CA2432278A1 - Methods and compositions relating to cardiac-specific nuclear regulatory factors - Google Patents

Abstract

The present invention relates to a novel cardiac-specific transcription factor, myocardin. This molecule modulates the development and differentiation of cardiomyocytes and is a potent inhibitor of cell growth. Methods to exploit these observations are provided and include respecifiying non-cardiac cells into cardiac cells, stimulating cardiac tissue regeneration, and methods for treating cardiomyopathies, myocardial infarction.

Description

DESCRIPTION
METHODS AND COMPOSITIONS RELATING TO A CARDIAC-SPECIFIC
NUCLEAR REGULATORY FACTOR
BACKGROUND OF THE INVENTION
The government owns rights in the application pursuant to NIH Grant Nos.
P01 HL49953 and HL63926.
1. Field of the Invention The present invention relates generally to the fields of developmental biology and molecular biology. More particularly, it concerns proteins involved in the regulation of cardiomyocyte cell growth and development.

2'. Description of Related Art The leading cause of morbidity and mortality in industrialized countries is heart disease, particularly heart disease that is associated with myocardial infarction.
Myocardial infarction results in the loss of cardiomyocytes. Cardiomyocytes are post-mitotic cells and generally do not regenerate after birth. Furthermore, it has been discovered that they respond to mitotic signals by cell hypertrophy (Kodama et al., 1997; Pan et al., 1997) rather than by cell hyperplasia. The loss of cardiomyocytes leads to regional contractile dysfunction. In addition, the necrotized cardiomyocytes in the infarcted regions in the ventricular tissues are progressively replaced by fibroblasts to form scar tissue.
Recently, fetal cardiomyocytes transplanted in heart scar tissue limited scar expansion and prevented postinfarction heart failure (Leor et al., 1996).
Although the transplantation of fetal cardiomyocytes is a proposed treatment of heart failure, it remains impractical in the clinical setting, in part because of the difficulty of obtaining fetal heart donor tissue. Thus, it is desirable to develop a cardiomyogenic cell line that could be used to facilitate the understanding of cardiomyocyte development and to facilitate the treatment of heart diseases, such as those associated with loss of cardiomyocytes.

Although it is known that the loss of post-mitotic cardiomyocytes results in increased morbidity and mortality, very little is known about the genes that are involved in heart development. It is known that transcription factors such as d-HAND, e-HAND (Srivastava et al., 1995), MEF-2C (Edmondson et al. 1994; Lin et al. 1997), Nkx2.5/Csx, GATA4, and TEF-1 play important roles in cardiac development (Harvey, 1996), but the lack of a model for cardiomyocyte differentiation has hindered the understanding of the interactions of these genes.
A recent report revealed that murine marrow stromal cells that are treated with 5-azacyidine, a cytosine analog capable of altering expression of certain genes that may regulate differentiation, results in a cell line that differentiates into cardiomyocytes in vitro (Makino et al., 1999). This cardiomyogenic cell line demonstrated several phenotypic characteristics that are specific to cardiomyocytes, e.g., adjoining cells via intercalated discs, forming myotubes, and beating spontaneously. In addition, the expression of cardiomyocyte specific genes, such as horneobox gene N1~2.5, alpha-myosin heavy chain and atrial natriuretic factor, also are considered characteristic.
Although the proposed transplantation of fetal cardiomyocytes and cardiomyogenic cell lines are possible treatments, it is preferable to discover a treatment that eliminates any donor/species problems. Thus, identifying new regulators of cardiomyocyte growth and differentiation is an important goal in the search for therapeutics to treat myocardial tissue damage.
SUMMARY OF THE INVENTION
The present invention provides polypeptides capable of modulating cell phenotype, particularly phenotypic characteristics of cardiomyocyte cells, and polynucleotides encoding such polypeptides. In particular, pxovided herein is a family of peptides, known as myocardins, that share certain sequence homology and functional activities, as described herein. In one aspect, the polypeptides of the present invention comprise mycardin peptides and biologically active fragments thereof. In another aspect, the present invention provides isolated polynucleotides encoding a myocardin peptide including fragments thereof. Exemplary biologically active fragments of myocardin polypeptides are also provided herein.
In a further aspect, there are provided expression cassettes comprising polynucleotides encoding the polypeptides of the present invention.
Preferably, such expression cassettes further comprise one or more regulatory sequences operably linked to said polynucleotide, capable of enhancing or otherwise modulating transcription and/or translation of said polynucleotide in a target cell, for example a mammalian cell. By way of illustration, in one embodiment, an expression cassette comprising a polynucleotide encoding a myocardin polypeptide operably linked to a promoter is provided. The promoter may be an inducible promoter or a constitutive promoter. The promoter may be heterologous to the myocardin coding sequence. , Further, the promoter may be a ubiquitous promoter, for example a cytomeglovirus (CMV) promoter, rous sarcoma virus (RSV) promoter or human elongation factor (e.g., hEF-la) promoter, or it may be active only in certain tissues/cells for example a .
fibroblast specific promoter (e.g., an alpha collagen promoters) or a muscle-specific promoter (e.g., a myosin light chain-2 promoter or a a-myosin heavy chain).
The regulatory sequence of the expression cassette may further comprise a polyadenylation signal. The expression cassette may be a viral expression construct, for ,example, a retroviral vector, an adenoviral vector, an adeno-associated viral vector, a vaccina viral vector, a herpesviral vector, a polyoma viral construct, lentiviral vector or a Sindbis viral vector. The expression cassette may further comprise a second polynucleotide encoding a second polypeptide. The second..
polypeptide may be, for example, a cardiac transcription factor.
In another aspect of the present invention, there is provided an isolated nucleic acid segment comprising at least 1 S contiguous nucleotides of SEQ ID NO: 1, SEQ ID
NO: 2S, SEQ TD NO: 27 or SEQ ID NO: 29. Also provided is an isolated nucleic acid segment of SEQ ID NO: 1, SEQ ID NO: 2S, SEQ ID NO: 27 or SEQ ID NO: 29 comprising 1 S-2000 nucleotides in length. In a related aspect, there is provided a peptide of 8-SO residues comprising at least 8-12 consecutive residues of SEQ
ID NO:
2, SEQ ID NO: 26, SEQ ID NO: 28 or SEQ ID NO: 30. In another related aspect, there are provided antibodies, which may be produced by a hybridoma cell, that bind immunologically to a polypeptide comprising SEQ ID NO: 2, SEQ ID NO: 26, SEQ

ID NO: 28 or SEQ ID NO: 30, or an antigenic fragment thereof. The antibodies may be monoclonal or polyclonal antisera.
In a further aspect of the present invention, as described further below, myocardin peptides from different species are provided. By way of illustration, murine mycardin 1 (e.g., SEQ ID NOS: 2 and 30), human myocardin 1 (e.g.,. SEQ
ID
NOS: 26 and 28), human myocardin 2 (SEQ ID NO: 4) and human myocardin 3 (SEQ
117 NO: 6) are described. These myocardin peptides share localized regions of high amino acid sequence homology, particularly in the carboxyl-terminal transcription activation domain, and, particularly with respect to myocardin l and 2, in glutamine (Q) rich domains.
In still a further aspect of the invention, there is provided a transformed host cell comprising a polynucleotide encoding a myocardin polypeptide and a promoter heterologous to the myocardin-encoding polynucleotide which promoter directs the expression of the myocardin polypeptide. The host cell may be prokaryotic or eukaryotic. In a related aspect of the invention, there is provided a method of using the transformed host cell and culturing it under conditions suitable for the expression of the myocardin polypeptide. W yet another aspect, there is provided a fusion protein comprising a myocardin protein or peptide fused to a second protein or peptide.
As discussed above, heart disease, especially that resulting in a heart attack, typically results in significant cardiac dysfunction. This dysfunction can be the result of the activities of cells, especially non-cardiomyocyte cells, in the region of disease of the heart. In a further aspect of the present invention, compositions and methods are provided that alleviate the deleterious activities of such non-cardiomyocyte target cells on the functioning of the heart by modulating the phenotype of said target cells.
In preferred embodiments, the compositions and methods not only alleviate the deleterious activities of the target cell population but stimulate the target cells to engage in one or more functions typical of cardiomyocytes thereby improving myocardial functioning in the diseased region. By way of illustration, fibroblast cells typically are recruited to form scar tissue in areas of myocardium where cardiomyocyte necrosis has occurred (for example, as the result of myocardial infarction) thereby resulting in permanent, regional cardiac dysfunction.
Introduction of a composition in accordance herewith into such fibroblasts can prevent those cells from engaging in such deleterious activity and, in preferred embodiments, can actually stimulate the fibroblasts to engage in one or more functions phenotypical of cardiomyocytes (for example, spontaneous beating, formation of microtubules or adjoining to neighboring cells via intercalated discs, and expression of cardiomyocyte specific genes, such as homeobox gene Nkx2.5, alpha-myosin heavy chain and atrial natriuretic factor) thereby assisting heart function. Advantageously, introduction of such compositions in accordance herewith may additionally improve the functioning of existing cardiomyocytes by, for example, inducing hypertrophy therein.
Thus, the present compositions may serve the dual roles of stimulating fibroblast cells to engage in functions) phenotypic of cardiomyocytes and stimulating hypertrophy in existing cardiomyocytes.
In yet a further and related aspect of the present invention, there is provided a method of converting a non-cardiomyocyte target cell, such as a cardiac fibroblast into a cardiac myocyte-like cell comprising introducing into the target cell an expression cassette. The expression cassette comprises a polynucleotide encoding a myocardin polypeptide as well as one or more regulatory sequences, for example, a promoter with or without enhancer sequences, which regulatory sequences are active in the target cell and direct the expression of the polypeptide. The method may further comprise measuring cardiac and muscle cell lineage markers. In another aspect, the expression cassette may further comprise one or more additional polynucleotides encoding one or more polypeptides. By way of illustration, a second polypeptide may be a cardiac transcription factor, for example, GATA4. In a related aspect, expression of the additional polynucleotides may be under the control of the same regulatory sequences as the first polynucleotide or may be separately controlled by additional regulatory sequences.
In another aspect of the present invention, the method further comprises introducing one or more additional expression cassettes into target cells separately from introduction of the myocardin expression cassette. By way of illustration, a second expression cassette comprising a polynucleotide encoding a second polypeptide and including a second promoter able to direct expression of the second polypeptide in the target cells may be delivered to the target cell using a separate gene delivering means from that used to introduce the myocardin expression cassette.
Thus, for example, a first gene delivery vector comprising a myocardin expression cassette may be delivered simultaneously or contemporaneously with a second gene delivery vector comprising a second expression cassette. If desired, polypeptide expression may be measured, for example, by measuring transcription by RNA
hybridization, RT-PCR or Western analysis.
In yet another aspect, there is provided a method of generating a cardiomyocyte comprising introducing into a cardiac fibroblast an expression cassette.
The expression cassette comprising, for example, a polynucleotide encoding a myocardin polypeptide operatively Linked to a promoter capable of directing expression of the polypeptide. The promoter may be heterologous to the coding sequence and may be a ubiquitous (e.g., CMV) or a specific promoter (e.g., an alpha collagen promoter). The expression cassette may be introduced into the fibroblast.by any of a variety of means known to those of skill in the art. By way of illustration, Lipid-based vectors (e.g., liposomes), viral vectors (e.g., retroviral vectors, vaccine viral vectors, herpesviral vectors, polyoma viral constructs, lentiviral vectors or Sindbis viral vectors), or other macromolecular complexes capable of mediating delivery of the polynucleotide to the fibroblast or other target cell, may be employed.
In a further aspect the gene delivery vector may be modified, for example by means lcnown to those of skill in the art, to target one or more specific cell types. The expression cassette may also comprise a selectable marker, e.g., an immunologic marker. The expression cassette may further comprise a second polynucleotide encoding a second polypeptide, such as the GATA4 cardiac transcription factor.
Such a second polynucleotide may be under control of a second promoter or the same promoter as the first polynucleotide. Alternatively, an internal ribosomal entry site (IRES) may be employed between the two transgenes to permit expression of the second transgene.
In a further aspect of the present invention, there is provided a method of stimulating cardiac tissue regeneration comprising inhibiting the function of myocardin in a post-mitotic cardiomyocyte. Inhibiting may comprise providing antisense nucleic acid that inhibits transcription or translation of a myocardin mRNA.

The antisense nucleic acid may be provided by introducing an expression cassette encoding myocardin antisense RNA.
In still another aspect, there is provided a non-human transgenic animal, e.g., a mouse, comprising an expression cassette. The expression cassette comprises a .
polynucleotide encoding a myocardin peptide or protein and a promoter operably linked thereto which promoter may be heterologous to the myocardin peptide or protein encoding region. The promoter may be a constitutive or an inducible promoter. The expression cassette may further comprise selectable marker(s).
In a related aspect of the present invention, the non-human transgenic animal may comprise a defective germ-line myocardin allele or two defective germ-line myocardin alleles.
In a further aspect of the invention, there is provided a method of treating a heart disease, such as cardiomyopathy (for example, myocardial infarction or hypertension). The method comprises administering to an animal suffering from a heart disease an expression cassette, which may comprise a polynucleotide encoding a myocardin peptide or protein and a promoter operable in eukaryotic cells. The promoter may be a tissue-specific promoter. The expression cassette may be comprised within a viral expression vector, for example, a retroviral vector, an adenoviral vector, an adeno-associated viral vector, a vaccina viral vector, ' a herpesviral vector, a polyoma viral construct, a lentiviral vector or a Sindbis viral vector or witlun a non-viral vector, for example a lipid-based vector. In a related aspect, the method may comprise providing to an animal suffering therefrom a rnyocardin antisense nucleic acid.
In another related aspect, there is provided a method of alleviating one or more symptoms of a heart disease comprising inhibiting the function of myocardin in post-mitotic cardiomyocytes in the subject. Another method of alleviating one or more symptoms of a heart disease, for example in a subject with heart failure, comprises increasing the level of myocardin in fibroblasts to generate cardiomyocytes in the subj ect.
An additional aspect of the present invention is to provide compositions and methods for the identification of downstream target genes of myocardin polypeptides.

A gene delivery vector, for example an adenoviral vector, can be employed to deliver a myocardin gene to isolated cardiomyocytes thereby permitting over-expression of the myocardin polypeptide. Differences in gene profiling between control (i.e., non-transfected) cardiomyocytes and ~ transfected (i.e., myocardin-overexpressing) cardiomyocytes can then be assessed by standard methods, such as differential display and microarray (e.g., gene chip) technology. Genes that are activated by myocardin in cardiomyocytes can subsequently be evaluated as potential therapeutics, for example, using bioinformatics techniques. In yet another aspect of the present invention, there is provided a method of screening for a candidate ~ substance for an effect on myocardin regulation of cardiomyocyte development comprising: (a) providing myocardin and GATA to a cell; (b) admixing myocardin and GATA in the presence of the candidate substance; and (c) measuring the effect of the candidate substance on the expression of a cardiac lineage maxker, wherein a difference in the expression of the cardiac lineage marker, as compared to an untreated cell, indicates that the candidate substance effects myocardin regulation of cardiomyocyte development.
Exemplary cells include fibroblast and cardiomyocytes, which may be located in an animal. The modulator may incxease or decrease the expression of the cardiac lineage marker. The cardiac lineage marker may be Nkx2.5. The measuring of the expression of the cardiac lineage marker may comprise RNA hybridization, RT-PCR, immunologic detection, ELISA or immunohisotchemistry, for example.
In still yet another aspect of the invention, there is provided a method of screening for a modulator of myocardin expression comprising: (a) providing a cell that expresses a myocardin polypeptide; (b) contacting the myocardin polypeptide with a candidate substance; and (c) measuring the expression of myocardin, wherein a difference in myocardin expression, indicates that the candidate substance is a modulator of myocardin expression. The modulator may be a pharmaceutical composition. The modulator may enhance or inhibit myocardin expression.
In another aspect of the invention, there is provided a method of screening a candidate substance for myocardin binding activity comprising: (a) providing a myocardin polypeptide; (b) contacting the myocardin polypeptide with the candidate substance; and (c) determining the binding of the candidate substance to the myocardin polypeptide. The assay may be performed in a cell free system, a cell or in vivo. The candidate substance may be an inhibitor or an enhancer of myocardin.
BRIEF DESCRIPTION OF THE DRAWINGS
The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.
FIG. 1 Schematic diagram of the events of cardiac development. Cardiac precursors from the cardiac crescent (left) migrate to the midline of the embryo to form the linear heart tube, which undergoes rightward looping and eventual formation of the mature four-chambered heart. Different populations of cardiac precursor cells fated to form the aortic sac (AS), conotruncus (CT), right ventricle (RV), left ventricle (LV), and atria (A) are shown. . A schematic diagram of the structure of the mouse myocardin 1 gene is also shown. Based on human genomic sequence in public databases, we have determined that the human gene maps to chromosome 17 and encompasses 170 kb.
FIG. 2 Amino acid and nucleotide sequence of N-tenninally truncated myocardin 1. A nucleotide sequence encoding an N-terminally truncated myocardin 1 and the corresponding amino acid sequence are shown.
FIG. 3A-C Expression pattern of myocardin 1 during early heart development. FIG. 3A: Expression of myocardin lwas determined by whole-mount to mouse embryos at E7.75. Myocardin 1 transcripts can be seen localized to the cardiac crescent. FIG. 3B: Expression of myocardin 1 was determined by section to mouse embryos at E8Ø Transcripts are present throughout the heart tube in a transverse section. FIG. 3C: Expression of myocardin 1 was determined by in situ hybridizations to mouse embryos at E12.5. Transcripts are seen throughout the developing heart in a sagittal section.
FIG. 4 Expression pattern of myocardin 1 in adult mouse tissues. The expression of myocardin 1 transcripts in adult mouse tissues was analyzed by Northern blot. Transcripts are detected only in the heart. Size markers are shown to the left.
FIG. 5 Nuclear localization of myocardin 1 protein. Cos cells were transiently transfected with an expression vector encoding myocardin 1 with a Flag-epitope tag. The subcellular location of myocardin 1 protein was determined by immunostainng with anti-Flag antibody. The myocardin 1 protein is substantially localized to the nucleus. The inset in the lower right corner shows an enlargement of a single cell, with strong myocardin 1 staining in the nucleus, but excluded from the nucleoli.
FIG. 6 Structure of myocardin 1 and mapping of transcription activation domains. A schematic diagram of myocardin 1 is shown at the top. The nuclear localization sequence (NLS) is located between residues f17 and 126, within a basic region. A glutamine-rich (Q) domain is located between residues 159-192. The transcription activation domain is located at the carboxyl-terminus. Portions of myocardin 1 were fused to the DNA binding domain of yeast GAL4 and tested in transfected Cos cells for transcriptional activity against a GAL4-dependent luciferase reporter. Relative transcriptional activities of different myocardin 1 fragments are shown at the bottom. The carboxyl-terminus is an extremely potent transcription activation domain, able to activate, the reporter over 1000-fold, to a level comparable to that of the powerful viral coactivator VP16 (not shown).
FIG. 7A-D Trans-activation of the SM22 promoter by myocardin 1. Cos cells were transiently transfected with a luciferase reporter gene containing the 1.4 kb SM22 promoter and expression vectors encoding myocardin 1 and SRF, as indicated.
Forty eight hr later, cells were harvested and luciferase activity was assayed. FIG. 7A:
shows activity of the wild-type SM22 promoter, which is transactivated about fold by myocardin 1. FIG. 7B: shows activity of the SM22 promoter with a mutation in the distal CArG box (CArG-far). This promoter is also activated by myocardin 1, but not to the same extent as the wild-type promoter. FIG. 7C: shows activity of the SM22 promoter with a mutation in the proximal CArG box (CArG-near). This promoter has lost almost all responsiveness to myocardin 1, as has the promoter with both CArG boxes mutated (FIG. 7D).

