCUUCUUCUC

GAACCUGUGGUGGCUCCGGAAAAGUUCUCCUCUCGCAACGUAGCACAGUUC

CUGCCACUCAGUGAGAACCGUGCCCCUUAGGCGCAAGGUUACGUGGCAAGG

GCCGGCGCCUCCGACCUAGCCAGGGCCACAGAAGAUACCUCCAGUUUUGUC

GCACCUACCGCAGAGGUCCGCUAGACAGG-5'

(Bold base are OMeRNA)

Example 2. Exemplary Protein Production with MCNA

This example demonstrates the production of protein encoded by mRNA linked by their 3′ ends to a bridging oligonucleotide.
MCNA comprising human erythropoietin (hEPO) mRNA were synthesized as described above and used to transfect HEK293T cells (1 microgram RNA transfection per sample). FIG. 7 shows the results of an experiment comparing the amount of secreted hEPO protein from HEK293T cells when the cells were transfected with either a) mRNA encoding hEPO that lacked a polyA tail, b) MCNA comprising hEPO mRNA, or c) MCNA comprising hEPO mRNA that had been treated with DNase. A clear increase in protein production was achieved when the cells were transfected with either the MCNA comprising hEPO mRNA or the DNase-treated MCNA comprising hEPO mRNA compared to the untailed hEPO mRNA.
FIG. 9 shows the results of an experiment comparing the amount of secreted hEPO protein from HEK293T cells when the cells were transfected with either a) mRNA encoding hEPO that lacked a polyA tail, b) unpurified mixture of MCNA comprising hEPO mRNA with unreacted/partially reacted EPO RNA, c) purified unreacted/partially reacted EPO RNA, or d) purified EPO MCNA. All samples were transfected with a total of 250 nanograms RNA. A clear increase in protein production was achieved when the cells were transfected with purified EPO MCNA compared to the mixture or unreacted hEPO RNA. FIG. 10 shows the results of an experiment comparing the amount of human OTC protein activity (as measured by citrulline production) within HEK293T cells when the cells were transfected with either a) mRNA encoding hOTC that lacked a polyA tail (hOTC monomer), or b) MCNA comprising hOTC mRNA. Detectable protein production was achieved only when the cells were transfected with the MCNA comprising hOTC as compared to the hOTC monomer.
FIG. 11 shows the results of an experiment comparing the amount of human PAH protein produced within HEK293T cells when the cells were transfected with either a) mRNA encoding hPAH that lacked a polyA tail (hPAH monomer), or b) MCNA comprising hPAH mRNA. Significantly higher protein production was achieved when the cells were transfected with the MCNA comprising hPAH as compared to the hPAH monomer.
FIG. 12 shows the results of an experiment comparing the amount of human CFTR protein produced within HEK293T cells when the cells were transfected with either a) mRNA encoding hCFTR that lacked a polyA tail (hCFTR monomer), or b) MCNA comprising hCFTR mRNA. Detectable protein production was achieved only when the cells were transfected with the MCNA comprising hCFTR as compared to the hCFTR monomer.

Example 3. Exemplary In Vivo Protein Production with MCNA

This example demonstrates the in vivo production of protein encoded by mRNA linked by their 3′ ends to a bridging oligonucleotide.
MCNA comprising human ornithine carbamoyltransferase (hOTC) mRNA were synthesized as described above. spf^ashmice were treated intravenously with hOTC MCNA encapsulated in lipid nanoparticles. Animals were sacrificed and their livers were isolated either 24 hours or 7 days post-administration. Citrulline production was measured in the liver samples and it was found that the level of hOTC protein activity 7 days post-administration was comparable to the level of hOTC protein activity 24 hours post-administration (FIG. 13). At both time points, hOTC protein activity was significantly greater than in the livers of control spf^ashmice. Further, substantial hOTC protein was detected via Western blot at both 1 day and 8 days post-administration, but for only the spf^ashmice treated with hOTC MCNA LNPs, not the mice treated with the hOTC monomer LNPs (FIG. 14), consistent with the observed activity data. In comparison, when spf^ashmice were treated intravenously with hOTC mRNA, levels of hOTC protein activity were higher 24 hours post-administration than they were 7 days post-administration (FIG. 15). As clearly shown in FIG. 16, when hOTC protein activity 7 day post-administration was calculated as a percentage of activity levels after 24 hours, more sustained in vivo activity is observed for hOTC MCNA (109% of 24 hour activity) than for hOTC mRNA (38% of 24 hour activity).
In another study, MCNA comprising human phenylalanine hydroxylase (hPAH) were synthesized as described above. PAH knock-out (KO) mice were treated intravenously with either hPAH MCNA or an hPAH monomer (hPAH mRNA with a 5′ cap but without a polyA tail) encapsulated in lipid nanoparticles. Animals were sacrificed and their livers were isolated 24 hours post-administration. More than 27 times more hPAH protein was detected in the livers of mice treated with hPAH MCNA than was detected in the livers of mice treated with the hPAH monomer (FIG. 17).
Further, a demonstration of efficacy was achieved after treatment of PAH knock-out (KO) mice with hPAH MCNA LNPs. Specifically, serum phenylalanine levels were significantly reduced 24 hours after treatment with hPAH MCNA while no reduction in serum phenylalanine was seen 24 hours after treatment with hPAH monomer LNPs (FIG. 18).
In another study, MCNA comprising human erythropoietin (hEPO) were synthesized as described above. Wild-type mice were treated intravenously with either hEPO MCNA or an hEPO monomer (hEPO mRNA with a 5′ cap but without a polyA tail) encapsulated in lipid nanoparticles. Serum samples from the animals were obtained 24 hours post-administration. More than 480 times more hEPO protein was detected in the serum of mice treated with hEPO MCNA than was detected in the serum of mice treated with the hEPO monomer (FIG. 19).
In another study, MCNA comprising human cystic fibrosis transmembrane conductance regulator (hCFTR) were synthesized as described above. CFTR KO mice were treated via aerosolization of hCFTR MCNA encapsulated in lipid nanoparticles. Animals were sacrificed and their lungs were isolated either 24 hours or 7 days post-administration. As shown in FIG. 20, MCNA-derived hCFTR protein was detected in both the bronchial epithelial airways (top row) as well as alveolar regions (bottom row) both 24 hours and 7 days post-administration (brown staining).

