WO2002018418A1 - Antibodies specific for methylated lysines in histones - Google Patents
Antibodies specific for methylated lysines in histones Download PDFInfo
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- WO2002018418A1 WO2002018418A1 PCT/US2001/026283 US0126283W WO0218418A1 WO 2002018418 A1 WO2002018418 A1 WO 2002018418A1 US 0126283 W US0126283 W US 0126283W WO 0218418 A1 WO0218418 A1 WO 0218418A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6875—Nucleoproteins
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
Definitions
- the present invention is directed to antibodies that bind to histone epitopes created by posfranslational modification of the histone protein, compositions comprising such antibodies, and the use of such compositions as diagnostic and screening tools.
- DNA is complexed with histone proteins to form nucleosomes, the repeating subunits of chromatin.
- This packaging of DNA imposes a severe restriction to proteins seeking access to DNA for DNA-templated processes such as transcription or replication. It is becoming increasingly clear that post- translational modifications of histone amino-termini play an important role in determining the chromatin structure of the eukaryotic Cell genome as well as regulating the expression of cellular genes.
- Chromosomes in higher eukaryotes have historically been considered to consist of regions of euchromatin and heterochromatin, which are distinguished by the degree of condensation and level of transcriptional activity of the underlying DNA sequences. Certain regions of constitutive heterochromatin are found at or near specialized structures such as centromeres, and are comprised mostly of genetically inert repetitive sequences. In contrast, other regions that have the same primary DNA sequences can exhibit characteristics of either type of chromatin, suggesting that epigenetic factors, such as packaging of DNA by histones and chromatin associated proteins, dictate the heterochromatin status at these loci.
- histone proteins contribute to a mechanism that can alter chromatin structure, thereby leading to inherited differences in transcriptional "on-off” states or to the stable propagation of chromosomes by defining a specialized higher-order structure.
- Histone methylation is one of the least-understood posttranslational modifications affecting histones.
- H3 and H4 are the primary histones modified by methylation
- sequencing studies, using bulk histones have shown that several lysines (e.g., 9 and 27 of H3 and 20 of H4) are often preferred sites of methylation, although species-specific differences appear to exist.
- each modified lysine has the capacity to be mono-, di-, or trimethylated, adding yet another level of variation to this posttranslational "mark".
- the present invention is directed to antibodies that are specific for histone H3 and H4 that are methylated at specific lysines. More particularly, one aspect of the present invention is directed to histone H3 lysine 4 and 9. These two lysine residues are found to be methylated in vivo and the methylated forms are associated with euchromatin and heterochromatin, respectively.
- nucleic acid encompasses RNA as well as single and double-stranded DNA and cDNA.
- nucleic acid encompasses RNA as well as single and double-stranded DNA and cDNA.
- nucleic acid encompasses RNA as well as single and double-stranded DNA and cDNA.
- nucleic acid encompasses RNA as well as single and double-stranded DNA and cDNA.
- nucleic acid DNA
- RNA RNA
- similar terms also include nucleic acid analogs, i.e. analogs having other than a phosphodiester backbone.
- peptide nucleic acids which are known in the art and have peptide bonds instead of phosphodiester bonds in the backbone, are considered within the scope of the present invention.
- peptide encompasses a sequence of 3 or more amino acids wherein the amino acids are naturally occurring or synthetic (non-naturally occurring) amino acids.
- Peptide mimetics include peptides having one or more of the following modifications:
- peptides wherein one or more of the peptidyl -C(O)NR ⁇ linkages (bonds) have been replaced by a non-peptidyl linkage such as a ⁇ CH2-carbamate linkage (-CH2OC(O)NR ⁇ ), aphosphonate linkage, a -CH2-sulfonamide (-CH 2 ⁇ S(O)2NR ⁇ ) linkage, a urea ( ⁇ NHC(O)NH ⁇ ) linkage, a -CH2 -secondary amine linkage, or with an alkylated peptidyl linkage (-C(O)NR-) wherein R ⁇ s C1-C4 alkyl;
- a non-peptidyl linkage such as a ⁇ CH2-carbamate linkage (-CH2OC(O)NR ⁇ ), aphosphonate linkage, a -CH2-sulfonamide (-CH 2 ⁇ S(O)2NR ⁇ ) linkage, a urea ( ⁇ NHC(O)
- peptides wherein the N-terminus is derivatized to a --NRR1 group, to a ⁇ NRC(O)R group, to a ⁇ NRC(O)OR group, to a -NRS(O)2R group, to a ⁇ NHC(O)NHR group where R and RI are hydrogen or C1-C4 alkyl with the proviso that R and RI are not both hydrogen; 3. peptides wherein the C terminus is derivatized to ⁇ C(O)R2 where R 2 is selected from the group consisting of C1-C4 alkoxy, and --NR3R4 where R3 and R4 are independently selected from the group consisting of hydrogen and C1-C4 alkyl.
- Naturally occurring amino acid residues in peptides are abbreviated as recommended by the IUPAC-IUB Biochemical Nomenclature Commission as follows: Phenylalanine is Phe or F; Leucine is Leu or L; Isoleucine is He or I; Methionine is Met or M; Norleucine is Nle; Valine is Vat or V; Serine is Ser or S; Proline is Pro or P; Threonine is Thr or T; Alanine is Ala or A; Tyrosine is Tyr or Y; Histidine is His or H; Glutamine is Gin or Q; Asparagine is Asn or N; Lysine is Lys or K; Aspartic Acid is Asp or D; Glutamic Acid is Glu or E; Cysteine is Cys or C; Tryptophan is Tip or W; Arginine is Arg or R; Glycine is Gly or G, and X is any amino acid.
- Other naturally occurring amino acids include, by way of example, 4- hydroxyproline,
- purified and like terms relate to the isolation of a molecule or compound in a form that is substantially free of contaminants normally associated with the molecule or compound in a native or natural environment.
- operably linked refers to a juxtaposition wherein the components are configured so as to perform their usual function.
- control sequences or promoters operably linked to a coding sequence are capable of effecting the expression of the coding sequence.
- the terms “complementary” or “complementarity” are used in reference to polynucleotides (i.e., a sequence of nucleotides) related by the base-pairing rules. For example, for the sequence “A-G-T,” is complementary to the sequence “T-C-A.”
- hybridization is used in reference to the pairing of complementary nucleic acids. Hybridization and the strength of hybridization (i.e., the strength of the association between the nucleic acids) is impacted by such factors as the degree of complementarity between the nucleic acids, stringency of the conditions involved, the length of the formed hybrid, and the G:C ratio within the nucleic acids.
- “Therapeutic agent,” “pharmaceutical agent” or “drug” refers to any therapeutic or prophylactic agent which may be used in the treatment (including the prevention, diagnosis, alleviation, or cure) of a malady, affliction, disease or injury in a patient.
- treating includes alleviating the symptoms associated with a specific disorder or condition and/or preventing or eliminating said symptoms.
- treating cancer includes preventing or slowing the growth and/or division of cancer cells as well as killing cancer cells.
- the term "pharmaceutically acceptable carrier” encompasses any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water and emulsions such as an oil/water or water/oil emulsion, and various types of wetting agents.
- a phosphate buffered saline solution such as a phosphate buffered saline solution, water and emulsions such as an oil/water or water/oil emulsion, and various types of wetting agents.
- antigenic fragment of H3 lysine 4" encompasses both- natural peptide fragments of the amino terminus of Histone 3 (including the peptide fragments of SEQ ID NO: 1,
- the term “antibody” refers to a polyclonal or monoclonal antibody or a binding fragment thereof such as Fab, F(ab')2 and Fv fragments.
- biologically active fragments of the Methyl(K4)H3 or Methyl(K9)H3 antibodies encompasses natural or synthetic portions of the respective full-length antibody that are capable of specific binding to the peptide of SEQ ID NO: 4 or SEQ ID NO: 5, respectively.
- parenteral includes administration subcutaneously, intravenously or intramuscularly.
- K in bold face type (K), when used in the context of an amino acid sequence, will represent a lysine amino acid that has been methylated.