FIG. 8 Myocardin 1 and MEF2C cooperatively activate the MLC2V
promoter. Cos cells were transiently transfected with a luciferase reporter gene containing the MLC2V promoter and expression vectors encoding myocardin 1 and MEF2C, as indicated. Forty eight hours later, cells were harvested and luciferase activity was assayed. The results show that myocardin 1 and MEF2C
synergistically activate MLC2V transcription.
FIG. 9 GATA4 represses myocardin 1 activation of the ANF promoter.
HeLa cells and Cos cells were transiently transfected with a luciferase reporter gene containing the ANF promoter and expression vectors encoding myocardin 1 and GATA4 (1 = I00 ng anf luc; 2 = 100 ng anf luc, 100 ng myocardin; 3 = 100 ng anf luc, 10 ng GATA4; 4 = 100 ng anf luc, 20 ng GATA4; 5 = 100 ng anf luc, 50 ng GATA4; 6 = 100 ng anf luc, I00 ng GATA4; 7 = 100 ng anf luc, 100 ng myocardin, ng GATA4; 8 =100 ng anf luc, 100 ng myocardin, 20-ng GATA4; 9 = 100 ng anf luc, 100 ng myocardin, 50 ng GATA4; 10 =100 ng anf luc, 100 ng myocardin, 100 ng GATA4). Forty eight hours later, cells were harvested and luciferase activity was assayed. The results show that activation of ANF transcription by myocardin 1 is repressed in the presence of GATA4.
FIG. 10 Myocardin 1 and Nkx2.5 cooperatively activate the a-MHC
promoter. HeLa cells were transiently transfected with a luciferase reporter gene containing the a-MHC promoter and expression vectors encoding myocardin 1 and Nkx2.5, as indicated. Forty eight hr later, cells were harvested and luciferase activity was assayed. The results show that myocardin 1 and Nkx2.5 synergistically activate a-MHC transcription.
FIG. 11 Overexpression of myocardin induces serial assembly of sarcomeres in cardiomyoc~tes. Cardiornyocytes were infected with adenoviruses expressing either myocardin(Ad-myocardin) or 13-galactosidase(Ad-LacZ), serum deprived, and immunostained with anti-sarcomeric-a-actininat antibody 24 hour post-infection.
FIG. 12 Overexpression of myocardin induces ANF expression in cardiomyocytes. Cardiomyocytes were infected with adenoviruses expressing either myocardin (Ad-myocardin) or l3-galactosidase (Ad-LacZ), serum deprived, and immunostained with anti-ANF antibody 24 hour post-infection. Images were captured at two different magnifications (x20, x100).
FIG. 13 GATA4 and mvocardin 1 activate of the NKX2.5 promoter. HeLa cells and Cos cells were transiently transfected with a luciferase reporter gene containing the NKX2.5 promoter and expression vectors encoding myocardin I and GATA4 (1 = 100 ng nl~-luc; 2 = 100 ng nkxf luc, 500 ng myocardin; 3 = 100 ng nkx-luc, 10 ng GATA4; 4 = 100 ng nkx-luc, 20 ng GATA4; 5 = 100 ng nkx-luc, 50 ng GATA4; 6 = 100 ng nkx-luc, 100 ng GATA4; 7 = 100 ng nkx-luc, 500 ng myocardin, ng GATA4; 8 = 100 ng nkx-luc, 500 ng myocardin, 20 ng GATA4; 9 = 100 ng nkx-luc, 500 ng myocardin, 50 ng GATA4; 10 = 100 ng nkx-luc, 500 ng myocardin, 100 ng GATA4). Forty eight hours later, cells were harvested and luciferase activity was assayed. The results show activation of NKX2.5 transcription by myocardin and GATA4.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
Heart disease is the number one cause of death and hospitalization in the industrialized world, due in large part to the irreversible nature of the damage sustained by the heart following heart attack and other acquired and congenital diseases. At present, the only means of repairing a damaged heart is through complicated surgery and/or heart transplant, which have obvious financial and medical shortcomings for the patient. The possibility of regenerating cardiac muscle cells within the intact human heart following damage represents one of the most important challenges in cardiovascular medicine. Perhaps the greatest chance for success in this area is to identify "master" control genes for cardiac development and to use these genes to reprogram non-muscle cells to a cardiac muscle cell fate.
A major barrier to cardiac regeneration is the inability of postnatal cardiomyocytes to divide. In principle, cardiac repair could be achieved through a release from this block to cell cycle progression. However, such an approach, which might involve introduction of oncogenes or other powerful stimulators of cell proliferation into the heart, has an obvious downside unless such regulators were somehow cardiac-specific and could be prevented from inducing uncontrolled proliferation of other cell types. Because about 40% of the cells in the myocardium are fibroblasts, an alternate approach would be to reprogram these cells to a cardiomyocyte fate at sites of cardiac damage through targeted delivery of cardiac master control genes.
The loss of cardiomyocytes leads to reduced contractile function of the heart resulting in increased morbidity and mortality. The present inventors now report the discovery of novel cardiac-specific factors, referred to herein as myocardins.
One such myocardin, myocardin 1, is expressed in cardiac and smooth muscle.
Moreover, myocardin 1 is first expressed as early as the linear heart tube stage, embryonic day 8 (E8) in the mouse. This expression is restricted to the heart and to a subset of vascular smooth muscle cells throughout embryogenesis to adulthood. The subcellular distribution of myocardin 1 is localized in the nucleus. Moreover, expression of myocardin 1 in transfected cells appears to result in growth arrest of the cells.
To determine the functions of myocardin 1, the inventors transfected myocardin 1 expression plasmids into fibroblasts (Cos and HeLa cells) along with expression plasmids for the cardiac transcription factor GATA4. The cells were transiently transfected using FuGENE 6 (Boehringer-Mannheim), according to manufacturer's instructions. Briefly, 0.1 ~g of expression plasmid encoding myocardin 1 or the other indicated cardiac transcription factors, along with the indicated luciferase plasmids, were mixed with 3 q1 of FuGENE 6 and added to cells in six-well plates. Cells were harvested 48 hr later and luciferase activity was determined in cell extracts. In all transfections, the amount of DNA per well was kept constant by adding the corresponding vector. CMV-lacZ, which contains the lacZ
gene under control of the constitutive cytomegalovirus promoter, was included in all transfections as an internal control to normalize for variations in transfection efficiency. The results demonstrated that myocardin 1, plus GATA4, transactivates regulatory sequences for the cardiac specif c homeobox Nkx2.5, which is the earliest marker for the cardiac lineage in vertebrates. These results indicate that myocardin 1 plays an important role in regulating cardiomyocyte development.

Based upon the functional activity of the marine myocardin 1 and having its complete cDNA sequence, the inventors have been able to identify other myocardins, which they have characterized. Initial searches of DNA sequence databases with myocardin 1 sequence revealed a number of related sequences. Most of these sequences are short sequences (for example, ESTs) that share homology to only small regions of myocardin 1. None of the sequences located have been identified as encoding proteins having any particular function, much less any faction related to cell regulation, particularly cardiac cell regulation. However, using these techniques in combination with the information obtained previously regarding the marine myocardin, the inventors have identified two sequences that share significant homology with myocaxdin 1. These appear to be partial sequences from two additional myocardin genes. cDNA clones for these two related genes, now designated myocardin 2 and myocardin 3, have been obtained. A comparison of the three myocardin species identified has revealed localized regions of high amino acid homology between the proteins, particularly in the carboxyl-terminal transcription activation domain. By Northern analysis, it was shown that that myocardin 2 is ubiquitous, and that myocardin 3 appears restricted to heart and liver. These factors may be dimerization partners for myocardin 1, and/or may serve analogous functions to myocardin 1 in the heart and/or other tissues.
Using similar techniques and information about the marine myocardin 1, the inventors have also been able locate the genomic sequence of the human homolog for myocardin 1 within a particular segment of chromosome 17 (Accession No.
AC005358) and to determine the location of its exons and introns, enabling identification of the human cDNA sequence. The best EST match fox myocardin 1 is Accession No. AI607474, for myocardin 2 is Accession No. BE311634, and for myocardin 3 is Accession No. AW500597.
The discovery of proteins that function to regulate cardiomyocyte growth and differentiation is important, both for advancing the basic understanding of heart development and to provide novel targets for the development of drugs and/or biotechnological methods to treat cardiac disease, for example by stimulating the growth and differentiation of cells into cardiomyocytes after a patient has suffered tissue damage as a result of cardiomyopathy. Since myocardin appears to act as an early cardiac inducing factor with the capacity to induce cardiomyocyte development;
and has the potential to reprogram cardiac fibroblasts, which constitute 40%
of the cell types in. the heart, to a cardiomyocyte type fate, it may be used in a variety of ways to directly treat cardiac disease and to develop additional treatments for cardiac disease. Further, because myocardin also appears to induce hypertrophy in cardiomyocytes, its overexpression may provide an additional benefit in the treatment of heart disease by, for example, improving the functioning of dysfunctional or malfactional cardiomyocytes.
I. Nucleic Acids In one aspect, the present invention provides nucleic acid sequences encoding cardiac cell regulatory factors designated myocardins. In a further aspect the coding sequence (as well as substantial non-coding protions) of a novel, N-terminally tnmcated cardiac-specific factor, designated herein as myocardin 1, is provided (SEQ
ID NOS 1 and 25). In yet another aspect of the present invention, provided herein are nucleic acids encoding mouse and human myocardin l, SEQ ID NOS: 29 and 27;
respectively. The present invention is not limited in scope to any specific nucleic acid sequences disclosed herein as one of ordinary skill in the art could, using these nucleic acid sequences, readily identify related homologs, including, for example, homologs present in any of various species (e.g., rat, rabbit, dog, monkey, gibbon, chimp, ape, baboon, cow, pig, horse, sheep, cat and other species).
As discussed below, a "myocardin nucleic acid sequence" may contain a variety of different bases and yet still produce a myocardin polypeptide according to the present invention. Such polypeptides will generally be functionally equivalent to, and/or structurally indistinguishable, from the human, mouse and other genes disclosed herein. Additionally, nucleic acid sequences encoding fragments of myocardin are provided herein. For example, fragments having increased activity (e.g., the carboxy terminal fragments described in FIG. 6) as compared with the full-length myoeardin polypeptide are described. Similarly, it will be readily recognized that fragments may be employed as probes, for example in the isolation of homologous sequences. Thus, as will be apparent to those of skill in the art, fragments of the myocardin-encoding nucleic acid sequences as well as homologs thereof are likewise contemplated herein.
Similarly, any reference to a nucleic acid should be read as encompassing vectors and host cells containing that nucleic acid and, in some cases, capable of expressing the product of that nucleic acid. In addition to therapeutic considerations, cells expressing nucleic acids of the present invention may prove useful in the context of screening for agents that induce, repress, inhibit, augment, interfere with, block, abrogate, stimulate or enhance the function ofmyocardin.
A. Nucleic Acids Encoding Myocardin Nucleic acids according to the present invention may encode an entire myocardin gene, a domain of myocardin, or any other fragment of myocardin as set forth herein. The nucleic acid may be derived from genomic DNA, i.e., cloned directly from the genome of a particular organism. In preferred embodiments, however, the nucleic acid comprises complementary DNA (cDNA). Also contemplated is a cDNA plus a natural intron or an intron derived from another gene;
such engineered molecules are sometime referred to as "mini-genes." At a minimum, these and other nucleic acids of the present invention may be used as molecular weight standards in, for example, gel electrophoresis.
The term "cDNA" is intended to refer to DNA prepared using messenger RNA
(mRNA) as template. The advantage' of using a cDNA, as opposed to genomic DNA
or DNA polymerized from a genomic, non- or partially-processed RNA template, is that the cDNA primarily contains coding sequences of the corresponding protein.
There may be times when the full or partial genomic sequence is preferred, such as where the non-coding regions are required for optimal expression or where non-coding regions such as introns are to be targeted in an antisense strategy.
It also is contemplated that a given myocardin polynucleotide may be represented by natural or synthetic variants that have slightly different nucleic acid sequences but, nonetheless, encode the same or homologous protein (see Table 1 below).

As used in this application, the term "a polynucleotide encoding a polypeptide"
refers to a nucleic acid molecule that is isolated free of total cellular nucleic acid, including for example, a synthetic polynucleotide. In exemplary embodiments, the invention concerns a nucleic acid sequence essentially as set forth in SEQ ID
NO: 1, SEQ 1D NO: 25, SEQ ID NO: 27 or SEQ ID NO: 29. The term "comprises SEQ TD
NO: 1 or 27" means that the nucleic acid sequence substantially corresponds to a portion of the aforementioned SEQ ID NO: 1 or 27 and likewise for other SEQ ID
NOS providing nucleic acid sequences. The term "functionally equivalent codon"
is used herein to refer to codons that encode the same amino acid, such as the six codons for arginine or serine (Table I, below), and also refers to codons that encode biologically equivalent amino acids, as discussed in the following pages.

Amino Acids Codons Alariine Ala A GCA GCC GCG GCU

Cysteine Cys C UGC UGU
.

Aspartic Asp D GAC GAU
acid Glutamic Glu E GAA GAG
acid PhenylalaninePhe F UUC UUU

Glycine Gly G GGA GGC GGG GGU

Histidine His H CAC CAU

Isoleucine Ile I AUA AUC AUU

Lysine Lys K AAA AAG

Leucine Leu L UUA UUG CUA CUC CUG CUU

Methionine Met M AUG

Asparagine Asn N AAC AAU

Proline Pro P CCA CCC CCG CCU

Glutamine Gln Q CAA CAG

Arginine Arg R AGA AGG CGA CGC CGG CGU

Serine Ser S AGC UCA UCC UCG UCU
AGU

Threonine Thr T ACA ACC ACG ACU

Valine Val V GUA GUC GUG GUU

Tryptophan Trp W UGG

Tyrosine Tyr Y UAC UAU

Allowing for the degeneracy of the genetic code, sequences that have at least about 50%, usually at least about 60%, more usually about 70%, most usually about 80%, preferably at least about 90% and most preferably about 95% of nucleotides that are identical to the nucleotides of a sequence set forth herein, for example SEQ ID

NO: 1 or 27 are contemplated. Sequences that are essentially the same as those set forth in SEQ ID NO: 1 or 27 also may be functionally defined as sequences that are capable of hybridizing to a nucleic acid segment containing the complement of SEQ
ID NO: 1 or 27 under standard conditions and likewise for other nucleotide sequences set forth herein.
The DNA segments of the present invention include those encoding biologically functional equivalent myocardin proteins, peptides and fragments thereof, as described elsewhere herein. Such sequences may arise as a consequence of codon redundancy and/or amino acid functional equivalency that are known to those of skill in the art. For example, polynucleotides encoding myocardin peptides analogous to the exemplary myocardin protein of SEQ m NO: 2 or 28 are likewise contemplated herein. As discussed fiu-ther below, and as lmown to those of skill in the art, various amino acid substitutions, deletions and/or additions may be made to a known amino acid sequence without adversely affecting the fimction andlor usefulness thereof.
Alternatively, functionally equivalent proteins or peptides may be created via the application of recombinant DNA technology, in which changes in the protein structure may be engineered, based on considerations of the properties of the amino acids being exchanged. Changes designed by man may be introduced through the application of site-directed mutagenesis techniques or may be introduced randomly and screened later for the desired function, as described below.
B. Oligonucleotide Probes and Primers Naturally, the present invention also encompasses DNA segments that are complementary, or essentially complementary, to the sequences set forth herein, for example in SEQ m NO:1. Nucleic acid sequences that are "complementary" are those that are capable of base-pairing according to-the standard Watson-Crick complementary rules. As used herein, the terms "complementary sequences" and "essentially complementary sequences" means nucleic acid sequences that are substantially complementary to, as rnay be assessed by the same nucleotide comparison set forth above, or are able to hybridize to a nucleic acid segment of one or more suequences set forth herein, for example SEQ m NO:1 or 27, under relatively stringent conditions such as those described herein. Such sequences may encode an entire myocardin protein or peptide or functional or non-functional fragments thereof.

The hybridizing segments may be short oligonucleotides. Sequences of 17 bases long should occur only once in the human genome and, therefore, suffice to specify a unique target sequence. Although shorter oligomers are easier to make and increase in vivo accessibility, numerous other factors are involved in determining the specificity of hybridization. Both binding affinity and sequence specificity of an oligonucleotide to its complementary target increases with increasing length. It is contemplated that exemplary oligonucleotides of 8, 9, 10, 11, 12, 13, 14, 1S, 16, 17, 18, 19, 20, 2S, 30, 35, 40, 4S, 50, 5S, 60, 65, 70, 75, 80, 85, 90, 95, 100 or more base pairs will be used, although others are contemplated. Longer polynucleotides encoding 250, 500, 750, 1000, 1250, 1500, 2000, 2500, 3000 or 4000 bases and longer are contemplated as well.
Such oligonucleotides will find use, for example, as probes in Southern and Northern blots and as primers in amplification reactions.
Suitable hybridization conditions will be well known to those of skill in the art.
In certain applications, for example, substitution of amino acids by site-directed mutagenesis, it is appreciated that lower stringency conditions are required.
Under these conditions, hybridization may occur even though the sequences of probe and target strand are not perfectly complementary, but are mismatched at one or more positions.
Conditions may be rendered less stringent by increasing salt concentration and decreasing temperature. For example, a medimn stringency condition could be provided by about 0.1 to 0.25 M NaCI at temperatures of about 37°C to about 55°C, while a low stringency condition could be provided by about 0.15 M to about 0.9 M salt, at temperatures ranging from about 20°C to about SS°C. Thus, hybridization conditions can be readily manipulated, and thus will generally be a method of choice depending on the desired results.
In other embodiments, hybridization may be aclueved under conditions of, for example, 50 mM Tris-HCl (pH 8.3), 75 mm KCI, 3 mM MgCl2, 10 mM dithiothreitol, at temperatures between approximately 20°C to about 37°C. Other hybridization conditions utilized could include approximately 10 mM Tris-HCl (pH 8.3), SO mM
KCI, 1.5 p,M MgCl2, at temperatures ranging from approximately 40°C to about 72°C.
Formamide and SDS also may be used to alter the hybridization conditions.

One method of using probes and primers of the present invention is in the search for genes related to myocardin proteins and peptides, including for example, myocardin proteins from other species: Normally, the target DNA will be a genomic or cDNA
library, although screening may involve analysis of RNA molecules. By varying the stringency of hybridization, and the region of the probe, different degrees of homology may be discovered.
Another way of exploiting probes and primers of the present invention is in site-directed, or site-specific mutagenesis. Site-specific mutagenesis is a techtuque useful in the preparation of individual peptides, or biologically functional equivalent proteins or peptides, through specific mutagenesis of the underlying DNA. The technique further provides a ready ability to prepare and test sequence variants, incorporating one or more of the foregoing considerations, by introducing one or more nucleotide sequence changes into the DNA. Site-specific mutagenesis allows the production of mutants through the use of specific oligonucleotide sequences which encode the DNA sequence of the desired mutation, as well as a sufficient number of adjacent nucleotides, to provide a primer sequence of sufficient size and sequence complexity to .form a stable duplex on both sides of the deletion junction being traversed. Typically, a primer of about 17 to 25 nucleotides in length is preferred.
The technique typically employs a bacteriophage vector that exists in both a single stranded and double-stranded form. Typical vectors useful in site-directed mutagenesis include vectors such as the M13 phage. These phage vectors are commercially available and their use is generally well known to those skilled in the art. Double-stranded plasmids are also routinely employed in site-directed mutagenesis, which eliminates the step of transferring the gene of interest from a phage to a plasmid.
In general, site-directed mutagenesis is performed by f rst obtaining a single-stranded vector, or melting of two strands of a double-stranded vector which includes within its sequence a DNA sequence encoding the desired protein. An oligonucleotide primer bearing the desired mutated sequence is synthetically prepared. This primer is then annealed with the single-stranded DNA preparation, taking into account the degree of mismatch when selecting hybridization conditions, and subjected to DNA

polymerizing enzymes such as E. coli polymerase I Klenow fragment, in order to complete the synthesis of the mutation-bearing strand. Thus, a heteroduplex is formed wherein one strand encodes the original non-mutated sequence and the second strand bears the desired mutation. This heteroduplex vector is then used to transform appropriate cells, such as E. coli cells, and clones are selected that include recombinant vectors bearing the mutated sequence arrangement.
The preparation of sequence variants of the selected gene using site-directed mutagenesis is provided as a means of producing potentially useful species and is not meant to be limiting, as there are other ways in which sequence variants of genes may be obtained. For example, recombinant vectors encoding the desired gene may be treated with mutagenic agents, such as hydroxylamine, to obtain sequence variants.
C. Antisense Constructs Antisense methodology takes advantage of the fact that nucleic acids tend to pair with "complementary" sequences. By complementary, it is meant that polynucleotides are those which are capable of base-pairing according to the standard Watson-Crick complementarity rules. That is, the larger purines will base pair with the smaller pyrimidines to form combinations of guanine paired with cytosine (G:C) and adenine paired with either thymine (A:T) in the case of DNA, or adenine paired with uracil (A:T~ in the case of RNA. Inclusion of less common bases such as inosine, 5-methylcytosine, 6-methyladenine, hypoxanthine and others in hybridizing sequences does not interfere with pairing.
Targeting double-stranded (ds) DNA with polynucleotides leads to triple-helix formation; targeting RNA will lead to double-helix formation. Antisense polynucleotides, when introduced into a target cell, specifically bind to their target polynucleotide and interfere with transcription, RNA processing, transport, translation and/or stability. Antisense RNA constructs, or DNA encoding such antisense RNA's, may be employed to inhibit gene transcription or translation or both within a host cell, either ifs vitro or in vivo, such as within a host animal, including a human subject.
Antisense constructs may be designed to bind to the promoter and/or other control regions, exons, introns or even exon-intron boundaries of a gene. It is contemplated that the most. effective antisense constructs will include regions complementary to intron/exon splice junctions. Thus, it is proposed that a preferred embodiment includes an antisense construct with complementarity to regions within 50-200 bases of an intron-exon splice junction. It has been observed that some exon sequences can be included in the construct without seriously affecting the target selectivity thereof. The amount of exonic material included will vary depending on the particular exon and intron sequences used. One can readily test whether too much exon DNA is included simply by testing the constructs if2 vitf°o to determine whether normal cellular function is affected or whether the expression of related genes having complementary sequences is affected.
As stated above, "complementary" or "antisense" means polynucleotide sequences that are substantially complementary over their entire length and have very few base mismatches. For example, sequences of fifteen bases in length may be termed complementary when they have complementary nucleotides at thirteen or.
fourteen positions. Naturally, sequences which are completely c~rnplementary will be sequences which are entirely complementary throughout their entire length and have no base mismatches. Other sequences with lower degrees of homology also are contemplated. For example, an antisense construct which has limited regions of lugh homology, but also contains a non-homologous region (e.g., ribozyme; see below) could be designed. These molecules, though having less than 50% homology, would bind to target sequences under appropriate conditions.
It may be advantageous to combine portions of genomic DNA with cDNA or synthetic sequences to generate specific constructs. For example, where an intron is desired in the ultimate construct, a genomic clone will need to be used. The cDNA or a synthesized polynucleotide may provide more convenient restriction sites for the remaining portion of the construct and, therefore, would be used for the rest of the sequence.
D. Ribozymes Although proteins traditionally have been used for catalysis of nucleic acids, another class of macromolecules has emerged as useful in this endeavor.
Ribozymes are RNA-protein complexes that cleave nucleic acids in a site-specific fashion.