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. The scope of the present invention is not intended to be limited to the above Description, but rather is as set forth in the following claims:

Claims

1. A multimeric coding nucleic acid (MCNA) comprising two polynucleotides linked via 3′ ends via an oligonucleotide bridge comprising a stable 3-3′ inverted phosphodiester linkage such that the multimeric coding nucleic acid compound comprises two or more 5′ ends, and

wherein at least one of the two polynucleotides is an encoding polynucleotide.

2.-4. (canceled)

5. The MCNA of claim 1, wherein the at least one encoding polynucleotide encodes a protein of interest.

6. The MCNA of claim 5, wherein the two polynucleotides are encoding polynucleotides, and each of the two encoding polynucleotides encodes the same protein.

7. The MCNA of claim 5, wherein the two polynucleotides are encoding polynucleotides, and each of the two encoding polynucleotides encodes a distinct protein.

8.-11. (canceled)

12. The MCNA of claim 1, wherein the at least one encoding polynucleotide comprises a 3′ UTR.

13. (canceled)

14. The MCNA of claim 12, wherein the 3′ UTR comprises a plurality of multi-A segments with spacers in between.

15.-26. (canceled)

27. The MCNA of claim 1, wherein the nucleosides comprising the oligonucleotide bridge are selected from the group consisting of 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ψU), and 1-methyl-pseudouridine.

28.-30. (canceled)

31. The MCNA of claim 1, wherein the at least one encoding polynucleotide comprises one or more modified nucleosides.

32. The MCNA of claim 31, wherein the modified nucleosides are selected from the group consisting of 2′-OMe-A, 2′-OMe-G, 2′-OMe-C, 2′-OMe-U, 2′-F-A, 2′-F-G, 2′-F-C, 2′-F-U, LNA-A, LNA-G, LNA-C, LNA-U, N6-methyl-adenosine, 2-thiouridine (2sU), 5-methyl-cytidine (5mC), pseudouridine (ψU), and 1-methyl-pseudouridine.

33.-38. (canceled)

39. The MCNA of claim 1, wherein the at least one or more encoding polynucleotides comprise a polynucleotide that encodes an enzyme, a receptor, a ligand, a light chain or heavy chain of an antibody, a nuclease, or a DNA-binding protein.

40. (canceled)

41. A composition comprising the MCNA of claim 1 encapsulated or complexed with a delivery vehicle.

42. The composition of claim 41, wherein the delivery vehicle is selected from the group consisting of liposomes, lipid nanoparticles, solid-lipid nanoparticles, polymers, viruses, sol-gels, and nanogels.

43.-47. (canceled)

48. The MCNA of claim 12, wherein the 3′ UTR does not include a polyA tail.

49. The MCNA of claim 1, at least one of the two polynucleotides is unmodified.

50. The MCNA of claim 1, wherein the oligonucleotide bridge is unmodified.

51. The MCNA of claim 1, wherein at least one of the two polynucleotides has a 5′ cap.

52. The MCNA of claim 1, wherein the second polynucleotide is an non-coding polynucleotide.

53. The MCNA of claim 1, wherein the MCNA comprises a second encoding polynucleotide.