- the present invention is directed to antibodies that bind to specific modifications of the amino terminus of histone H3 and H4 peptides. More particularly, the present invention is directed to the generation of methyllysine- specific histone antibodies. These antibodies recognize lysine residues in histones H3 and H4 that are specifically methylated and may be linked to human biology and disease. Compositions comprising these antibodies are used as diagnostic and screening tools.
- Fig. IA and IB represent immunofluorescence patterns of human metaphase chromosomes from the nonnal female cell line (HH) stained with either the Methyl(K9)H3 antibody (Fig. IA) or the Methyl(K4)H3 antibody (Fig. IB). Localization of the Methyl(K4)H3 and Methyl(K9)H3 antibodies was detected using Cy3 -conjugated secondary antibody (red). Each of the immunofluorescence patterns obtained with the two antibodies revealed one chromosome that is preferentially stained compared to the other chromosomes (indicated by large arrow). As shown in Fig. IB only small regions of the inactive X chromosome are enriched for Lys4 methyl H3 staining.
- the presence of Xist and PGKl promoter DNA sequences in the immunoprecipitated DNA was assayed by PCR.
- the PCR products were separated on 15% polyacrylamide gels, imaged by digital camera, and images were electronically inverted to facilitate visualization of the ethidium bromide-stained bands.
- the Methyl(K4)H3 and Lys9/14 acetyl H3 antibodies preferentially immunoprecipitated the active Xist gene whereas the Methyl(K9)H3 antibody preferentially immunoprecipitated the inactive PGKl gene. From cells containing the active X chromosome, the exact reverse immunoprecipitation pattern was observed.
- Fig. 3 Immunoblot analysis of H3 methylation between simple vs. complex organisms.
- Histones were isolated from various sources, and five ug of total core histones from each species, along with 1 ug of recombinant Xenopus H3 were resolved on a 15% SDS-PAGE, transferred to a PVDF membrane support and probed with either the Methyl(K4)H3 or Methyl(K9)H3 antibody.
- Lanes 1-5 represent histones isolated from recombinant Xenopus H3, budding yeast, Tetrahymena, chicken and the human cell line 293T, respectively. Identical samples were analyzed in parallel and examined by Coomassie staining to monitor histone loading.
- Histone methylation is a poorly understood post-translational modification affecting histones. This modification occurs on selected lysine residues in the amino-terminus of histones. It is now becoming apparent that methylating histone enzymes are involved in both gene activation and repression.
- the present invention is directed to the generation of methyllysine-specific histone antibodies. These antibodies recognize lysine residues in the histones H3 and H4 that are specifically methylated and may be linked to human biology and disease.
- the present invention is directed to post-translational modifications that occur on the flexible N-terminal tails of the core histone proteins H3 and H4. More particularly, the invention is directed to methylated lysine residues.
- methylation of the lysine residues within the first 15 amino acids of the amino terminus of H3 (SEQ ID NO: 7) and H4 (SEQ ID NO: 8) play an important role in the regulation of transcription.
- methylation of lysine 4 (K4) on histone H3 has been associated with transcriptionally active regions of chromatin
- methylation of lysine 9 (K9) on histone H3 has been associated with gene silencing. Therefore, in accordance with one aspect of the present invention methylation of lysine 4 (K4) and lysine 9 (K9) on histone H3 serve as a markers of euchromatin and heterochromatin, respectively, and antibodies recognizing these modified proteins have use as important diagnostic tools.
- the antigen is a purified antigenic fragment of the amino terminus of H3 or H4 methlated at a lysine and selected from the group consisting of ARTKQTARKSTGG (SEQ ID NO: 10), ARTKQTARKSTGG (SEQ ID NO: 11), ARTKQTARKSTGV (SEQ ID NO: 12), ARTKQTARKSTGV (SEQ ID NO: 13), SGRGKGGKGLGKG (SEQ ID NO: 14) and SGRGKGGKGLGKG (SEQ ID NO: 15) or a synthetic equivalent thereof, wherein the bold K represents a methylated lysine residue.
- the antigen comprises an H3 amino terminal fragment of 20 amino acids or less and comprises the sequence ARTKQTAR (SEQ ID NO: 1), QTARKSTGV (SEQ ED NO: 2) or QTARKSTGG (SEQ ID NO: 3), and derivatives of these amino acid sequences wherein the amino acid sequence contains one or more conservative amino acid substitutions.
- the antigen is ARTKQTAR (SEQ ID NO: 1), QTARKSTGV (SEQ ID NO: 2) or QTARKSTGG (SEQ ID NO: 3), or a derivative thereof containing additional non-native amino acids added to either end of the peptide sequence.
- the purified antigen comprises a polypeptide linked to a suitable carrier, such as bovine serum albumin or Keyhole limpet hemocyanin.
- a suitable carrier such as bovine serum albumin or Keyhole limpet hemocyanin.
- the antigen consists of an H3 peptide fragment peptide comprising a sequence selected from the group ARTKQTAR (SEQ ID NO: 1), QTARKSTGV (SEQ ID NO: 2) or QTARKSTGG (SEQ ID NO: 3, and derivatives of this amino acid sequence wherein the amino acid sequence contains one or more conservative amino acid substitutions, and a carrier protein linked to the peptide.
- the antigen may comprise a peptide having the sequence ARTKQTARGC (SEQ ID NO: 4), QTARKSTGVCG (SEQ ID NO: 5), QTARKSTGGCG (SEQ ID NO: 6), AARKSAPVCG (SEQ ID NO: 16), SGGVKKPHKCG (SEQ ID NO: 17) or RHRKILRDCG (SEQ ID NO: 18) wherein the bold K represents the methylated lysine residue and the underlined GC refers to artificial amino acids added to the natural histone sequence.
- the antigen can optionally be linked to a carrier protein.
- the present invention is also directed to antibodies that specifically bind to peptide fragments of the H3 or H4 protein that have been methylated at a lysine residue.
- the antibody will recognize one or more methylated lysine residues present in the first 20 amino acid residues of the amino terminus of the H3 and H4 histones.
- the present invention is directed to an antibody that specifically binds to the peptide ARTKQTARGC (SEQ ID NO: 4), QTARKSTGGCG (SEQ ID NO: 6), QTARKSTGVCG (SEQIDNO: 5), AARKSAPVCG(SEQIDNO: 16),
- the antibody is specific for a peptide comprising the amino acid selected from the group consisting of ARTKQTARGC (SEQ 3D NO: 4), QTARKSTGVCG (SEQ ID NO: 5), QTARKSTGGCG (SEQ ID NO: 6); and amino acid sequences that differ from SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID or SEQ ID NO: 6 by one or more conservative amino acid substitutions.
- the antibody specifically binds to the peptide ARTKQTARGC (SEQ ID NO: 4) or QTARKSTGVCG (SEQ ID NO: 5).
- Antibodies that specifically bind an H3 peptide that is methylated at lysine 4 (i.e. the peptide of SEQ ID NO: 4) will be referred to as Methyl(K4)H3 and antibodies that specifically bind an H3 peptide that is methylated at lysine 9 (i.e. the peptide of SEQ ID NO: 5 or SEQ ID NO: 6) will be referred to as Methyl(K9)H3.
- These two antibodies do not cross react and will not bind to the non-methylated peptide sequences.
- the present invention also encompasses antibodies that bind to the non-methylated histone peptides.
- the antibodies of the present invention are monoclonal antibodies.
- the antibodies or antibody fragments of the present invention can be combined with a carrier or diluent to form a composition.
- the carrier is a pharmaceutically acceptable carrier.
- Such carriers and diluents include sterile liquids such as water and oils, with or without the addition of a surfactant and other pharmaceutically and physiologically acceptable carrier, including adjuvants, excipients or stabilizers.
- Illustrative oils are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, or mineral oil.
- water, saline, aqueous dextrose, and related sugar solution, and glycols such as, propylene glycol or polyethylene glycol, are preferred liquid carriers, particularly for injectable solutions.
- compositions comprising the Methyl(K4)H3 or Methyl(K9)H3 antibody, or bioactive fragments thereof, and a carrier or diluent can be used in conjunction with the method to detect heterochromatin verses euchromatin.