Ribozymes have specific catalytic domains that possess endonuclease activity (Kim and Cook, 1987; Gerlach et al., 1987; Forster and Symons, 1987). For example, a large number of ribozymes accelerate phosphoester transfer reactions with a high degree of specificity, often cleaving only one of several phosphoesters in an oligonucleotide substrate (Cook et al., 1981; Michel and Westhof, 1990;
Reinhold-Hurek and Shub, 1992). This specificity has been attributed to the requirement that the substrate bind via specific base-pairing interactions to the internal guide sequence ("IGS") of the ribozyme prior to chemical reaction.
Ribozyme catalysis has primarily been observed as part of sequence-specific cleavage/ligation reactions involving nucleic acids (Joyce, 1989; Cook et al., 1981).
For example, U.S. Patent 5;354,855 reports that certain ribozymes can act as endonucleases with a sequence specificity greater than that of known ribonucleases and approaching that of the DNA restriction enzymes. Thus, sequence-specific ribozyme-mediated inhibition of gene expression may be particularly suited to therapeutic applications (Scanlon et al., 1991; Sarver et al., 1990).
Recently, it was reported that ribozymes elicited genetic changes in some cells lines to which they were applied; the altered genes included the oncogenes H-ras, c-fos and genes of HIV.
Most of this work involved the modification of a target rnRNA, based on a specific mutant codon that is cleaved by a specific ribozyme.
E. Vectors for Cloning, Gene Transfer and Expression Within certain embodiments expression vectors are employed to express a myocardin polypeptide product, which can then be purified and, for example, be used to vaccinate animals to generate antisera or monoclonal antibody with which further studies may be conducted. In other embodiments, the expression vectors are used in gene therapy. Expression requires that appropriate signals be provided in the vectors, including, for example, various regulatory elements, such as enhancers/promoters from viral and/or mammalian sources that are involved in driving expression of the genes of interest in host cells. Elements designed to optimize messenger RNA
stability and translatability in host cells also can be used. The conditions for the use of a number of dominant dmg selection markers for establishing permanent, stable cell clones expressing the products are also provided, as is an element that links expression of the drug selection markers to expression of the polypeptide.

(i) Regulatory Elements Throughout this application, the term "expression construct" or "expression cassette" is meant to include any type of genetic construct containing a nucleic acid coding for a gene product in which part or all of the nucleic acid encoding sequence is capable of being transcribed. The transcript may be translated into a protein or polypeptide, but it need not be. In certain embodiments, expression includes both-transcription of a gene and translation of mRNA into a gene product. In other embodiments, expression only includes transcription of the nucleic acid encoding a gene of interest.
As used herein, regulatory elements (or sequences) are nucleotide sequences that enhance or otherwise modulate transcription and/or translation or that stabilize transcription and/or translation products. Thus, for example, promoters operably linked to a coding sequence of an expression construct enhance transcription of that coding sequence and polyadenylation sequences operably linked to a coding sequence.
modulate polyadenylation of the gene transcript. Exemplary regulatory sequences can include, without limitation, promoters enhancers, introns, termination sequences, polyadenylation sequences, stabilization sequences and the like.
In certain embodiments, the nucleic acid encoding a gene product is operably linked and under transcriptional control of a promoter. A "promoter" refers to a DNA
sequence recognized by the synthetic machinery of the cell, or introduced synthetic machinery, required to initiate the specific transcription of a gene. The phrase "under transcriptional control" means that the promoter is in the correct location and orientation in relation to the nucleic acid to control RNA polymerase initiation and expression of the gene.
The term promoter will be used here to refer to a group of transcriptional control modules that are clustered around the initiation site for RNA
polymerase II.
Much of the thinking about how promoters are organized derives from analyses of several viral promoters, including those for the HSV thymidine kinase (tk) and early transcription units. These studies, augmented by more recent work, have shown that promoters are typically composed of discrete functional modules, each consisting of approximately 7-20 by of DNA, and containing one or more recognition sites for transcriptional activator or repressor proteins.
At least one module in each promoter functions to position the start site for RNA synthesis. The best known example of this is the TATA .box, but in some promoters lacking a TATA box, such as the promoter for the mammalian terminal deoxynucleotidyl transferase gene and the promoter for the SV40 late genes, a discrete element overlying the start site itself helps to fix the place of initiation.
Additional promoter elements regulate the frequency of transcriptional initiation. Typically, these axe located in the region 30-110 by upstream of the start site, although a number of promoters have recently been shown to contain functional elements downstream of the start site as well. The spacing between promoter elements frequently is flexible, so that promoter function is preserved when elements are inverted or moved relative to one another. In the tk promoter, the spacing between promoter elements can be increased to SO by apart before activity begins to decline.
Depending on the promoter, it appeaxs that individual elements can function either co-operatively or independently to activate transcription.
In certain embodiments, the human cytomegalovirus (CMV) immediate early gene promoter, the SV40 early promoter, the Rous sarcoma virus (RSV) long terminal repeat, a human elongation factor (hEF) promoter, rat insulin promoter or glyceraldehyde-3-phosphate dehydrogenase promoter can be used to obtain high-level expression of the coding sequence of interest. The use of other viral or mammalian cellular or bacterial phage promoters which are well known in the art to achieve expression of a coding sequence of interest is contemplated as well, provided that the levels of expression are sufficient fox a given purpose.
By employing a promoter with well-known properties, the level and pattern of expression of the protein of interest following transfection or transformation can be optimized. By way of illustration, a ubiquitous, strong (i.e., high activity) promoter may be employed to provide abundant gene expression in a group of host cells, or a tissue-specific promoter may be employed to target gene expression to one or more specific cell types. Further, selection of a promoter that is regulated in response to specific physiologic signals can permit inducible expression of the gene product.

Tables 2 and 3 list several regulatory elements that may be employed, in the context of the present invention, to regulate the expression of the gene of interest.
This list is not intended to be exhaustive of all the possible elements involved in the promotion of gene expression but, merely, to be exemplary thereof.
Enhancers are genetic elements that increase transcription from a promoter located at a distant position on the same molecule of DNA. Enhancers are organized much like promoters. That is, they are composed of many individual elements, each of which binds to one or more transcriptional proteins.
The basic distinction between enhancers and promoters is operational. An enhancer region as a whole is typically able to stimulate transcription at a distance;:.
this need not be true of a promoter region or its component elements. On the other hand, a promoter typically has one or more elements that direct initiation of RNA
synthesis at a particular site and in a particular . orientation, whereas enhancers.' generally lack these specificities. Promoters and enllancers are often overlapping and contiguous, often seeming to have a very similar modular organization.
Tables 2 and 3, provided below, list several regulatory elements that may be employed, in the context of the present invention, to regulate the expression of the .
gene of interest. This list is not intended to be exhaustive of all the possible elements involved in the promotion of gene expression but, merely, to be exemplary thereof.
Other promoter/enhancer combinations (see, e.g., the Eukaryotic Promoter Data Base EPDB) could also be used to drive expression of the gene. Eukaryotic cells can suppout cytoplasmic transcription from certain bacterial promoters if the appropriate bacterial polymerase is provided, either as part of the delivery complex or as an additional genetic expression construct.

Promoter and/or Enhancer Promoter/Enhancer References Immunoglobulin HeavyBanerji et al., 1983; Gilles et al., Chain 1983; Grosschedl et al., 1985; Atchinson et al., 1986, 1987;
Imler et al., 1987; Weinberger et al., 1984; Kiledjian et al., 1988;
Porton et al.; 1990 Immunoglobulin LightQueen et al., 1983; Picard et al., 1984 Chain T-Cell Receptor Luria et al., 1987; Winoto et al., 1989;
Redondo et al.;

HLA DQ a and/or Sullivan et al., 1987 DQ (3 (3-Interferon Goodbourn et al., 1986; Fujita et al., 1987; Goodbourn ;
et al., 1988 Interleukin-2 Greene et al., 1989 Interleukin-2 ReceptorGreene et al., 1989; Lin et al., 1990 MHC Class II 5 Koch et al., 1989 MHC Class II HLA-DRaSherman et al., 1989 (3-Actin Kawamoto et al., 1988; Ng et al.; 1989 Muscle Creatine Jaynes et al., 1988; Horlick et al., Kinase 1989; Johnson et al., (MCK) 1989 Human Elongation Uetsuki, et al., 1989; Wakabayashi-Ito, Factor-lA (hEF-lA et al., 1994 or hEF-1 a) Prealbumin Costa et al., 1988 (Transthyretin) Elastase I Ornitz et al., 1987 Metallothionein Karin et al., 1987; Culotta et al., (MTII) 1989 Collagenase Pinkert et al., 1987; Angel et al., 1987a Albumin Pinkert et al., 1987; Tronche et al., 1989, 1990 a-Fetoprotein Godbout et al., 1988; Campere et al., t-Globin Bodine et al., 1987; Perez-Stable et al., 1990 [3-Globin Trudel et al., 1987 c-fos Cohen et al., 1987 Promoter and/or Enhancer Promoter/Enhancer References c-HA-sas Triesman, 1986; Deschamps et al., 1985 Insulin Edlund et al., 1985 Neural Cell AdhesionHirsh et al., 1990 Molecule (NCAM) al-Antitrypain Latimer et al., 1990 H2B (TH2B) Histone Hwang et al., 1990 Mouse and/or Type Ripe et al., 1989 I

Collagen Glucose-Regulated Chang et al., 1989 Proteins (GRP94 and GRP78) .

Rat Growth Hormone Larsen et al., 1986 .

Human Serum AmyloidEdbrooke et al., 1989 A

(SAA) Troponin I (TN I) Yutzey et al., 1989 Platelet-Derived Pech et al., 1989 Growth Factor (PDGF) Duchenne Muscular Klamut et al., 1990 Dystrophy SV40 Banerji et al., 1981; Moreau et al., 1981; Sleigh et al., 1985; Firak et al., 1986; Herr et al., 1986; Imbra et al., 1986; Kadesch et al., 1986; Wang et al., 1986; Ondek et al., 1987; Kuhl et al., 1987; Schaffner et al., 1988 Polyoma Swartzendruber et al., 1975; Vasseur et al., 1980;

Katinka et al., 1980, 1981; Tyndell et al., 1981;

Dandolo et al., 1983; de Villiers et al., 1984; Hen et al., 1986; Satake et al., 1988; Campbell and/or Villarreal, Retroviruses Kriegler et al., 1982, 1983; Levinson et al., 1982;

Kriegler et al., 1983, 1984a, b, 1988;
Bosze et al., 1986; Miksicek et al., 1986; Celander et al., 1987;

Thiesen et al., 1988; Celander et al., 1988; Choi et al., 1988; Reisman et al., 1989 Promoter and/or Enhancer Promoter/Enhancer References Papilloma Virus Campo et al., 1983; Lusky et al., 1983;
Spandidos and/or Wilkie, 1983; Spalholz et al., 1985; Lusky et al., 1986; Cripe et al., 1987; Gloss et al., 1987; Hirochika et al., 1987; Stephens et al., 1987;
Glue et al., 1988 Hepatitis B Virus Bulla et al., 1986; Jameel et al., 1986;
Shaul et al., 1987; Spandau et al., 1988; Vannice et al., 1988 Human Muesing et al., 1987; Hauber et al., 1988; Jakobovits Immunodeficiency et al., 1988; Feng et al., 1988; Takebe Virus et al., 1988;

Rosen et al., 1988; Berkhout et al., 1989; Laspia et al., 1989; Sharp et al., 1989; Braddock et al., 1989 Cytomegalovirus Weber et al., 1984; Boshart et al., (CMV) 1985; Foecking et al., 1986 Rous sarcoma virus Gorman, et al., 1982; Guzman, et al., (RSV) Gibbon Ape LeukemiaHolbrook et al., 1987; Quinrl et al., VIrLIS

Inducible Elements Element Inducer References MT II Phorbol Ester (TFA) Palmiter et al., 1982;
Haslinger Heavy metals et al., 1985; Searle et al., 1985;

Stuart et al., 1985;
Imagawa et al., 1987, I~arin et al., 1987;

Angel et al., 1987b;
McNeall et al., 1989 MMTV (mouse Glucocorticoids Huang et al., 1981;
Lee et al., mammary tumor 1981; Majors et al., 1983;

virus) Chandler et al., 1983;
Lee et al., 1984; Ponta et al., 1985;

Sakai et al., 1988 (3-Interferon poly(rI)x Tavernier et al., 1983 poly(rc) Adenovirus 5 ElA Imperiale et al., 1984 Collagenase Phorbol Ester (TPA) Angel et al., 1987a Stromelysin Phorbol Ester (TPA) Angel et al., 1987b SV40 Phorbol Ester (TPA) .Angel et al., 1987b Inducible Elements Element Inducer References Murine MX Gene Interferon, NewcastleHug et al., 1988 Disease Virus GRP7S Gene A23187 Resendez et al., 1988 cx-2-MacroglobulinIL-6 Kunz et al., 1989 Vimentin Serum Rittling et al., 1989 MHC Class I Interferon Blanar et al., 1989 Gene H-2,Kb HSP70 , EIA, SV40 Large T Taylor et al., 1989, Antigen 1990a, 1990b Proliferin Phorbol Ester-TPA Mordacq et al., 1989 Tumor Necrosis PMA Hensel et al., 1989 Factor Thyroid StimulatingThyroid Hormone Chatterjee et al., Hormone a Gene 1989 In one aspect, tissue-specific promoters, e.g., cardiac-specific and/or fibroblast-specific promoters, are of particular interest. By way of illustration, cardiac-specific promoters include the myosin light chain-2 promoter (Franz et al., 1994; Kelly et al., 1995), the alpha actin promoter (Moss et al., 1996), the troponin 1 promoter (Bhavsar et°al., 1996); the Na~/Ca2+ exchanger promoter (Barnes et al., 1997), the dystrophin promoter (Kimura et al., 1997), the creatine kinase promoter (Ritchie, M.E., 1996), the alpha? integrin promoter (Ziober & Kramer, 1996), the brain natriuretic peptide promoter (LaPointe et al., 1996) and the alpha B-crystalliWsmall heat shock protein promoter (Gopal-Srivastava, R., 1995), alpha myosin heavy chain promoter (Yamauchi-Takihara et al., 1989) and the ANF
promoter (LaPointe et al., 1988).
Where a cDNA insert is employed, one will typically desire to include a polyadenylation signal to effect proper polyadenylation of the gene transcript. The nature of the polyadenylation signal is not believed to be crucial to the successful practice of the invention, and any such sequence may be employed such as human growth hormone and SV40 polyadenylation signals. Also contemplated as an element of the expression cassette is a terminator. These elements can serve to enhance message levels and to minimize read through from the cassette into other sequences.
(ii) Selectable Markers In certain embodiments of the invention, in which cells contain nucleic acid constructs of the present invention, a cell may be identified in vitro or in vivo by including a marker in the expression construct. Such markers would confer an identifiable change to the cell permitting easy identification of cells containing the expression construct. Usually the inclusion of a drug selection marker aids in cloning and in the selection of transformants, for example, genes that confer resistance to neomycin, puromycin, hygromycin, DHFR, GPT, zeocin and histidinol are useful selectable markers. Alternatively, enzymes such as herpes simplex virus thymidine kinase (tk) or chloramphenicol acetyltransferase (CAT) may be employed.
Immunologic markers also can be employed. The selectable marker employed is not believed to be important, so long as it is capable of being expressed simultaneously with the nucleic acid encoding a gene product. Further examples of selectable markers are well known to one of skill in the art.
(iii) Multigene Constructs and IRES
In certain embodiments of the invention, the use of internal ribosome entry site (IRES) elements are used to create multigene, or polycistronic, messages. IRES
elements is believed to allow bypassing of the ribosome scanning model of 5' methylated Cap dependent translation and facilitate translation at internal sites (Pelletier and Sonenberg, 1988). By way of illustration, IRES elements from two members of the picanovirus family (polio and encephalomyocarditis) have been described (Pelletier and Sonenberg, 1988), as well an IRES from a marmnalian message (Macejak and Sarnow, 1991). IRES elements can be linked to heterologous open reading frames: Multiple open reading frames can be transcribed together, each separated by an IRES, creating polycistronic messages. By virtue of the TRES
element, each open reading frame is accessible to ribosomes for efficient translation.

Multiple genes can be efficiently expressed using a single promoter/enhancer to transcribe a single message.
Any heterologous open reading frame can be linked to IRES elements. This includes genes for secreted proteins, rnulti-subunit proteins, encoded by independent genes, intracellular or membrane-bound proteins and selectable markers. In this way, expression of several proteins can be simultaneously engineered into a cell with a single construct and a single selectable marker.
(iv) Polyadenylation Signals In expression, one will typically include a polyadenylation signal to effect proper polyadenylation of the transcript. The nature of the polyadenylation signal is not believed to be crucial to the successful practice of the invention, and any of a .
number of such sequences may be employed. Exemplary embodiments include the SV40 polyadenylation signal, the bovine growth hormone polyadenylation signal and others which are convenient and/or known to function well in various target cells.
Also contemplated as an element of the expression cassette is a transcriptional termination site. These elements can serve to enhance message levels and/or to minimize read through from the cassette into other sequences.
(v) Vectors The term "vector" is used to refer to carnet molecules with which a nucleic acid sequence can be associated for introduction into a cell. The nucleic acid sequence can be "exogenous," (e.g., foreign to the cell into which it is introduced) or "endogenous" (e.g., the same as a sequence in the cell into which it is introduced.
Exemplary vectors include plasmids, cosmids, viruses (bacteriophage, animal viruses, and plant viruses), and artificial chromosomes (e.g., YACs), lipid-based vectors (e.g., liposomes) and other macromolecular complexes capable of mediating delivery of a polynucleotide to a host cell. One of skill in the art would be well equipped to construct a vector through standard techniques, for example standard recombinant techniques such as described in Sambrook et al., 1989 and Ausubel et al., 1994, both incorporated herein by reference.

A large number of viral and non-viral vectors (including lipid-based and other synthetic delivery systems known in the art) can likewise be employed to deliver polynucleotides of the present invention. Such vectors may be modified, as known to those of skill in the art, to confer or enhance cell specificity. By way of illustration, the surface of viral vectors may be modified such that they preferentially or exclusively bind to and/or infect a particular target cell population.
As used herein, the term "expression vector" refers to a vector containing a nucleic acid sequence coding for at least part of a gene product capable of being transcribed. In some cases, the transcription products) are then translated into a protein, polypeptide, or peptide. In other cases, these sequences are not translated, for example, in the production of antisense molecules or ribozymes. Expression vectors can contain a variety of "control sequences," which refer to nucleic acid sequences that regulate the transcription and possibly translation of an operably linked coding sequence in a particular host organism. In addition to control sequences that govern transcription and translation, vectors and expression vectors may contain nucleic acid sequences that serve other functions as well for example as described infra.
(vi) Host Gells As used herein, the terms "cell," "cell line," and "cell culture" may be used interchangeably. These terms also include their progeny, which is any and all subsequent generations. It is understood that all progeny may not be identical due to deliberate or inadvertent mutations.' In the context of expressing a heterologous nucleic acid sequence, "host cell" refers to a prokaryotic or eukaryotic cell, and. it includes any transformable organisms that is capable of replicating a vector and/or expressing a heterologous gene encoded by a vector. A host cell can, and has been, used as a recipient for vectors. A host cell may be "transfected" or "transformed,"
which refers to a process by which exogenous nucleic acid is transferred or introduced into the host cell. A transformed cell includes the primary subject cell and its progeny.
Some vectors may employ control sequences that allow it to be replicated and/or expressed in both prokaryotic and eukaryotic cells. One of skill in the art would further understand conditions under which to incubate such host cells to maintain them and to permit replication of a vector. Also understood and known are techniques and conditions that would allow large-scale production of vectors, as well.
as production of the nucleic acids encoded by vectors and their cognate polypeptides, .
proteins, or peptides.
(vii) Expression Systems Numerous expression systems exist that comprise at least a part or all of the compositions discussed above. Prokaryote- and/or eukaryote-based systems can be employed for use with the present invention to produce nucleic acid sequences, or their cognate polypeptides, proteins and peptides. Many such systems are commercially and widely available.
The insect cell/baculovirus system can produce a High level of protein expression of a heterologous nucleic acid segment, such as described in U.S.
Patent 5,871,986, 4,879,236, both herein incorporated by reference, and which can be bought, for example, under the name MAXBAC~ 2.0 from INVITROGENO and BACPACI~TM baculovirus expression system from CLONTECH~.
Other examples of expression systems include STRATAGENE~'s COMPLETE CONTROLT"" Inducible Mammalian Expression System, which involves a synthetic ecdysone-inducible receptor, or its pET Expression System, an E.
coli expression system. Another example of an inducible expression system is available from INVITROGENC~, which carries the T-REXTM (tetracycline-regulated expression) System, an inducible mammalian expression system that uses the full-.
length CMV promoter. INVITROGEN~ also provides a yeast expression system called the Pichia methanolica Expression System, which is designed for high-level production of recombinant proteins in the methylotrophic yeast Pichia methanolica.
One of skill in the art would know how to express a vector, such as an expression construct, to produce a nucleic acid sequence or its cognate polypeptide, protein, or peptide.
(viii) Gene Delivery Means There are a number of ways in which a gene of interest, for example within an expression vector, may be introduced into cells. In certain embodiments of the invention, the gene delivery means comprises a virus or engineered construct derived from a viral genome. The ability of certain viruses to enter cells for example via receptor-mediated endocytosis and to express viral genes stably and efficiently have made them attractive candidates for the transfer of foreign genes into mammalian cells (Ridgeway, 1988; Nicolas and Rubenstein, 1988; Baichwal and Sugden, 1986;
Temin, 1986). The first vimses used as gene vectors were DNA viruses including the papovaviruses (simian virus 40, bovine papilloma virus, and polyoma) (Ridgeway, 1988; Baichwal and Sugden, 1986) and adenoviruses (Ridgeway, 1988; Baichwal and Sugden, 1986). Although these viral vectors generally have a relatively fixed capacity for foreign DNA can accornlnodate up to 5-10 kb of foreign DNA and many different viral vectors can be readily introduced into a variety of different cells and animals (see, e.g., Nicolas and Rubenstein, 1988; Temin, 1986). Where viral vectors are employed to deliver the gene or genes of interest, it is generally preferred that they be replication-defective.
One of the preferred methods for in wivo gene delivery involves the use of an adenovirus expression vector. "Adenovirus expression vector" is meant to include those constructs containing adenovims sequences sufficient to (a) support packaging of the construct and (b) to express polynucleotide that has been cloned therein. In this context, expression does not require that the gene product be synthesized.
An adenivorus expression vector comprises a genetically engineered form of adenovirus. Knowledge of the genetic organization of adenovirus, a linear, double-stranded DNA virus, allows substitution of large pieces of adenoviral DNA with foreign sequences (typically up to about 7 kB (Grunhaus and Horwitz, 1992)).
Modified adenoviral and other viral vectors have also been constructed to provide for increased packaging capacity and are likewise contemplated herein. In contrast to retrovirus, the adenoviral infection of host cells does not generally result in chromosomal integration. Also, adenoviruses are structurally stable, and no genome rearrangement has been detected after extensive amplification. Adenovirus can infect various lineages of cells regardless of their cell cycle stage. So far, adenoviral infection appears to be linked only to mild disease such as acute respiratory disease in humans.