- One method used to generate the antibodies of the present invention involves administration of an antigen, comprising the sequence ARTKQTAR (SEQ ID NO: 1), QTARKSTGV (SEQ ID NO: 2) or QTARKSTGG (SEQ ID NO: 3), to a laboratory animal, typically a rabbit, to trigger production of antibodies specific for the antigen.
- the dose and regiment of antigen administration to trigger antibody production as well as the methods for purification of the antibody are well known to those skilled in the art.
- such antibodies can be raised by administering the antigen of interest subcutaneously to New Zealand white rabbits which have first been bled to obtain pre-immune serum.
- the antigens can be injected at a total volume of 100 ul per site at six different sites.
- Each injected material will contain synthetic surfactant adjuvant pluronic polyols, or pulverized acrylamide gel containing the protein or polypeptide after SDS-polyacrylamide gel electrophoresis.
- the rabbits are then bled two weeks after the first injection and periodically boosted with the same antigen three times every six weeks. A sample of serum is then collected 10 days after each boost. Polyclonal antibodies are then recovered from the serum by affinity chromatography using the corresponding antigen to capture the antibody. Ultimately, the rabbits are euthenized with pentobarbital 150 mg/Kg IV. This and other procedures for raising polyclonal antibodies are disclosed in E. Harlow, et. al., editors, Antibodies: A Laboratory Manual (1988), which is hereby incorporated by reference. The specificity of antibodies may be determined by enzyme-linked immunosorbent assay or immunoblotting, or similar methods known to those skilled in the art.
- the present invention also encompasses monoclonal antibodies that specifically bind to the respective antigen ARTKQTAR (SEQ ID NO: 1), QTARKSTGV (SEQ ID NO: 2) or QTARKSTGG (SEQ ID NO: 3) and their non- methylated counterpart peptides.
- Monoclonal antibody production may be effected using techniques well-known to those skilled in the art. Basically, the process involves first obtaining immune cells (lymphocytes) from the spleen of a mammal (e.g., mouse) which has been previously immunized with the antigen of interest either in vivo or in vitro.
- the antibody-secreting lymphocytes are then fused with myeloma cells or transformed cells, which are capable of replicating indefinitely in cell culture, thereby producing an immortal, immunoglobulin-secreting cell line.
- the resulting fused cells, or hybridomas are cultured, and the resulting colonies screened for the production of the desired monoclonal antibodies. Colonies producing such antibodies are cloned, and grown either in vivo or in vitro to produce large quantities of antibody.
- One embodiment of the invention is directed to a hybridoma cell line which produces monoclonal antibodies which bind the methyl-lysine peptides of the present invention.
- a description of the theoretical basis and practical methodology of fusing such cells is set forth in Kohler and Milstein, Nature, 256:495 (1975), which is hereby incorporated by reference.
- fragments of antibodies can retain binding specificity for a particular antigen.
- Antibody fragments can be generated by several methods, including, but not limited to proteolysis or synthesis using recombinant DNA technology.
- An example of such a embodiment is selective proteolysis of an antibody by papain to generate Fab fragments, or by pepsin to generate a F(ab')2 fragment.
- These antibody fragments can be made by conventional procedures, as described in J. Goding, Monoclonal Antibodies: Principles and Practice, pp. 98-118 (N.Y. Academic Press 1983), which is hereby incorporated by reference.
- Other fragments of the present antibodies which retain the specific binding of the whole antibody can be generated by other means known to those skilled in the art.
- the antibodies are labeled. It is not intended that the present invention be limited to any particular detection system or label.
- the antibody may be labeled with a fluorophore, a radioisotope, or a non-isotopic labeling reagent such as biotin or digoxigenin; antibodies containing biotin may be detected using "detection reagents" such as avidin conjugated to any desirable label such as a fluorochrome.
- the histone specific antibodies of the present invention are detected through the use of a secondary antibody, wherein the secondary antibody is labeled and is specific for the primary (histone specific) antibody.
- the histone specific antibody may be directly labeled with a radioisotope or fluorochrome such as FITC or rhodamine; in such cases secondary detection reagents may not be required for the detection of the labeled probe.
- a method of detecting the presence of methylated lysine residues in the H3 and H4 histones comprises the steps of contacting histone proteins with a labeled antibody, wherein the antibody specifically binds only to H3 that is methylated at lysine 4 or H3 methylated at lysine 9.
- the antibodies of the present invention are labeled for use in diagnostic imaging.
- labels useful for diagnostic imaging in accordance with the present invention are radiolabels such as 13 l ⁇ , 11 ljii, 123 ⁇ 5 99m ⁇ c , 32 P? 125 ⁇ 5 3H, 1 C, and 1 8 8Rh, fluorescent labels such as fluorescein and rhodamine, nuclear magnetic resonance active labels, electron dense or radiopaque materials, positron emitting isotopes detectable by a positron emission tomography (“PET”) scanner, chemilluminescers such as luciferin, and enzymatic markers such as peroxidase or phosphatase.
- PET positron emission tomography
- Short-range radiation emitters such as isotopes detectable by short-range detector probes, such as a transrectal probe
- short-range detector probes such as a transrectal probe
- isotopes and transrectal detector probes when used in combination, are especially useful in detecting prostatic fossa recurrences and pelvic nodal disease.
- the antibodies of the present invention can be labeled with such reagents using techniques known in the art. For example, see Wensel and Meares, Radioimmunoimaging and Radioimmunotherapy, Elsevier, New York (1983), which is hereby incorporated by reference, for techniques relating to the radiolabeling of antibodies. See also, D.
- the antibody is labeled with a fluorophore or chromophore using standard moieties known in the art.
- methylation of histone H3 at lysines 4 and 9 correlates, respectively, with activation and inactivation of expression of genes in proximity to the modified histones.
- Histone H3 when methylated at K9 is a preferred binding site for the heterochromatin protein HP 1 , which in turn can recruit the enzyme Suv39h responsible for K9 methylation, creating a mechanism by which the inactivation signal can be propagated.
- Methylation of K9 also precludes acetylation at that site, further contributing to repression.
- methylation at histone H3 K4 is correlated with transcriptional activity.
- antibodies specific for the K4 methylated histone H3 can be used to detect transcriptionally active regions of chromatin and antibodies specific for K9 methylated histone H3 transcriptionally can be used to detect inactive regions of chromatin.
- in situ staining of chromosomes reveals that the staining patterns generated by the Methyl(K4)H3 and Methyl(K9)H3 antibodies produce mirror images of one another.
- Methyl(K4)H3. and Methyl(K9)H3 antibodies have the potential for use in humans as diagnostic and therapeutic agents
- one embodiment of the present invention is directed to humanized versions of the Methyl(K4)H3 and Methyl(K9)H3 antibodies.
- Humanized versions of the antibodies are needed for therapeutic applications because antibodies from non-human species may be recognized as foreign substances by the human immune system and neutralized such that they are less useful.
- Humanized antibodies are immunoglobulin molecules comprising a human and non-human portion. More specifically, the antigen combining region (variable region) of a humanized antibody is derived from a non- human source (e.g. murine) and the constant region of the humanized antibody is derived from a human source.
- the humanized antibody should have the antigen binding specificity of the non-human antibody molecule and the effector function conferred by the human antibody molecule.
- creation of a humanized antibody involves the use of recombinant DNA techniques.
- The- antibodies of the present invention can also be linked to an insoluble support to provide a means of isolating euchromatin or heterochromatin from cells.
- the support may be in particulate or solid form and could include, but is not limited to: a plate, a test tube, beads, a- ball, a filter or a membrane. Methods for fixing antibodies to insoluble supports are known to those skilled in the art. In one embodiment an antibody of the current invention is fixed to an insoluble support that is suitable for use in affinity chromatography.
- Methyl(K4)H3 and Methyl(K9)H3 antibodies are large-scale or domain-sensitive chromatin marks that are somehow set up by boundary elements.
- chromatin that is associated with histones that include H3 methylated at Lsy4 represent an "on" domain, or at least a domain that is competent for transcriptional activity.
- chromatin that is associated with histones that include H3 methylated at Lsy9 represent an "off" domain, that is not competent for transcriptional activity. This pattern is conserved across a diverse range of species.