Adenovirus is particularly suitable for use as a gene transfer vector because of its mid-sized genome, ease of manipulation, high titer, wide target cell range and high infectivity. In the case of adenovirus serotype 5 (Ad5), for example, both ends of the viral genome contain 100-200 base pair inverted repeats (ITRs), which are cis elements necessary for viral DNA replication and packaging. The early (E) and late (L) regions of the genome contain different transcription units that are divided by the onset of viral DNA replication. The E1 region (ElA and ElB) encodes proteins responsible for the regulation of transcription of the viral genome and a few cellular genes. The expression of the E2 region (E2A and E2B) results in the synthesis of the proteins for viral DNA replication. These proteins are involved in DNA
replication, late gene expression and host cell shut-off (Reran, 1990). The products of the late genes, including the majority of the viral capsid proteins, axe expressed only after significant processing of a single primary transcript issued by the major late promoter (MLP). The MLP (located at 16.8 m.u.) is particularly efficient during the late phase of infection, and the mRNA's issued from this promoter possess a S'-tripartite leader (TPL) sequence which makes them preferred mRNA's for translation.
In one system, recombinant adenovirus is generated from homologous recombination between shuttle vector and provirus vector. Due to the possible recombination between two proviral vectors, wild-type adenovirus may be generated from this process. Therefore, it is important to minimize this possibility by reducing or eliminating adnoviral sequence overlaps within the system and/or to isolate a single clone of virus from an individual plaque and examine its genomic structure.
Generation and propagation of replication-deficient adenovirus vectors depend on a unique helper cell line, such as the human 293 cell line, which was transformed from human embryonic kidney cells by Adenovirus type 5 DNA fragments to constitutively expresses El proteins (Graham et al., 1977). Since the E3 region is dispensable from the adenovirus genome (Jones and Shenk, 1978), the current adenovirus vectors, with the help of 293 cells, generally carry foreign DNA in either the E1, the E3 or both regions (Graham and Prevec, 1991). In nature, adenovirus can package approximately 105% of the wild-type genome (Ghosh-Choudhury et al., 1987), providing capacity for about 2 extra kb of DNA. Combined with the approximately 5.5 kb of DNA that is replaceable in the E 1 and E3 regions, up to about 7.5 kb of foreign DNA may be packaged in an adenovirus. Additionally, modified adenoviral vectors are now available which have an even greater capacity to carry foreign DNA.
Helper cell lines may be derived from human. cells such as human embryonic kidney cells, muscle cells, hematopoietic cells or other human embryonic mesenchymal or epithelial cells. Alternatively, the helper cells may be derived from the cells of other mammalian species that are permissive for human adenovirus.
Such cells include, e.g., Vero cells or other monkey embryonic mesenchymal or epithelial cells. As stated above, a preferred helper cell line is 293.
Racher et al. (1995) disclosed improved methods for culturing 293 cells and propagating adenovirus: In one format, natural cell aggregates are grown by inoculating individual cells into 1 liter siliconized spinner flasks (Techne, Cambridge, UK) containing 100-200 ml of medium. Following stirnng at 40 rpm, the cell viability is estimated with trypan blue. In another format, Fibra-Cel microcarriers (Bibby Sterlin, Stone, UK) (5 g/1) are employed as follows. A cell inoculum, resuspended in 5 ml of medium, is added to the carrier (50 ml) in a 250: ml Erlenmeyer flask and left stationary, with occasional agitation, for 1 to 4 h.
The medium is then replaced with 50 ml of fresh medium and shaking initiated. For virus production, cells are allowed to grow to about 80% confluence, after which time the medium is replaced (to 25% of the final volume) and adenovirus added at an MOI
of 0.05. Cultures are left stationary overnight, following which the volume is increased to 100% and shaking commenced for another 72 h.
Other than the preference that the adenovirus vector be replication-defective, or at least conditionally defective, the nature of the adenovirus vector is not believed to be critical to the successful practice of the invention. The adenovirus may be selected from any of the 42 different known serotypes or subgroups A-F.
Adenovirus serotype 5 of subgroup C is a preferred starting material for obtaining a conditional replication-defective adenovirus vector for use in the present invention. This is, in part, because Adenovirus type 5 is a human adenovirus about which a great deal of biochemical and genetic information is known, and it has historically been used for most constructions employing adenovirus as a vector. Additionally, various modifications can be made to. adenovirus to facilitate cell targeting of the expression cassette and/or otherwise modify vector interaction with the host cell. By way of illustration, it is known that primary fibroblasts generally express low levels of the high-affinity Coxsackie virus and Adenovirus receptor (CAR), which receptor facilitates transduction of host cells by the adenoviral vector. However, it is also known that adenoviral vectors can be modified, for example by altering the adenovirus fiber, to improve binding to other cell-surface receptors where CAR
receptors are limited (see, e.g. Hidaka et al., 1999).
As stated above, a preferred adenoviral vector according to the present invention lacks an adenovirus E1 region and thus, is replication defective.
Typically, it is most convenient to introduce the polynucleotide encoding the gene of interest at the position from which the E1-coding sequences have been removed. However, the position of insertion of the construct within the adenovirus sequences is not critical to the invention. Further, other adenoviral sequences may be deleted and/or inactivated in addition to or in lieu of the El region. For example, the E2 and E4 regions are both necessary for adenoviral replication and thus may be modified to render an adenovirus vector replication-defective, in which case a helper cell Iine or helper virus complex may employed to provide such deleted/inactivated genes isz t~as2,r. The polynucleotide encoding the gene of interest may alternatively be inserted in lieu of a deleted E3 region, such as in E3 replacement vectors as described by Karlsson et al.
(1986), or in the E4 region where a helper cell line or helper virus complements an E4.
defect.
Other modifications are known to those of skill in the art and are likewise contemplated herein.
Adenovirus is easy to grow and manipulate and exhibits broad host range in vitro and in vivo. This group of viruses can be obtained in high titers, e.g., 109-lOlz plaque-forming units per ml, and they are highly infective. The life cycle of adenovirus does not require integration into the host cell genome. The foreign genes delivered by adenovirus vectors are episomal and, therefore, have low genotoxicity to host cells. No side effects have been reported in studies of vaccination with wild-type adenovirus (Couch et al., 1963; Top et al., 1971), demonstrating their safety and therapeutic potential as in vivo gene transfer vectors.

Adenovirus vectors have been used in eukaryotic gene expression (Levrero et al., 1991; Gomez-Foix et al., 1992) and vaccine development (Grunhaus and Horwitz, 1992; Graham and Prevec, 1991). Animal studies initially suggested that recombinant adenovirus could be useful for gene therapy (see, e.g., Stratford-Perricaudet and Perricaudet, 1991; Stratford-Perricaudet et al:, 1990; Rich et al., 1993).
Studies in administering recombinant adenovirus to different tissues include administration via intracoronary catheter into one or more coronary arteries of the heart (Hammond, et al.), U.S. Patents 5,792,453 and 6,100,242), trachea instillation (Rosenfeld et al:, 1991; Rosenfeld et al., 1992), muscle injection (Ragot et al., 1993), peripheral intravenous injections (Herz and Gerard, 1993) and stereotactic inoculation into the brain (Le Gal La Salle et al., 1993).
The retroviruses are a group of single-stranded RNA viruses characterized by an ability to convert their RNA to double-stranded DNA in infected cells by a process of reverse-transcription (Coffin, 1990). The resulting DNA then stably integrates into cellular chromosomes as a provirus and directs synthesis of viral proteins.
The integration results in the retention of the viral gene sequences in the recipient cell and its descendants. The retroviral genome contains three genes, gag, pol, and env that code for capsid proteins, polymerase enzyme, and envelope components, respectively.
A sequence found upstream from the gag gene contains a signal for packaging of the genome into virions. Two long terminal repeat (LTR) sequences are present at the 5' and 3' ends of the viral genome. These contain strong promoter and enhancer sequences and are also required for integration in the host cell genome (Coffin, 1990).
In order to construct a retroviral vector, a nucleic acid encoding a gene of interest is inserted into the viral genome in the place of certain viral sequences to produce a virus that is replication-defective. In order to produce virions, a packaging cell line containing the gag, pol, and env genes but without the LTR and packaging components is generally employed (Mann et al., 1983). When a recombinant plasmid containing a cDNA, together with the retroviral LTR and packaging sequences is introduced into this cell line (by calcium phosphate precipitation for example), the packaging sequence allows the RNA transcript of the recombinant plasmid to be packaged into viral particles, which are then secreted into the culture media (Nicolas and Rubenstein, 1988; Temin, 1986; Main et al., 1983). The media containing the recombinant retroviruses is then collected, optionally concentrated, and used for gene transfer. Retroviral vectors are able to infect a broad variety of cell types.
However, integration and stable expression require the division of host cells (Paskind et al., 1975).
A novel approach designed to allow specific targeting of retrovinxs vectors was recently developed based on the chemical modification of a retrovirus by the chemical addition of lactose residues to the viral envelope. This modification could permit the specific infection of hepatocytes via sialoglycoprotein receptors.
A different approach to targeting of recombinant retrovinises was designed in which biotinylated antibodies against a retroviral envelope protein and against a specific cell receptor were used. The antibodies were coupled via the biotin components by using streptavidin (Roux et al., 1989). Using antibodies against major histocompatibility complex class I and class II antigens, they demonstrated the infection of a variety of human cells that bore those surface antigens with an ecotropic virus iTZ vitro (Roux et al., 1989).
There are certain limitations to the use of retrovirus. For example, retrovirus vectors usually integrate into random sites in the cell genome. This can lead to insertional rnutagenesis through the interruption of host genes or through the insertion of viral regulatory sequences that can interfere with the function of flanking genes (Varmus et al., 1981).' Another concern with the use of defective retrovinis vectors is the potential appearance of wild-type replication-competent virus in the packaging cells. This can result from recombination events in which the intact-sequence from the recombinant virus inserts upstream from the gag, pol, env sequence integrated in the host cell genome. However, new packaging cell lines are now available that should greatly decrease the likelihood of recombination (Markowitz et al., 1988;
Hersdorffer et al., 1990).
Other viral vectors may be employed as expression constructs in the present invention. Vectors derived from viruses such as vaccinia virus (Ridgeway, 1988;
Baichwal and Sugden, 1986; Coupar et al., 1988) adeno-associated virus (AAV) (Ridgeway, 1988; Baichwal and Sugden, 1986; Hermonat and Muzycska, 1984) and herpesviruses may be employed. They offer several attractive features fox various mammalian cells (Friedmann, 1989; Ridgeway; 1988; Baichwal and Sugden, 1986;
Coupar et al., 1988; Norwich et al., 1990).
With the recent recognition of defective hepatitis B viruses, new insight was gained into the structure-function relationship of different viral sequences.
Ih vitro studies showed that the virus could retain the ability for helper-dependent packaging and reverse transcription despite the deletion of up to 80% of its genome (Norwich et al., 1990). This suggested that large portions of the genorne could be replaced with foreign genetic material. The hepatotropism and persistence (integration) were particularly attractive properties for liver-directed gene transfer. Chang et al., recently introduced the chloramphenicol acetyltransferase (CAT) gene into duck hepatitis B
virus genome in the place of the polymerise, surface, and pre-surface coding sequences. It was co-transfected with wild-type virus into an avian hepatoma cell line. Culture media containing high titers of the recombinant virus were used to infect primary duckling hepatocytes. Stable CAT gene expression was detected for at least 24 days after transfection (Chang et al., 1991).
In order to effect expression of sense or antisense gene constructs, the expression construct is delivered into a cell. This delivery may be accomplished ih vitro, as in laboratory procedures for transforming cells lines, or ih vivo or ex vivo, as in the treatment of certain disease states. One mechanism for delivery is via viral infection where the expression construct is encapsidated in an infectious viral particle.
Non-viral methods for the transfer of expression constructs into mammalian cells can also be used in the context of the present invention. These include calcium phosphate precipitation (Graham and Van Der Eb, 1973; Chen and Okayama, 1987;
Rippe et al., 1990) DEAF-dextrin (Gopal, 1985), electroporation (Tur-Kaspa et al., 1986; Potter et al., 1984), direct microinjection (Harland and Weintraub, 1985), DNA-loaded liposomes (Nicolau and Sene, 1982; Fraley et al., 1979) and lipofectamine-DNA complexes, cell sonication (Fechheimer et al., 1987), gene bombardment using high velocity microprojectiles (Yang et al., 1990), and receptor-mediated transfection (Wu and Wu, 1987; Wu and Wu, 1988). Some of these techniques may be successfully adapted for in vivo or ex vivo use.

Once the expression construct has been delivered into the cell the nucleic acid encoding the gene of interest may be positioned and expressed at different sites. In certain embodiments, the nucleic acid encoding the gene may be stably integrated into the genome of the cell. This integration may be in the cognate location and orientation via homologous recombination (gene replacement) or it may be integrated in a random, non-specific location (gene augmentation). In yet further embodiments, the nucleic acid may be stably maintained in the cell as a separate, episomal segment of DNA. Such nucleic acid segments or "episomes" encode sequences sufficient to permit maintenance and replication independent of or in synchronization with the host cell cycle. How the expression construct is delivered to a cell and where in the cell .
the nucleic acid remains is dependent on the type of expression construct employed.
In yet another embodiment of the invention, the expression construct may simply consist of naked recombinant DNA or plasmids. Transfer of the construct may be performed by any of the methods mentioned above which physically or chemically permeabilize the cell membrane. This is particularly applicable for transfer in vitro but it may be applied to in vivo use as well. Dubensky et al. (1984) successfully injected polyomavirus DNA in the form of calcium phosphate precipitates into liver and spleen of adult and newborn mice demonstrating active viral replication and acute infection. Benvenisty and Neshif (1986) also demonstrated that direct intraperitoneal injection of calcium phosphate-precipitated plasmids results in expression of the transfected genes. It is envisioned that DNA encoding a gene of interest may also be transferred in a similar manner in vivo and express the gene product.
In still another embodiment of the invention, a naked DNA expression construct may be transferred into cells using particle bombardment. This method depends on the ability to accelerate DNA-coated microprojectiles to a high velocity allowing them to pierce cell membranes and enter cells without killing them (Klein et al., 1987). Several devices for accelerating small particles have been developed. One such device relies on a high voltage discharge to generate an electrical current, which in turn provides the motive force (Yang et al., 1990). The microprojectiles used have consisted of biologically inert substances such as tungsten or gold beads.

Selected organs including the liver, skin, and muscle tissue of rats and mice have been bombarded iri vivo (Yang et al., 1990; Zelenin et al., 1991). This may require surgical exposure of the tissue or cells, to eliminate any intervening tissue between the gun and the target organ, i.e., ex vivo treatment. Again, DNA
encoding a particular gene may be delivered via this method and still be incorporated by the presentinvention.
In a further embodiment of the invention, the expression construct may be complexed with one or more lipid components and/or entrapped in a liposome.
Liposomes are vesicular structures characterized by a phospholipid bilayer membrane and an inner aqueous medium. Multilamellar liposomes have multiple lipid layers separated by aqueous medium. They form spontaneously when phospholipids are suspended in an excess of aqueous solution. The lipid components undergo self rearrangement before the formation of closed structures and entrap water and dissolved solutes between the lipid bilayers (Ghosh and Bachhawat, 1991). Also contemplated are lipofectamine-DNA complexes.
Liposome-mediated nucleic acid delivery and expression of foreign DNA in vitro has been very successful. Wong et al., (1980) demonstrated the feasibility of liposome-mediated delivery and expression of foreign DNA in cultured chick embryo, HeLa and hepatoma cells. Nicolau et al., (1987) accomplished successful liposome-mediated gene transfer in rats after intravenous injection.
In certain embodiments of the invention, the liposome may be complexed with a hemagglutinating virus (HVJ). This has been shown to facilitate fusion with the cell membrane and promote cell entry of liposome-encapsulated DNA (Kaneda et al., 1989). In other embodiments, the liposome may be complexed or employed in conjunction with nuclear non-histone chromosomal proteins (HMG-1) (Kato et al., 1991 ). In yet further embodiments, the liposome may be complexed or employed in conjunction with both HVJ and HMG-1. In that such expression constructs have been successfully employed in transfer and expression of nucleic acid in vitro and in vivo, then they are applicable for the present invention. Where a bacterial promoter is employed in the DNA construct, it also will be desirable to include within the liposome an appropriate bacterial polymerase.

Other expression constructs which can be employed to deliver a nucleic acid encoding a particular gene into cells are receptor-mediated delivery vehicles.
These take advantage of the selective uptake of macromolecules by receptor-mediated endocytosis in most eukaryotic cells. Because of the cell type-specific distribution of various receptors, the delivery can be highly specific (Wu and Wu, 1993).
Receptor-mediated gene targeting vehicles generally consist of two components: a cell receptor-specific ligand and a DNA-binding agent. Several ligands have been used for receptor-mediated gene transfer. The most extensively characterized ligands are asialoorosomucoid (ASOR) (Wu and Wu, 1987) and transferrin (Wagner et al., 1990). Recently, a synthetic neoglycoprotein, which recognizes the same receptor as ASOR, has been used as a gene delivery vehicle (Ferkol et al., 1993; Perales et al., 1994) and epidermal growth factor (EGF) has also been used to deliver genes to squamous carcinoma cells (Myers, EPO 0273085).
In other embodiments, the delivery vehicle may comprise a ligand and a liposome. For example, Nicolau et al., (1987) employed lactosyl-ceramide, a galactose-terminal asialganglioside, incorporated into liposomes and observed an increase in the uptake of the insulin gene by hepatocytes. Thus, it is feasible that a nucleic acid encoding a particular gene also may be specifically delivered into a cell type by any number of receptor-ligand systems with or without liposomes. For example, epidermal growth factor (EGF) may be used as the receptor for mediated delivery of a nucleic acid into cells that exhibit upregulation of EGF
receptor.
Mannose can be used to target the mannose receptor on liver cells. Also, antibodies to CDS (CLL), CD22 (lymphoma), CD25 (T-cell leukemia) and MAA (melanoma) can similarly be used as targeting moieties.
In certain embodiments, gene transfer may more easily be performed under ex vivo conditions. Ex vivo gene therapy refers to the isolation of cells from an animal, the delivery of a nucleic acid into the cells in vitro, and then the return of the modified cells back into an animal. This may involve the surgical removal of tissue/organs from an animal or the primary culture of cells and tissues.