- Zoo blots with these antibodies suggest that most of the H3 histones from 'simple' organisms (budding yeast) and Tetrahymena, contain a methylated Lys4 (ON), whereas in striking contrast, most of the H3 histones present in 'complex' organisms have a methylated Lys9 (OFF) (see Fig. 3).
- the 'default' or ground state in more complex eukaryotes is OFF. Knowing how to identify ON chromatin through use of the Lys4 methyl mark may prove invaluable in developing strategies for better targeting of transgene to more 'friendly' chromatin.
- Chromatin immunoprecipitation data supports the above 'ON/OFF' marking system model.
- S. pombe chromatin IP data published (Science Nakayama et al., 2001) and the work on the inactive X chromosome in humans (see Example 2) supports this model.
- a method for detecting chromatin alterations that are associated with a disease state.
- the term "disease state” is intended to encompass any condition that is associated with an impairment of the normal state of a living animal or plant including congenital defects, pathological conditions such as cancer, and responses to environmental factors and infectious agents (bacterial, viral, etc.).
- the method comprises the steps of isolating chromatin from both normal and diseased tissue, contacting the two pools of chromatin with either the Methyl(K4)H3 or
- Methyl(K9)H3 antibody and comparing the staining pattern of the chromatin isolated from normal tissue to that of the diseased tissue. Furthermore, using chromatin immunoprecipitation, unique tumor suppressor genes could be isolation by differential screening using the antibodies of the present invention.
- the present invention the
- Methyl(K4)H3 and Methyl(K9)H3 antibodies are used to identify heterochromatin and euchromatin regions and thus detect transcriptionally active and inactive regions of chromatin. More particularly, the antibodies can be used to detect changes in chromatin structure that are associated with a given disease state. Therefore the antibodies can be used as a diagnostic to detect alterations of chromatin structure that are associated alterations in expression patterns (i.e. differences in heterochromatin vs euchromatin patterns relative to predominant native patterns). Alterations in chromatin structure for a specific region of chromatin may be diagnostic of a particular disease state.
- conversion of a normally euchromatic region of the genome to heterochromatin may represent the suppression of a tumor suppressor gene that is indicative of cancer or a pre-cancer state.
- conversion of a region of heterochromatin to euchromatin may be associated with the inappropriate or overexpression of a gene that has deleterious effects on the host cell/organism.
- the present invention is also directed to a method of using broad-based differential screening techniques to isolate nucleic acid regions that have altered expression patterns in diseased tissues.
- chromatin can be isolated from diseased tissues and compared to chromatin isolated from healthy tissues to determine if there are any differences in the chromatin structure (i.e. changes in heterochromatin vs. euchromatin) that are associated with the disease state.
- differences in chromatin structure may represent suppression or overexpression of genes that play a direct or indirect role in the disease.
- the anti-methyl(Lys 9) H3 and anti-methyl(Lys 4) H3 antibodies can be used to detect such changes in chromatin structure and help identify genes that are associated with the disease state. The identification of such genes will assist in designing more effective therapies for treating the disease.
- the method for detecting alterations in chromatin structure associated with a particular disease comprises chromatin immimoprecipitation assays, using modification-specific histone antobodies. This process allows for the analysis of a wide range of DNA-templated processes that are governed by the chromatin environment.
- the method comprises the steps of isolating chromatin from both diseased tissue and healthy tissue, fragmenting the DNA (preferably by sonification), and immunoprecipitating chromatin using an antibody that specifically binds to the amino acid sequence of ARTKQTAR (SEQ ID NO: 1) or QTARKSTGV (SEQ ID NO: 2), wherein the bold K represents a methylated lysine residue, and comparing the chromatin (and the associated DNA sequences) immunoprecipitated from the healthy tissue relative to the diseased tissue. Comparison of the two pools of immunoprecipitated chromatin will allow for the identification of differences between diseased and healthy tissues.
- comparison of the two pools of immunoprecipitated chromatin comprises the steps of isolating the nucleic acid sequences associated with the two pools of immunoprecipitated chromatin and comparing the resulting two pools of nucleic acid sequences. Comparison of the two pools of nucleic acid sequences can be conducted using any of the standard molecular techniques, including PCR, gel electrophoresis, nucleic acid sequencing and nucleic acid hybridization analysis. Those nucleic acid sequences that are present in only one of the two pools of nucleic acid sequences are then recovered. These nucleic acid sequences represent expressed suppressed genes that are associated with either the normal or diseased tissue.
- the antibodies used to immunoprecipitate the chromatin are selected from the group consisting of Methyl(K4)H3 and Methyl(K9)H3 antibody.
- chromatin IP chromatin immunoprecipitation
- DNA immunoprecipitated using the Methyl(K4)H3 antibody can be immobilized on a solid surface or "chip” and thus represent all the nucleic acid sequences of a given cell that is competent for transcription.
- DNA immunoprecipitated using the Methyl(K9)H3 antibody can be immobilized on a solid surface or "chip” and thus represent all the nucleic acid sequences of a given cell that is not competent for transcription.
- Harvesting mRNA or preparing cDNA from a target cell, labeling the target nucleic acids and then hybridizing the target DNA with the immobilized DNA will reveal abnormal expression of genes. Knowing this information may prove invaluable in determining the on/off state of key tumor suppressor or oncogenic proteins in various human cancers.
- immunoprecipitation of chromatin will be used to map the location of active genes at a genome- wide level through the use of microarrays.
- the method of comparing the two pools of immunoprecipitated chromatin comprises the use of a gene chip, DNA microarray, or a proteomics chip using standard techniques known to those skilled in the art.
- the chip will contain an ordered array of known compounds, such as known DNA sequences, so that interaction of the immunoprecipitated chromatin at a specific location of the chip will identify, and allow for the isolation of, DNA sequences associated with the immunoprecipitated chromatin.
- H3 lysine 27 AARKSAPVCG (SEQ ID NO: 16)
- H3 lysine 36 SGGVKKPHKCG (SEQ ID NO: 17)
- H4 lysine 20 RHRKILRDCG (SEQ ID NO: 18) wherein the bold K is the methylated lysine residue and underlined GC refers to artificial amino acids added to the H3 sequence to aid in the production of this antibody.
- the antibodies of the present invention can be used in standard Molecular Biology techniques such as Western blot analyses, immunofluorescence, and immunoprecipitation. As noted above the presence of methylated H3 at lysine 4 correlates with transcriptionally active nuclei, and therefore, this H3 antibody may be a useful in the understanding of gene regulation. In addition it is anticipated that microinjection of the Methyl(K4)H3 antibody into cells may interfere with the activation of specific genes.
- a kit for detecting euchromatin and heterochromatin.
- the kit comprises an antibody that specifically binds to a lysine methlyated modified peptide selected from the group consisting of ARTKQTARGC (SEQ ID NO: 4), QTARKSTGVCG (SEQ ID NO: 5), ARTKQTAR (SEQ ID NO: 1), QTARSTGV (SEQ ID NO: 2), ARTKQTARKSTGV (SEQ ID NO: 9), AARKSAPVCG (SEQ ID NO: 16), SGGVKKPHKCG (SEQ ID NO: 17) and RHRKILRDCG (SEQ ID NO: 18).
- ARTKQTARGC SEQ ID NO: 4
- QTARKSTGVCG SEQ ID NO: 5
- ARTKQTAR SEQ ID NO: 1
- QTARSTGV SEQ ID NO: 2
- ARTKQTARKSTGV SEQ ID NO: 9
- AARKSAPVCG SEQ ID NO: 16
- the kit comprises an antibody that binds to the peptide ARTKQTARGC (SEQ ID NO: 4), QTARKSTGVCG (SEQ ID NO: 5) or QTARKSTGGCG (SEQ ID NO: 6), wherein the bold K represents a methylated lysine residue.
- the antibodies are attached to an insoluble support, wherein the support is either a monolithic solid or is in particular form.
- the antibodies are monoclonal antibodies and in a further embodiment the antibodies are labeled.
- the antibodies of the present invention can be packaged in a variety of containers, e.g. , vials, tubes, microtiter well plates, bottles, and the like. Other reagents can be included in separate containers and provided with the kit; e.g., positive control samples, negative control samples, buffers, cell culture media, etc.
- kits for use in an assay to determine if a sample has methylase activity.
- the kit comprises a peptide selected from the group consisting of ARTKQTARGC (SEQ ID NO: 4),
- QTARKSTGVCG (SEQ ID NO: 5), ARTKQTAR (SEQ ID NO: 1), QTARSTGV (SEQ ID NO: 2) and ARTKQTARKSTGV (SEQ ID NO: 9) and an antibody that specifically binds to a lysine methlyated modified peptide selected from the group consisting of ARTKQTARGC (SEQ ID NO: 4), QTARKSTGVCG (SEQ ID NO: 5), ARTKQTAR (SEQ ID NO: 1), QTARSTGV (SEQ ID NO: 2) and
- ARTKQTARKSTGV SEQ ID NO: 9
- the antibodies are attached to an insoluble support, wherein the support is either a monolithic solid or is in particular form.
- the kit is fiirther provided with an antibody that specifically binds to a non-methylated peptide selected from the group consisting of ARTKQTARGC (SEQ ID NO: 4), QTARKSTGVCG (SEQ ID NO: 5), ARTKQTAR (SEQ ID NO: 1), QTARSTGV (SEQ ID NO: 2) and ARTKQTARKSTGV (SEQ ID NO: 9).
- ARTKQTARGC SEQ ID NO: 4
- QTARKSTGVCG SEQ ID NO: 5
- ARTKQTAR SEQ ID NO: 1
- QTARSTGV SEQ ID NO: 2
- ARTKQTARKSTGV SEQ ID NO: 9
- the method for detecting the methylase activity of a sample comprises contacting a peptide selected from the group consisting of
- ARTKQTARGC SEQ IDNO: 4
- QTARKSTGVCG SEQ IDNO: 5
- ARTKQTAR SEQ IDNO: 1
- QTARSTGV SEQIDNO: 2
- ARTKQTARKSTGV SEQ ID NO: 9
- the amount of methylation-specific antibody i.e. Methyl(K4)H3 or Methyl(K9)H3
- This assay can also be used to screen for potential inhibitors of a methylase.
- a method of screening for inhibitors of arginine methyl transfer activity comprises the steps of providing a sample, wherein the sample comprises a methylase and a substrate that is methylated by said methylase, adding a potential inhibitor of the methylase to the sample, and contacting the sample with an antibody that binds specifically to the methylated substrate, but not the non-methylated substrate.
- the antibody is specific for the peptide ARTKQTAR (SEQ ID NO: 1) or QTARKSTGV (SEQ ID NO: 2). Quantifying the amount of antibody bound to the peptide is a direct correlation of the level activity of the methylase in the sample.
- the methylase activity to be detected is SuVar3-9 (for Lys 9) or Setl (for Lys 4).
- 'Knock-out' strains are available for all of the non-essential genes present in budding yeast...around 4,800.
- the antibodies of the present invention have such a high degree of specificity, that they only detect one or two major bands in yeast whole cell lysates, thus allowing for the development of a robotic screening method to look at all of these knock-out strains.
- Using Lys4 methyl H3 should lead to the entire upstream pathway of 'regulators' including the on and off enzymes (provided the gene product is non-essential).
- Setl is the enzyme responsible for the Lys4 H3 methyl mark in yeast, and is also one of the Lys4 HMTases in humans.
- Lys4 methylation was discovered to be regulated by H2B ubiquitination at a conserved Lysine on the opposite side of the nucleosome. This is the first example of a 'trans-tail' effect meaning that one histone modification on one tail effect another modification on another not-so-close tail.
- HR6 human Rad6
- HR6A and HR6B Mice knockouts of HR6B -/- are male sterile in a pathway that is not known, but seems to lead to chromatin defects during spermatogenesis leading to sperm death. Accordingly it is anticipated that HR6B is responsible for ubiquitin addition on H2B and therefore it is possible that Lys4 H3 methyl antibodies will be a diagnostic for male infertility. Furthermore, the possibility exists that defects in Lys9 methylation could impact X-inactivation and lead to female infertility.
- the Methyl(K4)H3 and Methyl(K9)H3 antibodies are used as a diagnostic to screen for male and female infertility defects.
- Current models suggest that Lys9 methylation is catalzyed, at least in some instances by SuVar3 -9. It appears that the Lys9 methyl mark is read by chromodomains, short protein modules that act as chromatin 'velcro' patches. Best documented is the chromodomain of the heterochromatin protein HP1. Interestingly, the chromodomain from HP1, binds well to Lys9 methyl H3 peptides, but binds much less well to Lys4 or unmodified peptides. It is interesting also that SuVar3-9 itself, a catalytic HMTase, also has a chromodomain, a module whose site specificity for methylated histone peptides has yet to be tested.
- the uniquely-modified peptides of the present invention including ARTKQTAR (SEQ ID NO: 1) or QTARKSTGV (SEQ ID NO: 2) are used as affinity reagents to look for polypeptides that bind Lys4 H3 peptides.
- ARTKQTAR SEQ ID NO: 1
- QTARKSTGV SEQ ID NO: 2
- HATs histone acetyltransferases
- Esal and CDY both of whom have chromodomains.
- CDY is a testis-specific HAT encoded on the male Y chromosomes, and somatic histones are well known to be hyperacetylated during a reaction that leads to replacement by protamines.
- Somatic histones are displaced, followed by transition proteins, followed by protamines
- Antibodies to ubiquitinated H2B and H2A, Lys4 methyl H3 and sites of CDY- catalyzed acetylation would all be of potential diagnostic value in male infertility screens.
- a short polypeptide corresponding to the amino-acid sequence of histone H3 surrounding lysine 4 (SEQ ID NO: 4; ARTKQTARGC) or lysine 9 (SEQ ID NO: 5; QTARKSTGVCG) was first chemically synthesized, wherein the bold K is the methylated lysine residue and underlined GC refers to artificial amino acids added to the H3 sequence to aid in the production of this antibody.
- This polypeptide was then conjugated to cationized bovine serum albumin (BSA), and the conjugated-peptide was injected into rabbits.
- BSA bovine serum albumin
- Histones H3 and H4 are largely hypoacetylated in heterochromatic chromosomal regions in organisms as diverse as yeast, flies, and mammals. In fission yeast, hypoacetylation of histones is associated with the silent mating-type region and centromeres, chromosomal domains that share many parallels with heterochromatic regions in higher eukaryotes. Centromeric regions comprising a central core of unique sequences surrounded by inner (imr) and outer (otr) repeats are assembled into silenced chromatin structures.
- Clr3 and Clr6 belong to family of histone deacetylases (HDACs). Swi6 and Clr4 proteins contain a chromodomain, an evolutionarily conserved motif initially identified in HP1 and Polycomb proteins.
- Clr4 preferentially methylated the H3 1-20 unmodified peptide but failed to methylate the H3 19-35 unmodified peptide, indicating that the target residue of Clr4 HMTase resides in the first 20 amino acids of H3.
- mutations in the chromo-domain [Tip 31 to Gly (W31G) and Tip 41 to Gly (W41G)] had little effect on Clr4 HMTase activity
- mutations in the SET domain [Gly 328 to Ser (G378S)] and both cysteine-rich regions [Arg 320 to His (R320H) and Gly 486 to Asp (G486D)] greatly reduced Clr4 HMTase activity, indicating that these three regions are critical for Clr4 HMTase activity in vitro.
- H3 Lys 9 -methyl specific antibody was developed.
- the H3 Lys 9 -methyl antibody specifically recognized the H3 1-20 Lys 9 -methyl peptide in a wide range of antibody dilution.
- the H3 Lys 9 -methyl antibody did not detect recombinant histone H3 (rH3) alone compared with the HeLa core histone positive control but did detect rH3 selectively methylated by rClr4, further demonstrating the specificity of this antibody (see Nakayama et al., (2001) Science, 292, pp 110-113; the disclosure of which is incorporated herein).
- H3 Lys 9 -methyl modification is specifically localized at the silenced chromosomal regions.