II. Myocardin Peptides and Polypeptides The present invention also provides exemplary myocardin protein/polypeptide sequences. For example, SEQ ID NOS:2, 26, 28 and 30 provide amino acid sequences for myocardins of SEQ ID NOS:1, 25, 27 and 29, respectively. In addition to entire myocardin molecules, the present invention also relates to fragments of the polypeptides that may or may not retain the various functions described below.
By way of illustration, N-terminally truncated myocardin 1 polypeptides from mouse and human (SEQ ID NOS: 2 and 26, respectively) are provided, which polypeptides retain the various functions described below. Fragments, including the N-terminus of the molecule may be generated by genetic engineering of translation stop sites within the coding region (discussed below). Alternatively, treatment of the polypeptides with proteolytic enzymes, known as proteases, can produces a variety of N-terminal, C-terminal and internal fragments. These fragments may be purified according to known methods, such as pr.;cipitation (e.g., ammonium sulfate), HPLC, ion exchange chromatography, affinity chromatography (including immunoaffinity chromatography) or various size separations (sedimentation, gel electrophoresis, gel filtration).
A. Structural and Functional Aspects Myocardin 1 from human and mouse, shown in SEQ ID N0:28 and SEQ ID
N0:30 are 935 and 938 residues, respectively. In human myocardin 1, the nuclear localization sequence (NLS) is located between residues 245 and 254, within a basic region at residues 243-260. A glutamine-rich (Q) domain is located between residues 287-320. The SAP domain is found at residues 380-414. The transcription activation domain is located at the carboxyl-terminus at 670 to 935.
In general, myocardins are cell regulatory proteins/peptides that function to modulate cell phenotype. In particular, myoeardin can be used to reduce the deleterious effects of non-cardiomyocytes on injured myocardium and/or to stimulate non-cardiomyoeytes to perform one or more functions typical of cardiomyocytes, thereby enhancing cardiac function. By way of illustration, myocardin 1 is a novel cardiac-specific regulatory protein capable of modulating the phenotype of target cells within the heart, such as fibroblasts. Overexpression of myocardin 1 in fibroblasts is sufficient to activate expression of a variety of cardiac promoters, including a-myosin heavy chain, atrial natriuretic factor, Nkx2.5 and SM22. In combination with GATA4, myocardin 1 transactivates regulatory sequences in the cardiac specific homeobox Nkx2.5 gene. In addition myocardin 1 is a potent inhibitor of cell proliferation, demonstrated by a reduced number of transfected cells expressing myocardin 1 compared to those expressing a control marker gene. Further, though inhibitory of cell proliferation, myocardin appears to stimulate cardiomyocyte hypertrophy. These results may provide an explanation for the post-mitotic feautures of the cardiomyocytes.
B. Variants of Myocardin Amino acid sequence variants of a myocardin polypeptide can be substitutional, insertional or deletion variants. Deletion variants lack one or more residues of the native protein which are not essential for function or immunogenic activity, and are exemplified by the variants lacking a transmembrane sequence described above. Another common type of deletion variant is one lacking secretory signal sequences or signal sequences directing a protein to bind to a particular part of a cell. Insertional mutants typically involve the addition of material at a non-terminal point in the polypeptide.
This may include the insertion of an immunoreactive epitope or simply a single residue.
Terminal additions, called fusion proteins, are discussed below.
Substitutional variants typically contain the exchange of one amino acid for another at one or more sites within the protein, and may be designed to modulate one or more properties of the polypeptide, such as stability against proteolytic cleavage, without the loss of other functions or properties. Substitutions of this kind preferably are conservative, that is, one amino acid is replaced with one of similar shape and charge.
Conservative substitutions are well known in the art and include, for example, the changes of alanine to serine; arginine to lysine; asparagine to glutamine or histidine;
aspartate to glutamate; cysteine to serine; glutamine to asparagine; glutamate to aspartate; glycine to proline; histidine to asparagine or glutamine;
isoleucine to leucine or valine; leucine to valine or isoleucine; lysine to arginine; methionine to leucine or isoleucine; phenylalanine to tyrosine, leucine or methionine; serine to threonine;

threonine to serine; tryptophan to tyrosine; tyrosine to tryptophan or phenylalanine; and valine to isoleucine or leucine.
The following is a discussion based upon changing of the amino acids of a protein to create an equivalent, or even an improved, second-generation molecule. For example, certain amino acids may be substituted for other amino acids in a protein structure without appreciable loss of interactive binding capacity with structures such as, for example, antigen-binding regions of antibodies or binding sites on substrate molecules. Since it is the interactive capacity and nature of a protein that defines that protein's biological functional activity, certain amino acid substitutions can be made in a protein sequence, and its underlying DNA coding sequence, and nevertheless obtain a protein with like properties. It is thus contemplated by the inventors that various changes may be made in the DNA sequences of genes without appreciable loss of their biological utility or activity, as discussed below. Table 1 shows the codons that encode particular amino acids.
In making such changes, the hydropathic index of amino acids may be considered. The importance of the hydropathic amino acid index in conferring interactive biologic function on a protein is generally understood in the art (Kyle and Doolittle, 1982). It is accepted that the relative hydropathic character of the amino acid contributes to the secondary structure of the resultant protein, which in turn defines the interaction of the protein with other molecules, for example, enzymes, substrates, receptors, DNA, antibodies, antigens, and the like. .
Each amino acid has been assigned a hydropathic index on the basis of their hydrophobicity and charge characteristics (Kyle and Doolittle, 1982), these are:
isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8);
cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine (-0.4); threonine (-0.7);
serine (-0.8); tryptophan (-0.9); tyrosine (-1.3); proline (-1.6); histidine (-3.2);
glutamate (-3.5); glutamine (-3.5); aspartate (-3.5); asparagine (-3.5); lysine (-3.9);
and arginine (-4.5).
It is known in the art that certain amino acids may be substituted by other amino acids having a similar hydropathic index or score and still result in a protein with similar biological activity, i.e., still obtain a biological functionally equivalent protein. In making such changes, the substitution of amino acids whose hydropathic indices are within ~2 is preferred, those which are within +1 are particularly preferred, and those within +0.5 are even more particularly preferred.
It is also understood. in the art that the substitution of like amino acids can be made effectively on the basis of hydrophilicity. U.S. Patent 4,554,101, incorporated herein by reference, states that the greatest local average hydrophilicity of a protein, as governed by the hydrophilicity of its adjacent amino acids, correlates with a biological property of the protein. As detailed in U.S. Patent 4,554,101, the following hydrophilicity values have been assigned to amino acid residues: arginine (+3.0);
lysine (+3.0); aspartate (+3.0 ~ 1); glutamate (+3.0 ~ 1); serine (+0.3);
asparagine (+0.2); glutamine (+0.2); glycine (0); threonine (-0.4); proline (-0.5 ~ 1);
alanine (-0.5); histidine *-0.5); cysteine (-1.0); methionine (-1.3); valine (-1.5);
leucine (-1.8);
isoleucine (-1.8); tyrosine (-2.3); phenylalanine (-2.5); tryptophan (-3.4).
It is understood that an amino acid can be substituted for another having a similar hydrophilicity value and still obtain a biologically equivalent and immunologically equivalent protein. :fn such changes, the substitution of amino acids whose hydrophilicity values are within ~2 is preferred, those that are within ~1 are particularly preferred, and those within X0.5 are even more particularly preferred.
As outlined above, amino acid substitutions are generally based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skill in the art and include: arginine and lysine; glutamate and aspartate; serine and threonine;
glutamine and asparagine; and valine, leucine and isoleucine.
Another embodiment for the preparation of polypeptides according to the invention is the use of peptide mimetics. Mimetics are peptide-containing molecules that mimic elements of protein secondary structure (Johnson et al, 1993). The underlying rationale behind the use of peptide mimetics is that the peptide backbone of proteins exists chiefly to orient amino acid side chains in such a way as to facilitate molecular interactions, such as those of antibody and antigen. A peptide mimetic is expected to permit molecular interactions similar to the natural molecule.
These principles may be used, in conjunction with the principles outline above, to engineer second generation molecules having many. of the natural properties of myocardin, but with altered and even improved characteristics.
C. Domain Switching Domain switching involves the generation of chimeric molecules using different but, in this case, related polypeptides. By comparing various myocardin proteins, one can make predictions as to the functionally significant regions of these molecules. It is possible, then, to switch related domains of these molecules in an effort to determine the criticality of these regions to myocardin function.
These molecules may have additional value in that these "chimeras" can be distinguished from natural molecules, while possibly providing the same function. In particular, it is contemplated that one will create chimeras between myocardins, for example, between myocardin 1 & myocardin 2, myocardinl & myocardin 3, myocardin 2 &
myocardin 3, and/or myocardin 1, myocardin 2 & myocardin 3.
D. Fusion Proteins A specialized kind of insertional variant is the fusion protein. This molecule generally has all or a substantial portion of the native molecule linked, at the N- or C-terminus, to all or a portion of a second polypeptide. For example, fusions typically employ leader sequences from other species to permit the recombinant expression of a protein in a heterologous host. Another useful fusion includes the addition of a immunologically active domain, such as an antibody epitope, to facilitate purification of the fusion protein. Inclusion of a cleavage site at or near the fusion junction will facilitate removal of the extraneous polypeptide after purification. Other useful fusions include linking of functional domains, such as active sites from enzymes, glycosylation domains, cellular targeting signals or transmembrane regions.

E. Purification of Proteins It may be desirable to purify myocardin or variants thereof. Protein purification techniques are well known to those of skill in the art. These techniques involve, at one level, the crude fractionation of the cellular milieu to polypeptide and non-polypeptide fractions. Having separated the polypeptide from other proteins, the polypeptide of interest may be further purified using chromatographic and electrophoretic techniques to achieve partial or complete purification (or purification to homogeneity). Analytical methods particularly suited to the preparation of a pure peptide are ion-exchange chromatography, exclusion chromatography;
polyacrylamide gel electrophoresis; isoelectric focusing. A particularly efficient method of purifying peptides is fast protein liquid chromatography or even HPLC.
Certain aspects of the present invention concern the purification, and in particular embodiments, the substantial purification, of an encoded protein or peptide.
The term "purified protein or peptide" as used herein, is intended to refer to a composition, isolatable from other components, wherein the protein or peptide is purified to any degree relative to its naturally-obtainable state. A purified protein or peptide therefore also refers to a protein or peptide, free from the environment in which it may naturally occur.
Generally, "purified" will refer to a protein or peptide composition that has been subjected to fractionation to remove various other components, and which composition substantially retains its expressed biological activity. Where the term "substantially purified" is used, this designation will refer to a composition in which the protein or peptide forms the major component of the composition, such as constituting about 50%, about 60%, about 70%, about 80%, about 90%, about 95%
or more of the proteins in the composition.
Various methods for quantifying the degree of purification of the protein or peptide will be known to those of skill in the art in light of the present disclosure.
These include, for example, determining the specific activity of an active fraction, or assessing the amount of polypeptides within a fraction by SDS/PAGE analysis. A
preferred method for assessing the purity of a fraction is to calculate the specific activity of the fraction, to compare it to the specific activity of the initial extract, and to thus calculate the degree of purity, herein assessed by a "-fold purification number." The actual units used to represent the amount of activity will, of course, be dependent upon the particular assay technique chosen to follow the purification and whether or not the expressed protein or peptide exhibits a detectable activity.
Various techniques suitable for use in protein purification will be well known to those of skill in the art. These include, for example, precipitation with ammonium sulphate, PEG, antibodies and the like or by heat denaturation, followed by centrifugation; chromatography steps such as ion exchange, gel filtration, reverse phase, hydroxylapatite and affinity chromatography; isoelectric focusing; gel electrophoresis; and combinations of such and other techniques. As is generally known in the art, it is believed that the order of conducting the various purification steps may be changed, or that certain steps may be omitted, and still result in a suitable method for the preparation of a substantially purified protein or peptide.
There is no general requirement that the protein or peptide always be provided in their most purified state. Indeed, it is contemplated that less substantially purified products will have utility in certain embodiments. Partial purification may be accomplished by using .fewer purification steps in combination, or by utilizing different forms of the same general purification scheme. For example, it is appreciated that a canon-exchange column chromatography performed utilizing an HPLC apparatus will generally result in a greater "-fold" purification than the same technique utilizing a low pressure chromatography system. Methods exhibiting a lower degree of relative purification may have advantages in total recovery of protein product, or in maintaining the activity of an expressed protein.
It is known that the migration of a polypeptide can vary, sometimes significantly, with different conditions of SDSlPAGE (Capaldi et al., 1977).
It will therefore be appreciated that under differing electrophoresis conditions, the apparent molecular weights of purified or partially purified expression products may vary.
High Performance Liquid Chromatography (HPLC) is characterized by a very rapid separation with extraordinary resolution of peaks. This is achieved by the use of very fine particles and high pressure to maintain an adequate flow rate.
Separation can be accomplished in a matter of minutes, or at most an hour. Moreover, only a very small volume of the sample is needed because the particles are so small and close-packed that the void volume is a very small fraction of the bed volume.
Also, the concentration of the sample need not be very great because the bands are so narrow that there is very little dilution of the sample.
Gel chromatography, or molecular sieve chromatography, is a special type of partition chromatography that is based on molecular size. The theory behind gel chromatography is that the column, which is prepared with tiny particles of an inert substance that contain small pores, separates larger molecules from smaller molecules as they pass through or around the pores, depending on their size. As long as the material of which the particles are made does not adsorb the molecules, the sole factor determining rate of flow is the size. Hence, molecules are eluted from the column in decreasing size, so long as the shape is relatively constant. Gel chromatography is unsurpassed for separating molecules of different size because separation is independent of other factors such as pH, ionic strength, temperature, etc.
There also is virtually no adsorption, less zone spreading and the elution volume is related in a simple matter to molecular weight.
Affinity Chromatography is a chromatographic procedure that relies on the specific affinity between a substance to be isolated and a molecule that it can specifically bind to. This is a receptor-ligand type interaction. The column material is synthesized by covalently coupling one of the binding partners to an insoluble matrix.
The column material is then able to specifically adsorb the substance from the solution. Elution occurs by changing the conditions to those in which binding will not occur (alter pH, ionic strength, temperature, etc.).
A particular type of affinity chromatography useful in the purification of carbohydrate containing compounds is lectin affinity chromatography. Lectins are a class of substances that bind to a variety of polysaccharides and glycoproteins.
Lectins are usually coupled to agarose by cyanogen bromide. Conconavalin A
coupled to Sepharose was the first material of this sort to be used and has been widely used in the isolation of polysaccharides and glycoproteins other lectins that have been include lentil lectin, wheat germ agglutinin which has been useful in the purification of N-acetyl glucosaminyl residues and Helix pomatia lectin. Lectins themselves are purified using affinity chromatography with carbohydrate ligands. Lactose has been used to purify lectins from castor bean and peanuts; maltose has been useful in extracting lectins from lentils and jack bean; N-acetyl-D galactosamine is used for purifying lectins from soybean; N-acetyl glucosaminyl binds to lectins from wheat germ; D-galactosamine has been used in obtaining lectins from clams and L-fucose will bind to lectins from lotus.
The matrix should be a substance that itself does not adsorb molecules to any significant extent and that has a broad range of chemical, physical and thermal stability. The ligand should be coupled in such a way as to not affect its binding properties. The ligand should also provide relatively tight binding. And it should be possible to elute the substance without destroying the sample or the ligand.
One of the most common forms of affinity chromatography is immunoaffmity chromatography. The generation of antibodies that would be suitable for use in accord with the present invention is discussed below.
F. Synthetic Peptides The present invention also includes smaller myocardin-related peptides for use in various embodiments of the present invention. Because of their relatively small size, the peptides of the invention can also be synthesized in solution or on a solid support in accordance with conventional techniques. Various automatic synthesizers are commercially available and can be used in accordance with known protocols.
See, for example, Stewart and Young (1984); Tam et al. (1983); Mernfield (1986);
and Barany and Mernfield (1979), each incorporated herein by reference. Short peptide sequences, or libraries of overlapping peptides, usually from about 6 up to about 35 to 50 amino acids, which correspond to the selected regions described herein, can be readily synthesized and then screened in screening assays designed to identify reactive peptides. Alternatively, recombinant DNA technology may be employed wherein a nucleotide sequence which encodes a peptide of the invention is inserted into an expression vector, transformed or transfected into an appropriate host cell and cultivated under conditions suitable for expression.

G. Antigen Compositions The present invention also provides for the use of myocardin proteins or peptides as antigens for the immunization of animals relating to the production of antibodies. It is envisioned that myocardin or portions thereof, will be coupled, bonded, bound, conjugated or chemically-linked to one or more agents via linkers, polylinkers or derivatized amino acids. This may be performed such that a bispecific or multivalent composition or vaccine is produced. It is further envisioned that the methods used in the preparation of these compositions will be familiar to those of skill in the art and should be suitable for administration to animals, i.e., pharmaceutically acceptable. Preferred agents are the carriers are keyhole limpet hemocyannin (KLH) or bovine serum albumin (BSA).
III. Generating Antibodies Reactive With Myocardin In another aspect, the present invention contemplates an antibody that is immunoreactive with a myocardin molecule of the present invention, or any portion thereof. An antibody can be a polyclonal or a monoclonal antibody. In a preferred embodiment, an antibody is a monoclonal antibody. Means for preparing and characterizing antibodies are well known in the art (see, e.g., Harlow and Lane, 1988).
Briefly, a polyclonal antibody is prepared by immunizing an animal with an immunogen comprising a polypeptide of the present invention and collecting antisera from that immunized animal. A wide range of animal species can be used for the production of antisera. Typically an animal used for production of anti-antisera is a non-human animal including rabbits, mice, rats, hamsters, pigs or horses.
Because of the relatively large blood volume of rabbits, a rabbit is a preferred choice for production of polyclonal antibodies.
Antibodies, both polyclonal and monoclonal, specific for isoforms of antigen may be prepared using conventional immunization techniques, as will be generally known to those of skill in the art. A composition containing antigenic epitopes of the compounds of the present invention can be used to immunize one or more experimental animals, such as a rabbit or mouse, which will then proceed to produce specific antibodies against the compounds of the present invention. Polyclonal antisera may be obtained, after allowing time for antibody generation, simply by bleeding the animal and preparing serum samples from the whole blood.
It is proposed that the monoclonal antibodies of the present invention will find useful application in standard immunochemical procedures, such as ELISA and Western blot methods and in immunohistochemical procedures such as tissue staining, as well as in other procedures which may utilize antibodies specific to myocardin-related antigen epitopes. Additionally, it is proposed that monoclonal antibodies specific to the particular myocardin of different species may be utilized in other useful applications In general, both polyclonal and monoclonal antibodies against myocardin may be used in a variety of embodiments. For example, they may be employed in antibody cloning protocols to obtain cDNAs or genes encoding other myocardin. They may also be used in inhibition studies to analyze the effects of myocardin-related peptides in cells or animals. Myocardin antibodies will also be useful in immunolocalization studies to analyze the distribution of myocardins during various cellular events, for example, to determine the cellular or tissue-specific distribution of myocardin polypeptides at different points in the cell cycle. A particularly useful application of such antibodies is in purifying native or recombinant myocardin, for example, using an antibody affinity column. The operation of such immunological techniques will be known to those of skill in the art in light of the present disclosure.
Means for preparing and characterizing antibodies are well known in the art (see, e.g., Harlow and Lane, 1988; incorporated herein by reference). More specific examples of monoclonal antibody preparation are given in the examples below.
As is well known in the art, a given composition may vary in its immunogenicity. It is often necessary therefore to boost the host immune system, as may be achieved by coupling a peptide or polypeptide immunogen to a carrier.
Exemplary and preferred Garners are keyhole limpet hemocyanin (KLH) and bovine serum albumin (BSA). Other albumins such as ovalbumin, mouse serum albumin or rabbit serum albumin can also be used as carriers. Means for conjugating a polypeptide to a carrier protein are well known in the art and include glutaraldehyde, m-maleimidobencoyl-N-hydroxysuccinimide ester, carbodiimide and bis-biazotized benzidine.
As also is well known in the art, the immunogenicity of a particular immunogen composition can be enhanced by the use of non-specific stimulators of the immune response, known as adjuvants. Exemplary and preferred adjuvants include complete Freund's adjuvant (a non-specific stimulator of the immune response containing killed Mycobacterium tuberculosis), incomplete Freund's adjuvants and aluminum hydroxide adjuvant.
The amount of immunogen composition used in the production of polyclonal antibodies varies upon the nature of the immunogen as well as the animal used for immunization. A variety of routes can be used to administer the immunogen (subcutaneous, intramuscular, intradermal, intravenous and intraperitoneal).
The production of polyclonal antibodies may be monitored by sampling blood of the immunized animal at various points following immunization. A second, booster, injection may also be given. The process of boosting and titering is repeated until a suitable titer is achieved. When a desired level of immunogenicity is obtained, the immunized animal can be bled and the serum isolated and stored, and/or the animal can be used to generate mAbs.
MAbs may be readily prepared through use of well-known techniques, such as those exemplified in U.S. Patent 4,196,265, incorporated herein by reference.
Typically, this technique involves immunizing a suitable animal with a selected immunogen composition, e.g., a purified or partially purified MCIP protein, polypeptide or peptide or cell expressing high levels of MCIP. The immunizing composition is administered in a manner effective to stimulate antibody producing cells. Rodents such as mice and rats are preferred animals, however, the use of rabbit, sheep frog cells is also possible. The use of rats may provide certain advantages (Goding, 1986), but mice are preferred, with the BALB/c mouse being most preferred as this is most routinely used and generally gives a higher percentage of stable fusions.

IV. Immunologic Analysis The use of antibodies of the present invention, in an ELISA assay is contemplated. For example, anti-myocardin antibodies are immobilized onto a selected surface, preferably a surface exhibiting a protein affinity such as the wells of a polystyrene microtiter plate. After washing to remove incompletely adsorbed material, it is desirable to bind or coat the assay plate wells with a non-specific protein that is known to be antigenically neutral with regard to the test antisera such as bovine serum albumin (BSA), casein or solutions of powdered milk. This allows for blocking of non-specific adsorption sites on the immobilizing surface and thus reduces the background caused by non-specific binding of antigen onto the surface.
After binding of antibody to the well, coating with a non-reactive material to reduce background, and washing to remove unbound material, the immobilizing surface is contacted with the sample to be tested in a manner conducive to immune complex (antigen/antibody) formation.
Following formation of specific immunocomplexes between the test sample and the bound antibody, and subsequent washing, the occurrence and even amount of immunocomplex formation may be determined by subjecting same to a second antibody having specificity for myocardin or a fragment thereof that differs from the first antibody. Appropriate conditions preferably include diluting the sample with diluents such as BSA, bovine gamma globulin (BGG) and phosphate buffered saline (PBS)/Tweeri . These added agents also tend to assist in the reduction of nonspecific background. The layered antisera is then allowed to incubate for from about 2 to about 4 hr, at temperatures preferably on the order of about 25° to about 27°C.
Following incubation, the antisera-contacted surface is washed so as to remove non-immunocomplexed material. A preferred washing procedure includes washing with a solution such as PBS/Tween~, or borate buffer.
To provide a detecting means, the second antibody will preferably have an associated enzyme that will generate a color development upon incubating with an appropriate chromogenic substrate. Thus, for example, one will desire to contact and incubate the second antibody-bound surface with a urease or peroxidase-conjugated anti-human IgG for a period of time and under conditions which favor the development of immunocomplex formation (e.g., incubation for 2 hr at room temperature in a PBS-containing solution such as PBS/Tween°).
After incubation with the second enzyme-tagged antibody, and subsequent to washing to remove unbound material, the amount of label is quantified by incubation with a chromogenic substrate such as urea and bromocresol purple or 2,2'-azino-di-(3-ethyl-benzthiazoline)-6-sulfonic acid (ABTS) and HZOz, in the case of peroxidase as the enzyme label. Quantitation is then achieved by measuring the degree of color generation, e.g., using a visible spectrum spectrophotometer.
The preceding format may be altered by first binding the sample to the assay plate. Then, primary antibody is incubated with the assay plate, followed by detecting of bound primary antibody using a labeled second antibody with specificity for the primary antibody.
The antibody compositions of the present invention will find great use in immunoblot or Western blot analysis. The antibodies may be used as high-affinity primary reagents for the identification of proteins immobilized onto a solid support matrix; such as nitrocellulose, nylon or combinations thereof. In conjunction with immunoprecipitation, followed by gel electrophoresis, these may be used as a single step reagent for use in detecting antigens against which secondary reagents used in the detection of the antigen cause an adverse background. Immunologically-based detection methods for use in conjunction with Western blotting include enzymatically-radiolabel-, or fluorescently-tagged secondary antibodies against the toxin moiety are considered to be of particular use in this regard.
V. Cardiomyocyte Regeneration The present invention also involves, in another embodiment, the treatment of the loss of cardiomycoytes, for example due to myocardial infarction. In particular, myocardin plays a role in cardiac myocyte development. Thus, increasing levels of myocardin in non-cardiomyocyte target cells can be used to modulate the phenotype of such target cells such that it includes one or more functions of cardiomyocytes, whereas decreasing the levels of myocardin activity in cardiomyocytes can be used to reduce or inhibit one or more cardiomyocyte functionalities and promote cell growth.