- H3 Lys 9 methylation and Swi6 were preferentially enriched at a marker gene (Kint2::ura4 1 ) inserted within the silenced mat2 ⁇ chromosomal domain, compared with control ura4DS/E locus at the endogenous location.
- H3 Lys 9 methylation was also preferentially enriched at the ura4 1 marker inserted within the highly repressed innermost repeat (imrlR::ura4 1 ) and the outer repeat (otrlR::ura4 1 ), but not at the weakly repressed central core (cntl::ura4 1 )ofcenl.
- H3 Lys 9 methylation coincided with the presence of Swi6 at these regions (Partridge et al, (2000), Genes Dev., 14, 783).
- H3 Lys 9 is the physiological target of Clr4 HMTase activity and that Clr4 appears to be the exclusive in vivo H3 Lys 9 -specific HMTase at mat and cen loci.
- WD-40 proteins are involved in many aspects of chromatin remodeling and histone metabolism, such as chromatin assembly and acetylation or deacetylation of histones. Therefore, the b-propeller domains of Rikl may form a complex with Clr4 to recruit its HMTase activity to heterochromatic regions and may play a role in coupling other transacting factors, such as Swi6 and histone deacetylases.
- Swi6 The possible role of Swi6 on Clr4-dependent methylation of H3 Lys 9 was also tested. Strains carrying swi ⁇ -115 (W269R) mutation that severely reduced Swi6 protein levels were used. As expected, Swi6 localization at both mat and cen was abolished as demonstrated by ChIP analysis. The swi6-115 mutation did not cause any detectable change in H3 Lys 9 methylation when compared with the wild- type strain. These data indicate that Swi6 is dispensable for Clr4 function and suggest that Swi6 acts down-stream of Clr4 H3 Lys 9 methylation.
- HDACs and HMTases act cooperatively to establish a "histone code" that is then recognized by Swi6. More specifically, the HDACs (Clr6 and/or Hdal) deacetylate H3 Lys 9, whereas Clr3 deacetylates H3 Lys 14 before H3 Lys 9 methylation by the Clr4/Rikl HMTase complex. Swi6 binding to the H3 Lys 9 -methyl modification would then result in self-propagating heterochromatin assembly. Because the heterochromatin-binding domain of Swi6 was mapped to its chromodomain, it is most likely that this protein motif has evolved to recognize the H3 Lys 9 -methyl modification.
- Swi6 remains associated with the mat2/3 region throughout the cell cycle where it acts as an important determinant of the epigenetic cellular memory, promoting inheritance of the silenced state. Because the mouse homolog of Swi6, M31, associates with Su(var)3-9, a similar inter-action between Clr4 and Swi6 is predicted. The close association of Clr4 enzymatic HMTase activity, followed by recruitment and binding of Swi6 to Lys 9 methyl "marks" in H3 through its chromodomain, suggests a pathway of epigenetic inheritance.
- Chromosomes in higher eukaryotes have historically been considered to consist of regions of euchromatin and heterochromatin, which are distinguished by the degree of condensation and level of transcriptional activity of the underlying DNA sequences. Certain regions of constitutive heterochromatin are found at or near specialized structures such as centromeres, and are comprised mostly of genetically inert repetitive sequences. In contrast, other regions that have the same primary DNA sequences can exhibit characteristics of either type of chromatin, suggesting that epigenetic factors, such as packaging of DNA by histones and chromatin-associated proteins, dictate the heterochromatin status at these loci.
- X chromosome inactivation seen in female cells of mammals. This process allows for dosage compensation of X-linked genes whereby one of the two copies of the X chromosome in female cells is randomly inactivated during embryonic development. Current evidence suggests that X inactivation is initiated by the up-regulation of the non-coding XIST transcript and its association in cis with the chromosome to be inactivated.
- the inactive X chromosome acquires heterochromatic characteristics such as late replication timing, a condensed appearance (Barr body) in interphase cells, DNA methylation of CpG islands at house-keeping genes, and association with altered nucleosomes that are composed of hypoacetylated histones and enriched for the H2A variant MacroH2A. While the exact roles of these properties in the onset of X inactivation remain unclear, once the inactive state has been established, these epigenetic characteristics seem to act synergistically to maintain the remarkable stability of the inactive X through many cell divisions in the adult soma.
- the inactive X was investigated for enrichment for Lys9-methylated H3.
- HH normal lymphoblast cell line
- a normal human female lymphoblast cell line (HH) and a female lymphoblast cell line which contains five X chromosomes (606 IB) were grown, harvested and collected onto microscope slides with a Cytospin 3 centrifuge.
- Modified histones were detected by indirect immunofluorescence, essentially as described in detail elsewhere (Costanzi and J. R. Pehrson, Nature 393, 599 (1998)). Briefly, cells were incubated for one hour at 37 °C in a humid chamber with serial dilutions of the primary Lys9 methyl H3 or acetyl H4 antisera and washed in KCM (120mM KC1, 20mM NaCl 10 mM TRIS-CL, pH 8.0, 0.5 M EDTA, 0.1% Triton). The cells were then incubated for 30 min at room temperature with Cy3- conjugated, affinity-purified, donkey anti-rabbit IgG antibody (Jackson ImmunoResearch) diluted 1 :40 in KCM.
- chromosomes were counterstained with 4',6-diamidino-2-phenylindole (DAPI), mounted in antifade (Vectashield) and viewed on a Zeiss Axiophot fluorescence microscope.
- DAPI 4',6-diamidino-2-phenylindole
- lysine 4 of H3 is another documented site of methylation.
- lysine 9 lysine 4 methylation has been correlated with active transcription.
- metaphase chromosomes were stained using an antibody specific for Lys4-methylated H3.
- Metaphase chromosomes from female cell lines HH and 606 IB were incubated with Lys4 methyl H3 antiserum and the staining pattern was analyzed by indirect immunofluorescence as described earlier.
- this antibody intensely stains all chromosomes in the metaphase spread except for a single chromosome per spread (Fig. IB).
- This unique chromosome is almost totally devoid of staining except for several 'hot spots' of H3 lysine 4 methylation.
- Staining of the metaphase spreads of the 5X cell line shows that four of the chromosomes are understained using the Lys4 methyl H3 antibody, suggesting that the hypo-H3 Lys4- methylated-chromosome(s) is the inactive X chromosome. Closer examination of the inactive X chromosome shows that there are several distinct regions of this chromosome that exhibit intense staining with the Lys4 methyl H3 antibody.
- Lys4 methyl H3 staining on the inactive X correspond to the location of multiple genes known to escape inactivation (Carrel et al, Proc NatlAcad Sci USA 96, 14440 (1999)), and these data are therefore consistent with the idea that Lys4 methylation of H3 is associated with active gene expression.
- the understaining of the inactive X chromosome by the Lys4 methyl H3 antibody is similar, but not identical, to the staining pattern of this chromosome with antibodies against hyperacetylated form of H4.
- some staining at the telomeric region of the p arm of the inactive X chromosome was seen using the antibody against hyperacetylated H4, but not at the Xpl 1 and Xq25-26 regions.
- previously published results showed that three regions on the inactive X chromosome (Xpter-22.2, Xpl 1.3-11.2, and Xq22) were stained with an antibody against hyperacetylated H4, but this was seen only in sodium butyrate-treated human cells.
- IMR 90 ATCC cells were grown on coverslips for 24-48 hours then fixed in 4% formalehyde for 15 minutes at room temperature; the cells were then permeabilised in PBS containing 0.5% Triton-X for 4 min. on ice, washed in PBS and then washed in 2xSSC prior to RNA FISH. To preserve nuclear structures, cells were kept continously hydrated.
- RNA FISH hybridization and washes were performed essentially as described elsewhere (Lachner et al, Nature 410, 116 (2001)). Briefly, cells were hybridized with a XIST probe comprising a pool of four exon-derived DNA fragments spanning a total of 4.5 kb of sequence, labeled by nick translation with Spectrum Red or Green dUTP (Vysis, Downer Grove, EL). Following hybridization overnight at 37°C, standard washes for RNA FISH (ie 3x in 50% formamide / 2xSSC and 3x in 2xSSC) were performed. The cells were then washed in PBS / 0.5% BSA prior to performing immunofluorescence.
- the XIST transcript specifically localizes to the inactive X chromosome at interphase but not at metaphase, and localization of the Xist transcript can be detected by FISH analysis.
- the Lys9-methyl-H3 antibody preferentially stains a region that is heterochromatin-dense as indicated by co- localization with DAPI-dense regions. This condensed region also co-localizes with the XIST RNA signal, indicating that the chromosome enriched for Lys9-methylated H3 is indeed the inactive X.
- Lys4 and Lys9 methyl H3 antibodies would respectively enrich for active and inactive genes on the X chromosome by chromatin immunoprecipitation (ChIP).
- ChIP chromatin immunoprecipitation
- the XIST gene is transcriptionally active whereas the PGKl gene is silenced.
- the XIST gene is silent whereas the PGKl gene is actively transcribed.
- two CHO somatic hybrid cell lines were used that contain either a single active or inactive human X chromosome in ChIP assays in order to examine the histone modifications associated with genes present on the active or inactive X chromosomes.
- Chromatin from these two cell lines were immunoprecipitated using antibodies against Lys9- methylated H3, Lys4-methylated H3, or Lys9/14-acetylated H3, and the immunoprecipitated DNA was PCR amplified using primers specific to the promoter regions of the human Xist and PGKl genes.
- Chromatin immunoprecipitation assays were done as described in Cheung et al, Mol Cell 5, 905 (2000).
- formaldehyde-fixed chromatin was harvested from CHO somatic cell hybrids containing either the active or inactive human X chromosome.
- Approximately 3 x 10 6 cells- worth of sonicated chromatin were used per immunoprecipitation reaction with the antibodies indicated in the text.
- the immunoprecipitated DNA was analyzed by PCR using primers specific for the promoter regions of the human XIST and PGKl genes (primer sequences and PCR conditions were derived from Gilbert and P. A. Sharp, Proc NatlAcadSci USA 96, 13825 (1999)), and analyzed by polyacrylamide gel electrophoresis.
- the acetylated H3 antibody immunoprecipitated XIST DNA only from the inactive X chromosome, and the PGKl DNA only from the active chromosome.
- the Lys4 methyl H3 antibody preferentially immunoprecipitated the _ ⁇ STDNA from the cells actively expressing XIST (from the cells containing the inactive X chromosome) and the PGKl DNA from the cells containing the active X chromosome. Therefore, both acetylated H3 and Lys4-methylated H3 are enriched at the actively transcribing loci on both the active and inactive X chromosomes.
- Immunoprecipitation using the Lys9 methyl H3 antibody showed reciprocal results to those obtained with the Lys4 methyl and acetyl H3 antibodies.
- XIST DNA was immunoprecipitated only from cells containing the active X chromosome whereas the PGKl DNA was immunoprecipitated only from the inactive X chromosome.
- the inactive X chromosomes is a well-studied paradigm for epigenetic regulation of gene expression and for linking specialized nucleosomal architecture with transcription silencing.
- the entire inactive X chromosome seems to be largely devoid of hyperacetylated histones, and a core histone variant, MacroH2A, has been found to be enriched at the inactive X chromosome.
- MacroH2A a core histone variant
- none of the above modifications alone can account for the stability associated with this form of epigenetic regulation.
- Histone methylation however, has recently been described as a more 'stable' epigenetic chromatin mark whose functions in X inactivation and as a potential cellular 'memory' marker have yet to be explored.
- methylation of histone H3 at lysine 9 has been defined to be an important modification for heterochromatin assembly, and as shown here, this modification is also enriched in the facultative heterochromatin of the inactive X chromosome.
- methylation of ⁇ 3 at lysine 4 is complementarily absent in the inactive X chromosome, suggesting that methylation of H3 at these two distinct sites may be reciprocal, and that H3 molecules methylated at lysine 4 are preferentially associated with transcriptionally active genes whereas the opposite is true for H3 methylated at lysine 9.
- H3 methylated at lysine 9 functioning to recruit chromatin-binding factors
- H3 methylated at lysine 4 may function to recruit transcription-enhancing factors or to block the association of transcription-repressive factors; however, direct evidence for either of these possibilities is still lacking.
- the present ChIP assays only examined promoters of X-linked genes, but it is anticipated that H3. methylated at these two respective sites are genome-wide marks that demarcate chromosome domains.
- methylation of H3 at lysines 4 or 9 may dictate the spatial distribution of associated chromosome regions in transcriptionally permissive versus restrictive environment.
- Imprinted genetic loci show differential expression of maternal compared to paternal alleles in some or all tissues at some or all stages of development.
- the functional differences between maternal and paternal alleles of imprinted genetic loci must reflect structural differences between maternal and paternal chromosomes in the regions containing these loci.
- the simplest models for establishment of these structural differences hold that chromosomal domains are marked differentially during oogenesis and spermatogenesis, and that these gametic imprinting marks are maintained after fertilization in somatic cells.
- the gametic imprinting marks are identical to the imprinting marks responsible for differential gene expression after fertilization. If the gametic marks are not the same as the somatic marks, there must be a mechanism for reading the gametic marks and using their information to impose somatic imprinting marks.
- the identity of the imprinting marks in mammals has been the subject of extensive speculation and experimental analysis.
- An appealing candidate imprinting mark is 5-methylcytosine in CpG dinucleotides.
- Many imprinted loci show parent-of-origin specific DNA methylation of imprinted regions, and some of these parent-specific DNA methylation marks are established during gametogenesis and maintained in somatic cells.
- DNMTs maintenance DNA methyltransferases
- the promoter region of the imprinted SNRPN-gene in the Prader-Willi syndrome (PWS) imprinting center shows differential cytosine methylation in somatic tissues of mouse and human, and the region is heavily methylated in mouse oocytes but unmethylated in mouse sperm; however, El-Maarri et al. (Nature Genet. 27, 341 (2001)) have recently shown that this region is completely unmethylated in human oocytes, as in human sperm, so that the differential cytosine methylation must arise after fertilization.
- this structural difference might be a heritable covalent modification of DNA other than cytosine methylation, a DNA-associated protein that remains stably associated with either the maternal or the paternal chromosome from the gamete through somatic cell divisions, or a covalent modification of a DNA-associated protein that is inherited in a parent-specific fashion.
- Histone modifications especially acetylation, have previously been shown to mediate effects of a number of transcriptional regulatory proteins, presumably by changing chromatin structure to increase accessibility to other transcriptional factors.
- acetylated histones which are quite labile
- methyl groups attached to histones show a very low level of turnover, making histone methylation a good candidate modification in epigenetic processes such as imprinting.
- a histone modification that has recently been associated with the formation of stable silenced chromatin regions in Drosophila and fission yeast, (the methylation of histone H3 on Lys9) as been examined along with the methylation of histone H3 on Lys4, which has been correlated with transcriptional activity in Tetrahymena.
- the Prader-Willi syndrome (PWS)/Angelman syndrome (AS) region in human chromosome 15ql l-ql3 contains at least 10 imprinted genes within a ⁇ 2 Mb region (Nicholls et al, Trends Genet. 14, 194 (1998)); 8 of these genes are expressed exclusively from the paternal chromosome, and loss of the active paternal alleles of these genes causes PWS, characterized by infantile hypotonia, mild developmental delay, and later-onset hyperphagia and obesity. Loss of the active maternal allele of one gene in this region, UBE3 A, causes AS, characterized by severe mental retardation, lack of speech, seizures, and easily provoked laughter.
- This region can exist in either of two mutually exclusive epigenetic states, the paternal state and the maternal state.
- Establishment of the paternal state requires a DNA segment, referred to as the PWS imprinting center (PWS-IC) that includes the SNRPN promoter in cis; establishment of the maternal state requires a DNA segment approximately 30 kb centromeric of the PWS-IC referred to as the AS-IC.
- PWS-IC PWS imprinting center
- AS-IC DNA segment approximately 30 kb centromeric of the PWS-IC referred to as the AS-IC.
- Chromatin prepared from stimulated lymphocytes of controls, PWS individuals (lacking a paternal copy of 15ql l-ql3 through deletion or imprinting defect), and AS individuals (lacking a maternal copy of 15ql l-ql3) was immunoprecipitated with antibodies specific for either H3 methylated on Lys9 or H3 methylated on Lys4. DNA recovered from the immunoprecipitation was assayed by PCR for sequences in the PWS-IC, including the SNRPN promoter, and for other sequences in the region.