One of the therapeutic embodiments contemplated by the present inventors is the intervention, at the molecular level, in the events involved in cardiomyocyte development. Specifically, the present inventors intend to provide, to a non-cardiomyocyte target cell, for example a cardiac fibroblast cell, an expression construct capable of providing myocardin to that cell. The lengthy discussions of gene delivery means, expression vectors and the genetic elements employed therein are incorporated into this section by reference. Exemplary gene delivery vectors are viral vectors such as adenovirus, adeno-associated virus, herpesvirus, vaccinia virus, lentivirus and retrovirus, as well as lipid-based vectors.
A. Gene Therapy One skilled in the art recognizes that various methods of DNA delivery may be employed to deliver the polynucleotides of the present invention to specific cells for gene therapy. Further, in the context of gene therapy, a skilled artisan is cognizant that the vector to be utilized will generally contain the gene of interest operatively linked to a promoter. One skilled in the art also recognizes that, in certain instances, other sequences such as a 5' and/or 3'-UTR regulatory sequences are useful in expressing the gene of interest.
Where appropriate, the gene therapy vectors can be formulated into preparations in solid, semisolid, liquid or gaseous forms in the ways known in the art for their respective route of administration. Means known in the art can be utilized to prevent release and absorption of the composition until it reaches the target organ or to ensure timed release of the composition. Alternatively or additionally, the composition may be targeted by the delivery itself, for example by intracoronary delivery to target the heart (see e.g. U.S. Patents 5,792,453 and 6,100,242, hereby incorporated by reference in their entirety). A pharmaceutically acceptable form should be employed which does not deactivate the compositions of the present invention. In pharmaceutical dosage forms, the compositions can be used alone or in appropriate association, as well as in combination, with other pharmaceutically active compounds. Preferably, a sufficient amount of vector containing the therapeutice nucleic acid sequence is administered to provide a pharmacologically effective dose of the gene product, for example to alleviate symptoms associated with the disease being treated.

One skilled in the art recognizes that other methods o.f delivery may likewise be utilized to administer an expression cassette into a cell. Examples include: (1) methods utilizing physical means, such as electroporation (electricity), a gene gun (physical force) or applying large volumes of a liquid (pressure); and (2) methods wherein said expression cassette is complexed with another entity, such as a lipid-based vector (e.g., a liposome), an aggregated protein or a transporter molecule.
Certain of these embodiments are primarily suitable for ex vivo applications.
The actual dose and schedule can vary, for example, depending on whether the compositions are administered in combination with other pharmaceutical compositions, or depending on inter-individual differences in pharmacokinetics, drug disposition, and metabolism. Similarly, amounts to be administered can vary in in vitro applications, for example depending on the particular cell line utilized (e.g., based on the variable number and/or type of vector receptors present on the cell surface, or the ability of the particular vector employed for gene transfer to replicate in that cell line). Furthermore, the amount of vector to be added per cell will likely vary with the length and stability of the therapeutic gene inserted in the vector, as well as the nature of the sequence itself. Thus, vector amount is particularly a parameter which is preferably determined empirically and can be altered due to factors not inherent to the present invention (for instance, the cost associated with synthesis).
One skilled in the art can easily make adjustments to dose in accordance with the exigencies of the particular situation.
Those of skill in the art are well aware of how to apply gene delivery to in vivo situations. By way of illustration, for viral vectors, one generally will prepare a viral vector stock. Depending on the type of virus utilized and the titer attainable, one will generally deliver 1 X 104, 1 X 105, 1 X 10~, 1 X 10', 1 X 10g, 1 X 109, 1 X
101°, 1 X
1011, 1 X 1012 to 103 infectious particles to the patient. Similar figures may be extrapolated for lipid-based or other non-viral formulations by comparing relative uptake efficiencies. Formulation as a pharmaceutically acceptable composition is discussed further below. Various routes are contemplated, but local provision to the heart, preferably by the method of Hammond, et al., supra and intra-arterial or intravenous administration are preferred.

In another embodiment, it is contemplated that blocking myocardin activity may result in stimulation of the cardiomycytes to divide. This may be accomplished in one of several ways. First, one may provide an analog of myocardin's target that binds and inhibits myocardin function, effectively creating a "suicide substrate" for myocardin. This approach also could be exploited using a mimetic (see above).
Second, one could use a similar peptide target, with an additional domain actually capable of cleaving myocardin. Third, one could provide a non-functional myocardin analog that is capable of competing with myocardin peptide. And fourth, antisense or ribozyme techniques could also be used to inhibit the expression of myocardin.
B. Combined Therapy In another embodiment, it is envisioned to use myocardin in combination with other therapeutic modalities. For example, it is known that myocardin interacts with other transcription factors. Thus, the present invention further contemplates the provision of myocardin in conjunction with one or more transcription factors, and in particular, one or more cardiac transcription factors. Examples of cardiac transcription factors include, but are not limited to, GATA4, serum response factor (SRF) and Nkx2.5.
In other embodiments, in addition to the therapies described above, one may also provide to the patient more "standard" pharmaceutical cardiac therapies.
Examples of standard therapies include, without limitation, so-called "beta Mockers", anti-hypertensives, cardiotonics, anti-thrombotics, vasodilators, hormone antagonists, endothelin antagonists, calcium channel blockers, phosphodiesterase inhibitors, angiotensin type 2 antagonists and cytokine blockers/inhibitors.
Combinations may be achieved by contacting cardiac cells with a single composition or pharmacological formulation that includes both agents, or by contacting the cell with two distinct compositions or formulations, at the same time, wherein one composition includes the expression construct and the other includes the agent. Alternatively, gene therapy may precede or follow administration of the other agent by intervals ranging from minutes to weeks. In embodiments where the other agent and expression construct are applied separately to the cell, one would generally ensure that a significant period of time did not expire between the time of each delivery, such that the agent and expression construct would still be able to exert an advantageously combined effect on the cell. In such instances, it is contemplated that one would typically contact the cell with both modalities within about 12-24 hours of each other and, more preferably, within about 6-12 hours of each other, with a delay time of only about 12 hours being most preferred. In some situations, it may be desirable to extend the time period for treatment significantly, however, where several days (2, 3, 4, 5, 6 or 7) to several weeks (1, 2, 3, 4, 5, 6, 7 or 8) lapse between the respective administrations.
It also is conceivable that more than one administration of either a myocardin gene, or the other agent will be desired. In this regard, various combinations may be employed. By way of illustration, where myocardin is "A" and the other agent or cardiac transcription factor is "B," the following permutations based on 3 and 4 total administrations are exemplary:
ABlA BIAS BB/A A/AB B/A/A ABB BBB/A BBlAB
A/A/BB AB/AB ABBlA BB/A/A B/A/B/A B/A/AB BBB/A
A/A/AB B/A/A/A AB/A/A A/A/B/A ABBB B/A/BB BBlAB
Other combinations are likewise contemplated.
VII. Drug Formulations and Routes for Administration to Patients Where clinical applications are contemplated, pharmaceutical compositions will be prepared - e.g., expression vectors, virus stocks and drugs - in a form appropriate for the intended application. Generally, this will entail preparing compositions that are essentially free of pyrogens, as well as other impurities that could be harmful to humans or animals.
One will generally desire to employ appropriate salts and buffers to render delivery vectors stable and allow for uptake by target cells. Buffers also will be employed when recombinant cells are introduced into a patient. Aqueous compositions of the present invention comprise an effective amount of the vector or cells, dissolved or dispersed in a pharmaceutically acceptable carrier or aqueous medium. The phrase "pharmaceutically or pharmacologically acceptable" refer to molecular entities and compositions that do not produce adverse, allergic, or other untoward reactions when administered to an animal or a human. As used herein, "pharmaceutically acceptable carrier" includes solvents, buffers, solutions, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like acceptable for use in formulating pharmaceuticals, such as pharmaceuticals suitable for administration to humans. The use of such media and agents for pharmaceutically active substances is well know in the art. Except insofar as any conventional media or agent is incompatible with the active ingredients of the present invention, its use in therapeutic compositions is contemplated.
Supplementary active ingredients also can be incorporated into the compositions, provided they do not inactivate the vectors or cells of the compositions.
The active compositions of the present invention may include classic pharmaceutical preparations. Administration of these compositions according to the present invention may be via any common route so long as the target tissue is available via that route. This includes oral, nasal, buccal, rectal, vaginal or topical.
Alternatively, administration may be by orthotopic, intradermal, subcutaneous, intramuscular, intraperitoneal or intravenous injection. Such compositions would normally be administered as pharmaceutically acceptable compositions, as described supra.
The active compounds may also be administered parenterally or intraperitoneally. By way of illustration, solutions of the active compounds as free base or pharmacologically acceptable salts can be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils.
Under ordinary conditions of storage and use, these preparations generally contain a preservative to prevent the growth of microorganisms.
The pharmaceutical forms suitable for injectable use include, for example, sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. Generally, these preparations are sterile and fluid to the extent that easy syringability exists.
Preparations should be stable under the conditions of manufacture and storage and should be preserved against the contaminating action of microorganisms, such as bacteria and fungi.
Appropriate solvents or dispersion media may contain, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
The prevention of the action of microorganisms can be brought about by various antibacterial an antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.
Sterile injectable solutions may be prepared by incorporating the active compounds in an appropriate amount into a solvent along with any other ingredients (for example as enumerated above) as desired, followed by filtered sterilization.
Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the desired other ingredients, e.g., as enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation include vacuum-drying and freeze-drying techniques which yield a powder of the active ingredients) plus any additional desired ingredient from a previously sterile-filtered solution thereof.
For oral administration the polypeptides of the present invention generally may be incorporated with excipients and used in the form of non-ingestible mouthwashes and dentifrices. A mouthwash may be prepared incorporating the active ingredient in the required amount in an appropriate solvent, such as a sodium borate solution (Dobell's Solution). Alternatively, the active ingredient may be incorporated into an antiseptic wash containing sodium borate, glycerin and potassium bicarbonate.
The active ingredient may also be dispersed in dentifrices, including: gels, pastes, powders and slurnes. The active ingredient may be added in a therapeutically effective amount to a paste dentifrice that may include water, binders, abrasives, flavoring agents, foaming agents, and humectants.

The compositions of the present invention generally may be formulated in a neutral or salt form. Pharmaceutically-acceptable salts include, for example, acid addition salts (formed with the free amino groups of the protein) derived from inorganic acids (e.g., hydrochloric or phosphoric acids, or from organic acids (e.g., acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups of the protein can also be derived from inorganic bases (e.g., sodium, potassium, ammonium, calcium, or ferric hydroxides) or from organic bases (e.g., isopropylamine, trimethylamine, histidine, procaine and the like.
Upon formulation, solutions are preferably administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective. The formulations may easily be administered in a variety of dosage forms such as injectable solutions, drug release capsules and the like. For parenteral administration in an aqueous solution, for example, the solution generally is suitably buffered and the liquid diluent first rendered isotonic for example with sufficient saline or glucose. Such aqueous solutions may be used, for example, for intravenous, intramuscular, subcutaneous and intraperitoneal administration. Preferably, sterile aqueous media are employed as is known to those of skill in the art, particularly in light of the present disclosure. By way of illustration, a single dose may be dissolved in 1 ml of isotonic NaCI solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion, (see for example, "Remington's Pharmaceutical Sciences" 15th Edition, pages 1035-1038 and 1570-1580). Some variation in dosage will necessarily occur depending on the condition of the subject being treated. The person responsible for administration will, in any event, determine the appropriate dose for the individual subject. Moreover, for human administration, preparations should meet sterility, pyrogenicity, general safety and purity standards as required by FDA Office of Biologics standards.
VIII. Methods of Making Transgenic Mice A particular embodiment of the present invention provides transgenic animals that contain myocardin-related constructs. Transgenic. animals expressing myocardin, recombinant cell lines derived from such animals, and transgenic embryos may be useful in determining the exact role that myocardin plays in the development and differentiation of cardiomyocytes. Furthermore, this transgenic animal may provide an insight into heart development. The use o.f constitutively expressed myocardins provides a model for over- or unregulated expression. Also, transgenic animals which are "knocked out" for myocardin, in one or both alleles are contemplated.
In a general aspect, a transgenic animal is produced by the integration of a given transgene into the genome in a manner that permits the expression of the transgene. Methods for producing transgenic animals are generally described by Wagner and Hoppe (U.S. Patent 4,873,191; which is incorporated herein by reference), Brinster et al., 1985; which is incorporated herein by reference in its entirety) and in Hogan et al. (1994).
Typically, a gene flanked by genomic sequences is transferred by microinjection into a fertilized egg. The microinjected eggs are implanted into a host female, and the progeny are screened for the expression of the transgene.
Transgenic animals may be produced from the fertilized eggs from a number of animals including, but not limited to reptiles, amphibians, birds, mammals, and fish.
DNA clones for microinjection can be prepared by any means known in the art. For example, DNA clones for microinjection can be cleaved with enzymes appropriate for removing the bacterial plasmid sequences, and the DNA
fragments electrophoresed on 1 % agarose gels in TBE buffer, using standard techniques.
The DNA bands are visualized by staining with ethidium bromide, and the band containing the expression sequences is excised. The excised band is then placed in dialysis bags containing 0.3 M sodium acetate, pH 7Ø DNA is electroeluted into the dialysis bags, extracted with a 1:l phenol:chloroform solution and precipitated by two volumes of ethanol. The DNA is redissolved in 1 ml of low salt buffer (0.2 M NaCI, 20 mM
Tris,pH 7.4, and 1 mM EDTA) and purified on an Elutip-DTM column. The column is first primed with 3 ml of high salt buffer (1 M NaCI, 20 mM Tris, pH 7.4, and 1 mM
EDTA) followed by washing with 5 ml of low salt buffer. The DNA solutions are passed through the column three times to bind DNA to the column matrix. After one wash with 3 ml of low salt buffer, the DNA is eluted with 0.4 ml high salt buffer and precipitated by two volumes of ethanol. DNA concentrations are measured by absorption at 260 nm in a UV spectrophotometer. For microinjection, DNA
concentrations are adjusted to 3 p,g/ml in 5 mM Tris, pH 7.4 and 0.1 mM EDTA.

Other methods for purification of DNA for microinjection are described in Hogan et al. (1986), in Palmiter et al. (1982); and in Sambrook et al. (1989).
In an exemplary microinjection procedure, female mice six weeks of age are induced to superovulate with a S IU injection (0.1 cc, ip) of pregnant mare serum gonadotropin (PMSG; Sigma) followed 48 hours later by a 5 ILT injection (0.1 cc, ip) of human chorionic gonadotropin (hCG; Sigma). Females are placed with males immediately after hCG injection. Twenty-one hours after hCG injection, the mated females are sacrificed by COZ asphyxiation or cervical dislocation and embryos are recovered from excised oviducts and placed in Dulbecco's phosphate buffered saline with 0.5% bovine serum albumin (BSA; Sigma). Surrounding cumulus cells are removed with hyaluronidase (1 mg/ml). Pronuclear embryos are then washed and placed in Earle's balanced salt solution containing 0.5 % BSA (EBSS) in a 37.5°C
incubator with a humidified atmosphere at 5% C02, 95% air until the time of injection. Embryos can be implanted at the two-cell stage.
Randomly cycling adult female mice are paired with vasectomized males.
C57BL/6 or Swiss mice or other comparable strains can be used for this purpose.
Recipient females are mated at the same time as donor females. At the time of embryo transfer, the recipient females are anesthetized with an intraperitoneal injection of 0.015 ml of 2.5 % avertin per gram of body weight. The oviducts are exposed by a single midline dorsal incision. An incision is then made through the body wall directly over the oviduct. The ovarian bursa is then torn with watchmakers forceps. Embryos to be transferred are placed in DPBS (Dulbecco's phosphate buffered saline) and in the tip of a transfer pipet (about 10 to 12 embryos).
The pipet tip is inserted into the infundibulum and the embryos transferred. After the transfer, the incision is closed by two sutures.

IX. Screening Assays The present invention also contemplates the screening of compounds for various abilities to interact with and/or affect myocardin expression or function.
Particularly preferred compounds will be those useful in inhibiting or promoting the actions of myocardin in regulating the development and differentiation of cardiomyocytes. In the screening assays of the present invention, the candidate substance may first be screened for basic biochemical activity -- e.g., binding to a target molecule -- and then tested for its ability to inhibit modulate activity, at the cellular, tissue or whole animal level.
A. Modulators and Assay Formats i) Assay Formats The present invention provides methods of screening for modulators of myocardin expression and binding to other proteins or nucleic acids. In one embodiment, the present invention is directed to a method of:
(a) providing a myocardin polypeptide;
(b) contacting the myocai-din polypeptide with the candidate substance;
and (c) determining the binding of the candidate substance to myocardin polypeptide.
In yet another embodiment, the assay looks not at binding, but at myocardin function. Such methods would comprise, for example:
(a) providing myocardin and DATA to a cell;
(b) admixing myocardin and GATA in the presence of a candidate modulator; and (c) measuring the effect of the candidate substance on the expression of a cardiac cell gene product.

A related assay that examines the interaction of myocardin and GATA would comprise:
(a) providing myocardin and GATA to a cell;
(b) admixing myocardin and GATA in the presence of a candidate substance; and (c) measuring the effect of the candidate substance on the interaction of myocardin and GATA.
Both of the preceding assays could be performed substituting SRF or Nkx2.5 for GATA.
In still yet other embodiments, one would look at the effect of a candidate substance on the expression of myocardin. This can be done by examining mRNA
expression, although alterations in mRNA stability and translation would not be accounted for. A more direct way of assessing expression is by directly examining protein levels, for example, through Western blot or ELISA.
ii) Inhibitors and Activators An inhibitor according to the present invention may be one which exerts an inhibitory effect on the expression or function of myocardin. By the same token, an activator according to the present invention may be one which exerts a stimulatory effect on the expression or function of myocardin.

iii) Candidate Substances As used herein, the term "candidate substance" refers to any molecule that may potentially modulate myocardin expression or function. The candidate substance may be a protein or fragment thereof, a small molecule inhibitor, or even a nucleic acid molecule. It may prove to be the case that the most useful pharmacological compounds will be compounds that are structurally related to compounds which interact naturally with myocardin. Creating and examining the action of such molecules is known as "rational drug design," and include making predictions relating to the structure of target molecules.
The goal of rational drug design is to produce structural analogs of biologically active polypeptides or target compounds. By creating such analogs, it is possible to fashion drugs which are more active or stable than the natural molecules, which have different susceptibility to alteration or which may affect the function of various other molecules. In one approach, one would generate a three-dimensional structure for a molecule like myocardin, and then design a molecule for its ability to interact with myocardin. Alternatively, one could design a partially functional fragment of myocardin (binding, but no activity), thereby creating a competitive inhibitor. This could be accomplished by x-ray crystallography, computer modeling or by a combination of both approaches.
It also is possible to use antibodies to ascertain the structure of a target compound or inhibitor. In principle, this approach yields a pharmacore upon which subsequent drug design can be based. It is possible to bypass protein crystallography altogether by generating anti-idiotypic antibodies to a functional, pharmacologically active antibody. As a mirror image of a mirror image, the binding site of anti-idiotype would be expected to be an analog of the original antigen. The anti-idiotype could then be used to identify and isolate peptides from banks of chemically- or biologically-produced peptides. Selected peptides would then serve as the pharmacore. Anti-idiotypes may be generated using the methods described herein for producing antibodies, using an antibody as the antigen.
On the other hand, one may simply acquire, from various commercial sources, small molecule libraries that are believed to meet the basic criteria for useful drugs in an effort to "brute force" the identification of useful compounds. Screening of such libraries, including combinatorially generated libraries (e.g., peptide libraries), is a rapid and efficient way to screen large number of related (and unrelated) compounds for activity. Combinatorial approaches also lend themselves to rapid evolution of potential drugs by the creation of second, third and fourth generation compounds modeled of active, but otherwise undesirable compounds.
Candidate compounds may include fragments or parts of naturally-occurring compounds or may be found as active combinations of known compounds which are otherwise inactive. It is proposed that compounds isolated from natural sources, such as animals, bacteria, fungi, plant sources, including leaves and bark, and marine samples may be assayed as candidates for the presence of potentially useful pharmaceutical agents. It will be understood that the pharmaceutical agents to be screened could also be derived or synthesized from chemical compositions or man-made compounds. Thus, it is understood that the candidate substance identified by the present invention may be polypeptide, polynucleotide, small molecule inhibitors or any other compounds that may be designed through rational drug design starting from known inhibitors of hypertrophic response.
Other suitable inhibitors include antisense molecules, ribozymes, and antibodies (including single chain antibodies).
It will, of course, be understood that the screening methods of the present invention are useful in themselves notwithstanding the fact that effective candidates may not be found. The invention provides methods for screening for such candidates, not solely methods of finding them.
B. In Vitro Assays A quick, inexpensive and easy assay to run is a binding assay. Binding of a molecule to a target may, in and of itself, be inhibitory, due to steric, allosteric or charge-charge interactions. This can be performed in solution or on a solid phase and can be utilized as a first round screen to rapidly eliminate certain compounds before moving into more sophisticated screening assays. In one embodiment of this kind, the screening of compounds that bind to a myocardin molecule or fragment thereof is provided The target may be either free in solution, fixed to a support, expressed in or on the surface of a cell. Either the target or the. compound may be labeled, thereby permitting determining of binding. In another embodiment, the assay may measure the inhibition of binding of a target to a natural or artificial substrate or binding partner (such as myocardin). Competitive binding assays can be performed in which one of the agents (myocardin for example) is labeled. Usually, the target will be the labeled species, decreasing the chance that the labeling will interfere with the binding moiety's function. One may measure the amount of free label versus bound label to determine binding or inhibition of binding.
A technique for high throughput screening of compounds is described in WO
84/03564. Large numbers of small peptide test compounds are synthesized on a solid substrate, such as plastic pins or some other surface. The peptide test compounds are reacted with, for example, myocardin and washed. Bound pelypeptide is detected by various methods.
Purified target, such as myocardin, can be coated directly onto plates for use in the aforementioned drug screening techniques. However, non-neutralizing antibodies to the polypeptide can be used to immobilize the polypeptide to a solid phase.
Also, fusion proteins containing a reactive region (preferably a terminal region) may be used to link an active region (e.g., the C-terminus of myocardin) to a solid phase.
C. In Cyto Assays Various cell lines that express myocardin can be utilized for screening of candidate substances. For example, cells containing myocardin with an engineered indicators can be used to study various functional attributes of candidate compounds.
In such assays, the compound would be formulated appropriately, given its biochemical nature, and contacted with a target cell.
Depending on the assay, culture may be required. As discussed above, the cell may then be examined by virtue of a number of different physiologic assays (growth, size, Ca++ effects). Alternatively, molecular analysis may be performed in which the function of myocardin and related pathways may be explored. This involves assays such as those for protein expression, enzyme function, substrate utilization, mRNA
expression (including differential display of whole cell or polyA RNA) and others.
D. In Yivo Assays The present invention particularly contemplates the use of various animal models. Transgenic animals may be created with constructs that permit myocardin expression and activity to be controlled and monitored. The generation of these animals has been described elsewhere in this document.
Treatment of these animals with test compounds will involve the administration of the compound, in an appropriate form, to the animal.
Administration will be by any route the could be utilized for clinical or non-clinical purposes, including but not limited to oral, nasal, buccal, or even topical.
Alternatively, administration may be by intratracheal instillation, bronchial instillation, intradermal, subcutaneous, intramuscular, intraperitoneal or intravenous injection. Specifically contemplated are systemic intravenous injection, regional administration via blood or lymph supply.
E. Production of Inhibitors In an extension of any of the previously described screening assays, the present invention also provide for methods of producing inhibitors. The methods comprising any of the preceding screening steps followed by an additional step of "producing the candidate substance identified as a modulator of ' the screened activity.
X. Examples The following examples are included to further illustrate various aspects of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques and/or compositions discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