- the maternal copy of the PWS imprinting center (present in PWS chromatin) was immunoprecipitated by anti-methyl Lys9 H3 antibody, while there was dramatically reduced precipitation of this sequence on the paternal copy (present in AS chromatin).
- This result correlates well ' with the observation that maintenance of silenced heterochromatin in both Drosophila and fission yeast requires the function of Lys9 histone H3 methyltransferases.
- the region of maternal- specific H3 Lys9 methylation extends approximately 0.6 kb 5' and 0.5 kb 3'from the SNRPN promoter.
- the paternal copy of the PWS-IC was immunoprecipitated by anti-methyl Lys4 H3 antibody. This sequence was not precipitated on the maternal copy. Previous reports of association of this modification with active chromatin are consistent with these findings.
- methyl Lys9 H3 was not detected with the promoters of other imprinted genes in 15ql l-ql3, including ZNF127, NDN, MAGEL2, IPW, which are paternally-expressed, and UBE3A and ATP IOC, which show tissue-specific maternal expression. Methyl Lys9 H3 was also not associated with the AS-IC. However,- methyl Lys4 H3 was found to be specifically associated with the promoter region of the paternal allele of the paternally-active gene NDN. Parent-specific Lys4 methylation in lymphocyte chromatin was not detected for ZNF127, MAGEL2, IPW, UBE3A, or ATPIOC.
- the PWS-IC which overlaps the SNRPN promoter, shows the most extensive pattern of modification, with cytosine methylation and H3 Lys9 methylation on the maternal allele, and histone H3 and H4 acetylation as well as histone H3 Lys4 methylation on the paternal allele.
- the paternal SNRPN promoter region is also the site of a very prominent nuclease hypersensitive site that is not present on the maternal chromosome.
- the promoter region of NDN which shows differential cytosine methylation, does not show either differential histone acetylation or differential H3 Lys9 methylation.
- the human PWS imprinting center lacks cytosine methylation in oocytes; therefore, this modification can not be the gametic imprint for the AS/PWS region.
- H3 and H4 acetylation, as well as H3 Lys4 methylation also can not be the gametic imprint because sperm lack histones, so a paternal gametic imprint can not be a histone modification.
- Methyl Lys9 H3 is a potential candidate imprinting mark that could be imposed upon histones in the PWS imprinting center during gametogenesis.
- a maternal histone modification imprint would have the unique feature of undergoing programmed erasure during spermatogenesis, when histones are removed from chromatin and replaced by protamines.
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004080288A2 (en) * | 2003-03-10 | 2004-09-23 | University Of Virginia Patent Foundation | Post-translational modifications of proteins as regulatory switches |
EP1483415A2 (en) * | 2002-02-20 | 2004-12-08 | University Of Virginia Patent Foundation | A non-invasive diagnostic test utilizing histone modification markers |
WO2005054296A1 (en) * | 2003-12-02 | 2005-06-16 | Advanced Life Science Institute, Inc. | Antibodies recognizing methyllysine, process for producing the same and utilization thereof |
EP1563093A1 (en) * | 2002-11-13 | 2005-08-17 | G6 Science Corp. | Method of identifying and assessing dna euchromatin for detecting disease |
US7074578B2 (en) | 2001-05-08 | 2006-07-11 | Chroma Therapeutics Ltd | Methods and means of histone methylation |
US7655431B2 (en) * | 2004-12-09 | 2010-02-02 | The Brigham And Women's Hospital, Inc. | Compositions and methods based upon the kinase haspin |
WO2016038145A1 (en) * | 2014-09-10 | 2016-03-17 | Fundació Institut De Ciències Fotòniques | Method for detecting cells |
US10441644B2 (en) | 2015-05-05 | 2019-10-15 | The Regents Of The University Of California | H3.3 CTL peptides and uses thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101590450B1 (en) | 2015-05-22 | 2016-02-02 | 중앙대학교 산학협력단 | Method for detecting histone modifications of the Filaggrin gene promoter and composition for diagnosing inflammatory skin diseases using thereof |
WO2017184873A2 (en) * | 2016-04-20 | 2017-10-26 | Aelan Cell Technologies, Inc. | Compositions and methods related to the methylation of histone h1.0 protein |
Family Cites Families (2)
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US5989829A (en) * | 1991-08-09 | 1999-11-23 | Washington University | Autoantibodies and their targets in the diagnosis of peripheral neuropathies |
WO2003004050A1 (en) * | 2001-07-03 | 2003-01-16 | University Of Virginia Patent Foundation | Methylation of histone h4 at arginine 3 |
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2001
- 2001-08-23 JP JP2002523932A patent/JP2004520270A/en not_active Withdrawn
- 2001-08-23 EP EP01964349A patent/EP1313756A4/en not_active Withdrawn
- 2001-08-23 WO PCT/US2001/026283 patent/WO2002018418A1/en not_active Application Discontinuation
- 2001-08-23 AU AU2001285214A patent/AU2001285214A1/en not_active Abandoned
- 2001-08-23 CA CA002420277A patent/CA2420277A1/en not_active Abandoned
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CLARK S.J. ET AL.: "Isolation of a clone containing human histone genes", NUCLEIC ACIDS RES., vol. 9, 1981, pages 1583 - 1590, XP002946170 * |
HAYASHI T. ET AL.: "Tetrahymena histone H3. Purification and two varient sequences", BIOCHEM., vol. 95, 1984, pages 1741 - 1749, XP002946171 * |
See also references of EP1313756A4 * |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7074578B2 (en) | 2001-05-08 | 2006-07-11 | Chroma Therapeutics Ltd | Methods and means of histone methylation |
EP1483415A2 (en) * | 2002-02-20 | 2004-12-08 | University Of Virginia Patent Foundation | A non-invasive diagnostic test utilizing histone modification markers |
EP1483415A4 (en) * | 2002-02-20 | 2006-02-01 | Univ Virginia | A non-invasive diagnostic test utilizing histone modification markers |
EP1563093A1 (en) * | 2002-11-13 | 2005-08-17 | G6 Science Corp. | Method of identifying and assessing dna euchromatin for detecting disease |
WO2004080288A3 (en) * | 2003-03-10 | 2004-11-18 | Univ Virginia | Post-translational modifications of proteins as regulatory switches |
WO2004080288A2 (en) * | 2003-03-10 | 2004-09-23 | University Of Virginia Patent Foundation | Post-translational modifications of proteins as regulatory switches |
WO2005054296A1 (en) * | 2003-12-02 | 2005-06-16 | Advanced Life Science Institute, Inc. | Antibodies recognizing methyllysine, process for producing the same and utilization thereof |
US7655431B2 (en) * | 2004-12-09 | 2010-02-02 | The Brigham And Women's Hospital, Inc. | Compositions and methods based upon the kinase haspin |
WO2016038145A1 (en) * | 2014-09-10 | 2016-03-17 | Fundació Institut De Ciències Fotòniques | Method for detecting cells |
US10564167B2 (en) | 2014-09-10 | 2020-02-18 | Fundació Institut De Ciències Fotóneques | Method for detecting cells |
US10441644B2 (en) | 2015-05-05 | 2019-10-15 | The Regents Of The University Of California | H3.3 CTL peptides and uses thereof |
US10849965B2 (en) | 2015-05-05 | 2020-12-01 | The Regents Of The University Of California | H3.3 CTL peptides and uses thereof |
US11185577B2 (en) | 2015-05-05 | 2021-11-30 | The Regents Of The University Of California | H3.3 CTL peptides and uses thereof |
US11925679B2 (en) | 2015-05-05 | 2024-03-12 | The Regents Of The University Of California | H3.3 CTL peptides and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
AU2001285214A1 (en) | 2002-03-13 |
EP1313756A4 (en) | 2004-12-22 |
EP1313756A1 (en) | 2003-05-28 |
CA2420277A1 (en) | 2002-03-07 |
JP2004520270A (en) | 2004-07-08 |
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