Expression Pattern of Myocardin 1 During Early Heart Development The heart is the first organ to form during mammalian development. Cardiac muscle cells originate from a region of the embryo known as the cardiac crescent and develop into a primitive heart tube along the midline of the embryo (FIG. 1).
Because this is the only region of the embryo that can give rise to cardiac muscle cells, it would be expected to express a unique set of genes responsible for cardiogenesis. By identifying the genes that are uniquely expressed in this region, master control genes for heart formation can be identified. Subsequent embryonic events of looping, chamber maturation and alignment with the vascular system give rise to the mature four-chambered heart (Olson et al., 1996 and Fishman et al., 1997).
Expression of myocardin 1 was determined by whole-mount (FIG. 3A) or section (FIG. 3B and FIG. 3C) in situ hybridizations to mouse embryos at E7.75 (FIG.
3A), E8.0 (FIG. 3B), and E12.5 (FIG. 3C).
In situ hybridization to cellular RNA was performed using standard techniques well known in the art, e.g., fluorescence in situ hybridization (FISH).
Briefly, the samples were fixed for the appropriate time and dehydrated through a graded ethanol series. The samples were then impregnated in paraffin wax and cast into blocks. The samples were sectioned on a microtome. A specific labeled probe was prepared.
The probe can be labeled with biotin or digoxigenin or with a fluorochrome-tagged deoxynucleotide. Next, the probe was hybrized to the sample. Hybridization conditions may vary with the different labeled probes. After the hybridization, samples were washed for 15 min in 37°C 50% formamide/2 x SSC, 15 min in 37°C 2 x SSC and 15 min in room temperature 1 x SSC. The slides were equilibrated for min in 4 x SSC at room temperature. The slides were drained and allowed to air dray.
Next, a detection solution was added. After a 45 min incubation in the detection solution, the slides were washed. A counterstain of DAPI or propidium iodide staining solution was added to the slide. The slide was viewed using a fluorescence microscope.

The results in FIG. 3 illustrate the expression pattern of myocardin 1 during early heart development. In FIG. 3A, myocardin 1 transcripts can be seen localized to the cardiac crescent. In FIG. 3B, transcripts are present throughout the heart tube in a transverse section. In FIG. 3C, transcripts are seen throughout the developing heart in a sagittal section.
As might be expected given its role in embryonic development, myocardin has also been shown to be expressed in a subset of embryonic vascular and visceral smooth muscle cells. At E13.5, myocardin expression was evident within smooth muscle cells lining the walls of the esophagus and aortic arch arteries, as well as the pulmonary outflow tract. Expression in these smooth muscle cell types was still apparent, but was diminished, by E15.5. Myocardin expression was also detected in smooth muscle cells within the lung and gut, as well as in head mesenchyme, which may serve as a source of smooth muscle precursors. Myocardin was not expressed at detectable levels in skeletal muscle.

Expression Pattern of Myocardin 1 in Adult 'Mouse Tissues The expression of myocardin 1 transcripts in adult mouse tissues was analyzed by Northern blot, utilizing techniques well known in the art. RNA was isolated from adult mouse heart, brain, spleen, lung, liver, skeletal muscle, kidney and testis according to standard RNA isolation procedures, e.g., phenol/chloroform/isoamyl alcohol (RNAzoI, Life Technologies, Inc.) or guanidine thiocyanate.
Briefly, fractionated RNA was transferred from an agarose gel to a membrane by upward capillary action. The transferred RNA is cross-linked to the membrane.
Next, a radiolabeled probe (DNA or RNA) was hybridized to the membrane in a formamide solution. After hybridization, autoradiography was performed to detect the transcripts.
The results in FIG. 4 show that the transcripts were detected only in the heart.
A RNA molecular marker illustrates the size of the transcripts.

Nuclear Localization of Myocardin 1 Protein Cos cells were transiently transfected with an expression vector encoding myocardin 1 with a Flag-epitope tag. Transient transfection assays were performed using standard methods, such as LifofectAMINE plus (Life Technologies, Inc.), calcium phosphate or electroporation. Briefly, the cells were plated 12 hr before transfection in tissue culture dishes. They were transfected with a total of about 0.5-1.0 ~g of plasmid DNA. The subcellular location of myocardin 1 protein was determined by immunostaining with anti-Flag antibody.
All myocardin 1 protein is localized to the nucleus as illustrated in FIG. 5.
The inset in the lower right corner shows an enlargement of a single cell, with strong myocardin 1 staining in the nucleus, but excluded from the nucleoli.

Structure of Myocardin 1 and Mapping of Transcription Activation Domains Portions of myocardin 1 were fused to the DNA binding domain of yeast GAL4 and tested in transfected Cos cells for transcriptional activity against a GAL4-dependent luciferase reporter. The relative transcriptional activities of different myocardin 1 fragments are show in FIG. 6.
The nuclear localization sequence (NLS) is located between residues 245 and 254, within a basic region at residues 243-260. A glutamine-rich (Q) domain is located between residues 287-320. The SAP domain is found at residues 380-414.
The transcription activation domain is located at the carboxyl-terminus at 670 to 935.
The carboxyl-terminus is an extremely potent transcription activation domain, able to activate the reporter over 1000-fold, to a level comparable to that of the powerful viral coactivator VP16 (not shown).
As might be expected, given its apparent influence on transcription, myocardin contains an SAP domain (named for nuclear scaffold attachment factors A and B), as found in a variety of proteins that affect not only transcription but also nuclear architecture. The SAP domain is a 35 amino acid motif containing two predicted amphipathic helices separated by an intervening region with an invariant glycine residue. Functional aspects of the SAP domain were examined by introducing proline mutations into helix-1 or -2. These mutations had only a modest effect on the ability of myocardin to transactivate the SM22 promoter (which transactivtation is discussed further below). Similarly, the deletion of the linker region between the two helices of the SAP domain, shown previously to be required for DNA binding by SAF-A, had little effect on SM22 activation, but eliminated ANF activation (discussed below).

Traps-Activation of the SM22 Promoter by Myocardin Cos cells were transiently transfected with a luciferase reporter gene containing the 1.4 kb SM22 promoter and expression vectors encoding myocardin and SRF. Briefly, the cells were, plated 12 hr before transfection in tissue culture dishes. They were transfected with plasmid DNA. Forty eight hr after transfection, the cells were harvested. Luciferase assays of whole cell extracts were conducted by standard methods well known in the art.
FIG. 7A shows activity of the wild-type SM22 promoter, which was transactivated about 100-fold by myocardin. FIG. 7B shows activity of the SM22 promoter with a mutation in the distal CArG box (CArG-far). This promoter was also activated by myocardin, but not to the same extent as the wild-type promoter.
FIG.
7C shows activity of the SM22 promoter with a mutation in the proximal CArG
box (CArG-near). This promoter has lost almost all responsiveness to myocardin, as has the promoter with both the CArG boxes mutated, (FIG. 7D). Both myocardin 1 and N-terminally truncated myocardin 1 have demonstrated similar activities in these assays.
Additional studies have further demonstrated myocardin's potency as a transactivator and its preferential action via CArG boxes. By way of example, myocardin's ability to transactivate reporter genes containing four tandem copies of SM22 CArG-near or the c fos SRE linked to the E 1 b promoter was tested and compared to SRF. These reporters were transactivated several hundred-fold by myocardin, whereas SRF was only able to activate expression by 8-fold.

Myocardin 1 and MEF2C Cooperatively Activate the MLC2V Promoter Cos cells were transiently transfected with a luciferase reporter gene containing the MLC2V promoter and expression vectors encoding myocardin 1 and MEF2C, as indicated. Forty eight hr later, cells were harvested and luciferase activity was assayed. The results in FIG. 8 show that myocardin 1 and MEF2C
synergistically activate MLC2V transcription. Both myocardin 1 and N-terminally truncated myocardin 1 have demonstrated similar activities in these assays.

Interactions of Myocardin 1 and GATA4 A. GATA4 Represses Myocardin Activation of the ANF Promoter HeLa cells and Cos cells were transiently transfected with a luciferase reporter gene containing the ANF promoter and expression vectors encoding myocardin 1 and GAT A4, as indicated. Forty eight hr later, cells were harvested and luciferase activity was assayed. The results in FIG. 9 show that GATA4 represses myocardin 1 activation of ANF transcription.
B. Myocardin 1 and GATA4 Cooperatively Activate the Nkx2.5 Promoter HeLa cells (and/or Cos cells) were transiently transfected with a luciferase reporter gene containing the Nkx2.5 promoter and expression vectors encoding myocardin 1 and GATA4. Approximately forty eight hr later, cells were harvested and luciferase activity was assayed. The results demonstrated that myocardin 1 and GATA4 cooperatively activated Nkx2.5 transcription. Both myocardin 1 and N-ternlinally truncated myocardin 1 have demonstrated similar activities in these GATA4 interaction assays. FIG.13.

Myocardin 1 and Nkx2.5 Cooperatively Activate the a-MHC Promoter HeLa cells were transiently transfected with a luciferase reporter gene containing the a-MHC promoter and expression vectors encoding myocardin 1 and Nkx2.5. Forty eight hr later; cells were harvested and luciferase activity was assayed.
The results in FIG. 10 show that myocardin 1 and Nkx2.5 synergistically activate a-MHC transcription. EXAMPLE 9Myocardin Forms a Complex with SRFTo further examine the mechanism for CArG box-dependent transcriptional activation, the inventors tested whether myocardin translated in vitro could bind to the CArG
boxes from the SM22 promoter. S1RF' bound to both CArG boxes, but no binding of myocardin to either CArG box was detectable in gel mobility shift assays.
However, myocardin in the presence of SRF gave rise to a prominent ternary complex with the CArG box sequence. This ternary complex was supershifted by antibodies against SRF or FLAG-tagged myocardin. The total amount of SRF DNA binding was comparable in the presence and absence of myocardin, suggesting that association of SIRf with myocardin does not alter the affinity of SRF fro the CArG box.
Myocardin and SRF also formed a ternary complex with the c fos and ANF CArG boxes, the intensity of which correlated directly with the relative binding of SRF, to the site. The lack of obvious homology in the flanking sequences of these different CArG
boxes suggests that myocardin associates directly with SRF and does not depend on specific DNA sequences for ternary complex formation.
The region of myocardin required for ternary complex formation with SRF
was determined using myocardin deletion mutants. Deletion of the amino-terminal 276 amino acid abolished association with SRF, as did larger amino-terminal deletions. In contrast, deletions from near the middle of the protein to the carboxyl terminus did not affect SRF interaction. Deletion of the Q-rich domain or the basic regions also abolished ternary complex formation, whereas mutation of the SAP
domain did not. These findings are consistent with the interpretation that the amino terminus of myocardin confers transcriptional specificity by mediating association with SRF, whereas the carboxyl terminus activates transcription.

To determine whether myocardin interacts with the DNA binding or transcription activation domain of SRF, the inventors performed gel mobility shift assays with an SRF deletion mutant encompassing the MADS domain, but lacking the amino and carboxyl termini. This SRF mutation (SRF 100-300) bound the CArG box sequence and formed a ternary complex with myocardin.
Association of myocardin and SRF was also readily detectable in coimmunoprecipitation assays of epitope-tagged proteins. Interaction was dependent on the amino-terminal regions of myocardin.. The core MADS domain of SRF
(residues 133-266) was also necessary and sufficient to mediate association with myocardin in coimmunoprecipitation assays.
Without wishing to be bound by any particular theory, these results suggest that myocardin interacts with SRF to form a stable ternary complex which may be an aspect of the mechanism of action of myocardin as a transcription activator.
Both myocardin 1 and N-terminally truncated myocardin 1 have demonstrated similar activities in this regard.
iVlyocardin has also been shown to be sensitive to the level of SRF, such that at low concentrations of SRF expression plasmid; myocardin and SRF
synergistically activated SM22 transcription, whereas at higher concentrations of SRF, transcriptional activation by myocardin was reduced. Inhibition of myocardin-dependent transcription by excess SRF could be relieved by increasing the amount of myocardin.
Thus, the ratio of SRF to myocardin appears relevant for transcriptional activation by myocardin, such that exceeding an optimal ratio with an excess of SRF can result in attenuation of myocardin activity.

Inhibition of Cardiomyocyte Differentiation in Xenopus Embryos by Dominant Negative Myocardin Further confirming the role of myocardin in cardiomyocyte differentiation, mRNA from a dominant negative myocardin mutant was injected into Xenopus embryos. A dramatic reduction in the expression of transcripts for cardiac a-actin and a-tropomyosin was observed. The effects on cardiac differentiation were highly specific as demonstrated by the normal overall appearance of the embryo. Also observed was a dose-dependent reduction in expression of cardiac markers, such that approximately 90% of injected embryos exhibited a reduction or complete elimination of cardiac gene expression.

Overexpression of Myocardin Induces Hypertrophy in Cardiomyocytes The inventors have investigated how myocardin affects the growth and/or differentiation of cardiomyocytes by overexpressing myocardin in cardiomyocytes using adenoviral delivering system. Cardiomyocyte cultures were prepared by dissociation of 1-day-old neonatal rat hearts and were plated differentially to remove fibroblasts. Cells were plated on glass coverslips coated with 4 pg/cm2 laminin in 4:1 Dulbecco's modified Eagle's medium (DMEM):199 medium with 10% horse serum and 5% fetal calf serum at a density of 5 x 104 cells/cmZ. Eighteen hours after plating, cells were changed into serum-free media and infected with adenoviruses expressing either myocardin or 13-galactosidase (as a control) at a multiplicity of infection (m.o.i.) of 100.
For immunofluorescence, cells were fixed in 3.7% formaldehyde on ice for 30 min, permeabilized with 0.1% Triton X-100 in phosphate-buffered saline (PBS) and blocked with 5% serum in PBS for 1 hour at room temperature. Cells were incubated with monoclonal anti-a-actinin (sarcomeric) or anti-ANF (atrial natriuretic factor) antibodies at a dilution of 1:200 in blocking buffer for 1 hour at 37°C, washed and incubated with fluorescein-conjugated horse anti-mouse IgG antibody at a dilution of 1:200 in blocking buffer for 1 hour at 37°C. Following secondary antibody incubation, cells were washed with PBS.
The results are shown in FIGS. 11 and 12. Overexpression of myocardin in neonatal cardiomyocytes induces assembly of sacomeres and expression of atrium natriuretic factor (ANF), markers of cardiac hypertrophy.

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SEQUENCE LISTING
<110> OLSON, ERIC N.
WANG, DA-ZHI
<120> METHODS AND COMPOSITIONS RELATING TO A CARDIAC-SPECIFIC
NUCLEAR REGULATORY FACTOR
<130> UTSD:695US
<140> UNKNOWN
<141> 2001-12-20 <150> 60/257,761 <151> 2000-12-21 <160> 30 <170> PatentIn Ver. 2.1 <210> 1 <211> 4959 <212> DNA
<213> Mus musculus <220>
<221> CDS
<222> (641)..(3061) <400> 1 ggaattcggc acgaggccac cctcagagga ggagggtcct gcctgctggg agttaattag 60 cctcgcgagc ggcgaggggg gaggcgccag ttttctgggg acactggcgg ccactgtgcg 120 tcctcctacc caagggagct ccccaagagt tggatgaatt ctgggttgtt agctgctgtc 180 ctctgggctc ccgggagcca gtttctggtg gaaagcgggg cgcctggcca acgaccagcg 240 gcttgctgag actcaccatg acactcctgg ggtctgaaca ctctttgctg attagaagga 300 agttccgatc agtcttacag ttacggcttc aacagagaag gacccaggag cagctggcta 360 accaaggctt aataccgcca ctgaaaggtc caactgaatt ccatgacccg agaaaacaat 420 tggatagtgc caagactgaa gattccctga ggcgcaaggg cagaaacagg tccgaccgtg 480 ccagcctggt tactatgcac attct~ccaag cctccacggc agaaaggtcc attccaactg 540 ctcagatgaa gctcaaaaga gcccgccttg cagatgacct caatgagaag atcgctctcc 600 gccaaggccc ttggaactgg tggagaagaa cattctgccg atg gat tct tcc gtg 655 Met Asp Ser Ser Val aaa gag get ata aaa ggt act gag gtg agc ctc tcc aag gca gca gat 703 Lys Glu Ala Ile Lys Gly Thr Glu Val Ser Leu Ser Lys Ala Ala Asp gca ttc gcc ttt gag gat gac agc agt aga gat ggg ctc tct cca gat 751 Ala Phe Ala Phe Glu Asp Asp Ser Ser Arg Asp Gly Leu Ser Pro Asp cag get agg agc gag gac ccc cag ggc tct aca gga tcc acc cca gac 799 Gln Ala Arg Ser Glu Asp Pro Gln Gly Ser Thr Gly Ser Thr Pro Asp atc aaa tcc act gag get cct ctg gac aca atc cag gat ctc act cct 847 Ile Lys Ser Thr Glu Ala Pro Leu Asp Thr Ile Gln Asp Leu Thr Pro ggc tca gaa agt gac aag aat gat gca gcc tcc cag cca ggc aac cag 895 Gly Ser Glu Ser Asp Lys Asn Asp Ala Ala Ser Gln Pro Gly Asn Gln tca gac cct ggg aag cag gtt ctc ggc ccc ctc agc acc ccg att cct 943 Ser Asp Pro Gly Lys Gln Val Leu Gly Pro Leu Ser Thr Pro Ile Pro gtg cac act get gta aag tcc aag tct ttg ggt gac agt aag aac cgc 991 Val His Thr Ala Val Lys Ser Lys Ser Leu Gly Asp Ser Lys Asn Arg cac aaa aag ccc aaa gac ccc aaa cca aag gtg aag aag ctc aaa tac 1039 His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val Lys Lys Leu Lys Tyr cat cag tac atc ccc cca gac cag aag gca gag aag tct ccc cca ccc 1087 His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu Lys Ser Pro Pro Pro atg gac tct gcc tat gcc cgg ctg ctc cag caa cag cag cta ttc ctg 1135 Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln Gln Gln Leu Phe Leu cag cta cag atc ctc agc cag cag cag caa cag cag cag caa cag cag 1183 Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln cag cag caa cag cag cag cag cag cag cag cag cgg ttc agc tac cct 1231 Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Arg Phe Ser Tyr Pro ggg atg cac caa aca cac ctc aaa gaa cca aat gaa cag atg gcc aga 1279 Gly Met His Gln Thr His Leu Lys Glu Pro Asn Glu Gln Met Ala Arg aat ccg aat cct tct tca aca cca ctg agc aat acc cct cta tcc cct 1327 Asn Pro Asn Pro Ser Ser Thr Pro Leu Ser Asn Thr Pro Leu Ser Pro gtc aaa aat agc att tct gga caa act ggt gtt tct tct ctc aaa cca 1375 Val Lys Asn Ser Ile Ser Gly Gln Thr Gly Val Ser Ser Leu Lys Pro ggc ccc ctc cca ccc aac ctg gat gat ctc aag gtg tca gag tta aga 1423 Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys Val Ser Glu Leu Arg caa cag ctt cga atc cgg ggc ttg cca gtg tca ggc acc aag aca gcg 1471 Gln Gln Leu Arg Ile Arg Gly Leu Pro Val Ser Gly Thr Lys Thr Ala ctg gtg gac cgg ctt cgt ccc ttc cag gat tgt get ggc aac cct gtg 1519 Leu Val Asp Arg Leu Arg Pro Phe Gln Asp Cys Ala Gly Asn Pro Val ccc aac ttt ggg gac atc aca act gtc acc ttt cct gtc acg ccc aac 1567 Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe Pro Val Thr Pro Asn acc ttg ccc agt tat cag tcc tcc ccg aca ggc ttc tac cac ttt ggc 1615 Thr Leu Pro Ser Tyr Gln Ser Ser Pro Thr Gly Phe Tyr His Phe Gly agc aca agc tcc agc cca ccc atc tcc ccc gcc tca tct gac ttg tcc 1663 Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala Ser Ser Asp Leu Ser get gca ggg tcc ctg cca gac acc ttc acc gat gcg tca cct ggc ttc 1711 Ala Ala Gly Ser Leu Pro Asp Thr Phe Thr Asp Ala Ser Pro Gly Phe ggc ctg cac gca tct ccg gtg ccc gcc tgc acg gac gag agt ctg ctg 1759 Gly Leu His Ala Ser Pro Val Pro Ala Cys Thr Asp Glu Ser Leu Leu agc agc ctg aat ggg ggc tcg ggc ccc tcc gag cct gat ggg cta gac 1807 Ser Ser Leu Asn Gly Gly Ser Gly Pro Ser Glu Pro Asp Gly Leu Asp tct gag aag gac aag atg ctg gtg gag aag cag aaa gtg atc aac cag 1855 Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln Lys Val Ile Asn Gln ctc acc tgg aag ctg cgg caa gag cag cgg cag gtg gaa gag ctg aga 1903 Leu Thr Trp Lys Leu Arg Gln Glu Gln Arg Gln Val Glu Glu Leu Arg atg caa ctg cag aag cag aag agc agc tgc agc gac cag aag cca ctg 1951 Met Gln Leu Gln Lys Gln Lys Ser Ser Cys Ser Asp Gln Lys Pro Leu ccc ttc ttg gcc acc acc atc aaa cag gaa gat gtc tcc agc tgc ccc 1999 Pro Phe Leu Ala Thr Thr Ile Lys Gln Glu Asp Val Ser Ser Cys Pro ttc gca ccc cag cag gcg tct ggg aag gga cag ggc cac agc tct gac 2047 Phe Ala Pro Gln Gln Ala Ser Gly Lys Gly Gln Gly His Ser Ser Asp agt ccc cct ccg get tgt gag acg get cag ctg ctg cct cac tgt gtg 2095 Ser Pro Pro Pro Ala Cys Glu Thr Ala Gln Leu Leu Pro His Cys Val gag tcc tca ggt caa acc cat gta ctc tcg tcc acg ttt ctc agc ccc 2143 Glu Ser Ser Gly Gln Thr His Val Leu Ser Ser Thr Phe Leu Ser Pro cag tgc tcc cct cag cac tcg ccc ctg ggg ggc ctg aag agc ccg cag 2191 Gln Cys Ser Pro Gln His Ser Pro Leu Gly Gly Leu Lys Ser Pro Gln cac atc agc ctg cct cca tca ccc aac aac cat tac ttc ctg get tcc 2239 His Ile Ser Leu Pro Pro Ser Pro Asn Asn His Tyr Phe Leu Ala Ser tct tcg gga get cag aga gag aac cat ggg gtc tct tca ccc agc agc 2287 Ser Ser Gly Ala Gln Arg Glu Asn His Gly Val Ser Ser Pro Ser Ser agc caa ggg tgc gca cag atg act ggt tta caa tct tct gac aag gtg 2335 Ser Gln Gly Cys Ala Gln Met Thr Gly Leu Gln Ser Ser Asp Lys Val ggg cca acg ttt tca att cca tcc cca act ttt tct aag tca agt tca 2383 Gly Pro Thr Phe Ser Ile Pro Ser Pro Thr Phe Ser Lys Ser Ser Ser gca gtt tca gat atc acc cag ccc cca tcc tat gaa gat gca gtg aag 2431 Ala Val Ser Asp Ile Thr Gln Pro Pro Ser Tyr Glu Asp Ala Val Lys cag caa atg act cgg agt cag cag atg gac gaa ctc ctg gat gtc ctc 2479 Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu Leu Leu Asp Val Leu att gaa agt gga gaa atg cca gcc gat gcc agg gaa gat cat tca tgt 2527 Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg Glu Asp His Ser Cys ctt cag aaa att cca aag atc cct ggg tcc tcc tgc agc cca act gcc 2575 Leu Gln Lys Ile Pro Lys Ile Pro Gly Ser Ser Cys Ser Pro Thr Ala atc ccc ccg aag ccc tcg get tcc ttt gag cag gca tct tcg gga ggc 2623 Ile Pro Pro Lys Pro Ser Ala Ser Phe Glu Gln Ala Ser Ser Gly Gly cag atg gcc ttc gat cac tac gcc aac gac agt gac gaa cac ctg gaa 2671 Gln Met Ala Phe Asp His Tyr Ala Asn Asp Ser Asp Glu His Leu Glu gtc tta ttg aat tct cac agc ccc atc gga aag gtg agc gat gtt acc 2719 Val Leu Leu Asn Ser His Ser Pro Ile Gly Lys Val Ser Asp Val Thr ctc ctc aaa atc gga agc gag gag cct cct ttt gac agc atc atg gat 2767 Leu Leu Lys Ile Gly Ser Glu Glu Pro Pro Phe Asp Ser Ile Met Asp ggc ttc cca ggg aag get gcg gaa gat ctc ttc agt get cac gag ctc 2815 Gly Phe Pro Gly Lys Ala Ala Glu Asp Leu Phe Ser Ala His Glu Leu ttg cct ggg ccc ctc tcc ccg atg cat gca cag ttg tca cct cct tct 2863 Leu Pro Gly Pro Leu Ser Pro Met His Ala Gln Leu Ser Pro Pro Ser gtg gac agc agt ggt ctg cag ctg agc ttc acg gaa tct cct tgg gaa 2911 Val Asp Ser Ser Gly Leu Gln Leu Ser Phe Thr Glu Ser Pro Trp Glu aca atg gaa tgg ctg gac ctc act cca cct agt tcc acg cca ggc ttc 2959 Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Ser Ser Thr Pro Gly Phe agc aac ctt acc tcc agt ggg ccc agc att ttc aac atc gat ttt ctg 3007 Ser Asn Leu Thr Ser Ser Gly Pro Ser Ile Phe Asn Ile Asp Phe Leu gat gtt aca gat ctt aat ctg aat tcc cct atg gat ctc cac tta cag 3055 Asp Val Thr Asp Leu Asn Leu Asn Ser Pro Met Asp Leu His Leu Gln cag tgg taaacacccg aggtacaaga gctacgagag ctcagtggga attcaatgga 3111 Gln Trp ggaaagcacg ataccggaaa tgtgtgttcc aaaagatgaa ggggggaaaa tggggaggga 3171 aaaaaaaaaa cagcaacgga ggtttttgtg acaactaacc agaacaaaca gaagtcagct 3231 attaaaatat gtctaaatgt aatatctacc agcattcagt aactgttaat aacttcagtg 3291 atgcattcaa aaatgtgctt tgtcagaata agaatgccaa aaatgttttt tcgctgcctt 3351 atctcatacc agtttttttg ggtttttttt tgtttgtttg ttttttggtt tttttttttt 3411 tgtgtgtgtt gttatttggt tttctttttg cccacagttt gtctcaggca atactgggac 3471 ataggctgac cccattagct tttgttatga atttactaaa ctttctgtgg aaggagaaca 3531 gagcctctgc cgcgggtgtg gggaagccat cctgtgcttg aggcagcaca cgtgtgtcca 3591 tcatcatcag tcagaagagc agggcctgtc tcacccaatc gagtccttaa gacagaataa 3651 tcagaatggt cagagggaca gaccaatcaa ttcccaggaa agcaaaagtg actcaatgtc 3711 ccttgactcc caaatggtcc cactggactg gtgatcactg gtgacaacta actagctttg 3771 tccagagaat ccacccagaa cacggtgctt tttagccagt agtccacctc tatgtgcatc 3831 agcaatgcat agcaggtgag aacttgaatc acagaaactt catgccatgg atggagactc 3891 ctgaggcgct caaatactac tacctctagt tccaaagact agagctagat gatcagaaag 3951 gcaactggag gcccagggag ccgtactggg acaagttaga attagagaac gatgtcattt 4011 aacattccga gaaagaaata accatgaatt gctattacag gagtaacaca cagggccagc 4071 ttcttttttc ttctttttta tttttctttt cttattgtga gcagagggaa ttcacctcag 4131 ttcatctttc tctcagtact tttctttcaa gatatcaatc ctttatgact cttttgcttt 4191 taattctctc tctctctctc tctctctctc tctctctttc tctcaaagga gaggtttcag 4251 ttctaacaag ctaccatagt cctattaaag ccattttttt ttttagaata ttaaaagtcc 4311 aaactctctt gccaaactct ttcttcacat gcgcattggc tgaaaacaga atttacaaga 4371 atttctttag gaagaaactg gggatgtggc ccattggtca caaagttttt ttgtttgttt 4431 ttgtttttgt ttcaattctt gtttgattta tggacaatct ttggtttgta ttgctctgga 4491 gaaattggaa atcattgcag agtgaagata aatcagggca ccatgtatag tagagaatgt 4551 ttcagtagtt ttccaaacga gaacacaatt gcacactgta aacaacagga gtgtgaagga 4611 ccacagtctt gaggagttct tgttgccctg tgtttggtga aggcgttggg gaccgaggaa 4671 gacaacatac agtttggcca aggctctcag aggcttgctg tggcgccaat tcaagtatta 4731 caatgttgca tgctgtagaa agtagctgtt gctgttgttt tgttttgttt taatttaagt 4791 caccaaggca ctgttttatt cttttgtaaa aaaaaaaaaa gttcactgtg cacttataga 4851 gaaaataatc aacaatgttg tgaatttttg agaagacttt tttttttttg ataaaccaaa 4911 gatttagaaa tcattccatt gtcaacttgt aaaaaaaaaa aaaaaaaa 4959 <210> 2 <211> 807 <212> PRT
<213> Mus musculus <400> 2 Met Asp Ser Ser Val Lys Glu Ala Ile Lys Gly Thr Glu Val Ser Leu Ser Lys Ala Ala Asp Ala Phe Ala Phe Glu Asp Asp Ser Ser Arg Asp Gly Leu Ser Pro Asp Gln Ala Arg Ser Glu Asp Pro Gln Gly Ser Thr Gly Ser Thr Pro Asp,Ile Lys Ser Thr Glu Ala Pro Leu Asp Thr Ile Gln Asp Leu Thr Pro Gly Ser Glu Ser Asp Lys Asn Asp Ala Ala Ser Gln Pro Gly Asn Gln Ser Asp Pro Gly Lys Gln Val Leu Gly Pro Leu Ser Thr Pro Ile Pro Val His Thr Ala Val Lys Ser Lys Ser Leu Gly Asp Ser Lys Asn Arg His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu Lys Ser Pro Pro Pro Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Arg Phe Ser Tyr Pro Gly Met His Gln Thr His Leu Lys Glu Pro Asn Glu Gln Met Ala Arg Asn Pro Asn Pro Ser Ser Thr Pro Leu Ser Asn Thr Pro Leu Ser Pro Val Lys Asn Ser Ile Ser Gly Gln Thr Gly Val Ser Ser Leu Lys Pro Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys Val Ser Glu Leu Arg Gln Gln Leu Arg Ile Arg Gly Leu Pro Val Ser Gly Thr Lys Thr Ala Leu Val Asp Arg Leu Arg Pro Phe Gln Asp Cys Ala Gly Asn Pro Val Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe Pro Val Thr Pro Asn Thr Leu Pro Ser Tyr Gln Ser Ser Pro Thr Gly Phe Tyr His Phe Gly Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala Ser Ser Asp Leu Ser Ala Ala Gly Ser Leu Pro Asp Thr Phe Thr Asp Ala Ser Pro Gly Phe Gly Leu His Ala Ser Pro Val Pro Ala Cys Thr Asp Glu Ser Leu Leu Ser Ser Leu Asn Gly Gly Ser Gly Pro Ser Glu Pro Asp Gly Leu Asp Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln Lys Val Ile Asn Gln Leu Thr Trp Lys Leu Arg Gln Glu Gln Arg Gln Val Glu Glu Leu Arg Met Gln Leu Gln Lys Gln Lys Ser Ser Cys Ser Asp Gln Lys Pro Leu Pro Phe Leu Ala Thr Thr Ile Lys Gln Glu Asp Val Ser Ser Cys Pro Phe Ala Pro Gln Gln Ala Ser Gly Lys Gly Gln Gly His Ser Ser Asp Ser Pro Pro Pro Ala Cys Glu Thr Ala Gln Leu Leu Pro His Cys Val Glu Ser Ser Gly Gln Thr His Val Leu Ser Ser Thr Phe Leu Ser Pro Gln Cys Ser Pro Gln His Ser Pro Leu Gly Gly Leu Lys Ser Pro Gln His Ile Ser Leu Pro Pro Ser Pro Asn Asn His Tyr Phe Leu Ala Ser Ser Ser Gly Ala Gln Arg Glu Asn His Gly Val Ser Ser Pro Ser Ser Ser Gln Gly Cys Ala Gln Met Thr Gly Leu Gln Ser Ser Asp Lys Val Gly Pro Thr Phe Ser Ile Pro Ser Pro Thr Phe Ser Lys Ser Ser Ser Ala Val Ser Asp Ile Thr Gln Pro Pro Ser Tyr Glu Asp Ala Val Lys Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu g Leu Leu Asp Val Leu Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg Glu Asp His Ser Cys Leu Gln Lys Ile Pro Lys Ile Pro Gly Ser Ser Cys Ser Pro Thr Ala Ile Pro Pro Lys Pro Ser Ala Ser Phe Glu Gln Ala Ser Ser Gly Gly Gln Met Ala Phe Asp His Tyr Ala Asn Asp Ser Asp Glu His Leu Glu Val Leu Leu Asn Ser His Ser Pro Ile Gly Lys Val Ser Asp Val Thr Leu Leu Lys Ile Gly Ser Glu Glu Pro Pro Phe Asp Ser Ile Met Asp Gly Phe Pro Gly Lys Ala Ala Glu Asp Leu Phe Ser Ala His Glu Leu Leu Pro Gly Pro Leu Ser Pro Met His Ala Gln Leu Ser Pro Pro Ser Val Asp Ser Ser Gly Leu Gln Leu Ser Phe Thr Glu Ser Pro Trp Glu Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Ser Ser Thr Pro Gly Phe Ser Asn Leu Thr Ser Ser Gly Pro Ser Ile Phe Asn Ile Asp Phe Leu Asp Val Thr Asp Leu Asn Leu Asn Ser Pro Met Asp Leu His Leu Gln Gln Trp <210> 3 <211> 3907 <212 > DNA
<213> Mus musculus <220>
<221> CDS
<222> (5)..(2083) <400> 3 ccaa ggg atc atg ccg cct ttg aaa agt cca gcc gca ttt cat gag cag 49 Gly Ile Met Pro Pro Leu Lys Ser Pro Ala Ala Phe His Glu Gln aga agg agc ttg gag cgg gcc agg aca gag gac tat ctc aaa cgg aag 97 Arg Arg Ser Leu Glu Arg Ala Arg Thr Glu Asp Tyr Leu Lys Arg Lys att cgt tcc cgg ccg gag aga tcg gag ctg gtc agg atg cac att ttg 145 Ile Arg Ser Arg Pro Glu Arg Ser Glu Leu Val Arg Met, His Ile Leu gaa gag acc tcg get gag cca tcc ctc cag gcc aag cag ctg aag ctg 193 Glu Glu Thr Ser Ala Glu Pro Ser Leu Gln Ala Lys Gln Leu Lys Leu aag aga gcc aga cta gcc gat gac ctc aat gag aag att gca cag agg 241 Lys Arg Ala Arg Leu Ala Asp Asp Leu Asn Glu Lys Ile Ala Gln Arg cct ggc ccc atg gag ctg gtg gag aag aac atc ctt cct gtt gag tcc 289 Pro Gly Pro Met Glu Leu Val Glu Lys Asn Ile Leu Pro Val Glu Ser agc ctg aag gaa gcc atc att gtg ggc cag gtg aac tat ccc aaa gta 337 Ser Leu Lys Glu Ala Ile Ile Val Gly Gln Val Asn Tyr Pro Lys Val gca gac agc tct tcc ttc gat gag gac agc agc gat gcc tta tcc ccc 385 Ala Asp Ser Ser Ser Phe Asp Glu Asp Ser Ser Asp Ala Leu Ser Pro gag cag cct gcc agc cat gag tcc cag ggt tct gtg ccg tca ccc ctg 433 Glu Gln Pro Ala Ser His Glu Ser Gln Gly Ser Val Pro Ser Pro Leu gag gcc cga gtc agc gaa cca ctg ctc agt gcc acc tct gca tcc ccc 481 Glu Ala Arg Val Ser Glu Pro Leu Leu Ser Ala Thr Ser Ala Ser Pro acc cag gtt gtg tct caa ctt ccg atg ggc cgg gat tcc aga gaa atg 529 Thr Gln Val Val Ser Gln Leu Pro Met Gly Arg Asp Ser Arg Glu Met ctt ttc ctg gca gag cag cct cct ctg cct ccc cca cct ctg ctg cct 577 Leu Phe Leu Ala Glu Gln Pro Pro Leu Pro Pro Pro Pro Leu Leu Pro ccc agc ctc acc aat gga acc act atc ccc act gcc aag tcc acc ccc 625 Pro Ser Leu Thr Asn Gly Thr Thr Ile Pro Thr Ala Lys Ser Thr Pro aca ctc att aag caa agc caa ccc aag tct gcc agt gag aag tca cag 673 Thr Leu Ile Lys Gln Ser Gln Pro Lys Ser Ala Ser Glu Lys Ser Gln cgc agc aag aag gcc aag gag ctg aag cca aag gtg aag aag ctc aag 721 Arg Ser Lys Lys Ala Lys Glu Leu Lys Pro Lys Val Lys Lys Leu Lys tac cac cag tac atc ccc ccg gac cag aag cag gac agg ggg gca ccc 769 Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Gln Asp Arg Gly Ala Pro ccc atg gac tca tcc tac gcc aag atc ctg cag cag cag cag ctc ttc 817 Pro Met Asp Ser Ser Tyr Ala Lys Ile Leu Gln Gln Gln Gln Leu Phe ctc cag ctg cag atc ctc aac cag cag cag cag cag cac cac aac tac 865 Leu Gln Leu Gln Ile Leu Asn Gln Gln Gln Gln Gln His His Asn Tyr cag gcc atc ctg cct gcc ccg cca aag tca gca ggc gag gcc ctg gga 913 Gln Ala Ile Leu Pro Ala Pro Pro Lys Ser Ala Gly Glu Ala Leu Gly agc agc ggg acc ccc cca gta cgc agc ctc tcc act acc aat agc agc 961 Ser Ser Gly Thr Pro Pro Val Arg Ser Leu Ser Thr Thr Asn Ser Ser tcc agc tcg ggc gcc cct ggg ccc tgt ggg ctg gca cgt cag aac agc 1009 Ser Ser Ser Gly Ala Pro Gly Pro Cys Gly Leu Ala Arg Gln Asn Ser acc tca ctg act ggc aag ccg gga gcc ctg ccg gcc aac ctg gac gac 1057 Thr Ser Leu Thr Gly Lys Pro Gly Ala Leu Pro Ala Asn Leu Asp Asp atg aag gtg gca gag ctg aag cag gag ctg aag ttg cga tca ctg cct 1105 Met Lys Val Ala Glu Leu Lys Gln Glu Leu Lys Leu Arg Ser Leu Pro gtc tcg ggc acc aaa act gag ctg att gag cgc ctt cga gcc tat caa 1153 Val Ser Gly Thr Lys Thr Glu Leu Ile Glu Arg Leu Arg Ala Tyr Gln gac caa atc agc cct gtg cca gga gcc ccc aag gcc cct gcc gcc acc 1201 Asp Gln Ile Ser Pro Val Pro Gly Ala Pro Lys Ala Pro Ala Ala Thr tct atc ctg cac aag get ggc gag gtg gtg gta gcc ttc cca gcg gcc 1249 Ser Ile Leu His Lys Ala Gly Glu Val Val Val Ala Phe Pro Ala Ala cgg ctg agc acg ggg cca gcc ctg gtg gca gca ggc ctg get cca get 1297 Arg Leu Ser Thr Gly Pro Ala Leu Val Ala Ala Gly Leu Ala Pro Ala gag gtg gtg gtg gcc acg gtg gcc agc agt ggg gtg gtg aag ttt ggc 1345 Glu Val Val Val Ala Thr Val Ala Ser Ser Gly Val Val Lys Phe Gly agc acg ggc tcc acg ccc ccc gtg tct ccc acc ccc tcg gag cgc tca 1393 Ser Thr Gly Ser Thr Pro Pro Val Ser Pro Thr Pro Ser Glu Arg Ser ctg ctc agc acg ggc gat gaa aac tcc acc ccc ggg gac acc ttt ggt 1441 Leu Leu Ser Thr Gly Asp Glu Asn Ser Thr Pro Gly Asp Thr Phe Gly gag atg gtg aca tca cct ctg acg cag ctg acc ctg cag gcc tcg cca 1489 Glu Met Val Thr Ser Pro Leu Thr Gln Leu Thr Leu Gln Ala Ser Pro ctg cag atc ctc gtg aag gag gag ggc ccc cgg gcc ggg tcc tgt tgc 1537 Leu Gln Ile Leu Val Lys Glu Glu Gly Pro Arg Ala Gly Ser Cys Cys ctg agc cct ggg ggg cgg gcg gag cta gag ggg cgc gac aag gac cag 1585 Leu Ser Pro Gly Gly Arg Ala Glu Leu Glu Gly Arg Asp Lys Asp Gln atg ctg cag gag aaa gac aag cag atc gag gcg ctg acg cgc atg ctc 1633 Met Leu Gln Glu Lys Asp Lys Gln Ile Glu Ala Leu Thr Arg Met Leu cgg cag aag cag cag ctg gtg gag cgg ctc aag ctg cag ctg gag cag 1681 Arg Gln Lys Gln Gln Leu Val Glu Arg Leu Lys Leu Gln Leu Glu Gln gag aag cga gcc cag cag ccc gcc ccc gcc ccc gcc ccc ctc ggc acc 1729 Glu Lys Arg Ala Gln Gln Pro Ala Pro Ala Pro Ala Pro Leu Gly Thr ccc gtg aag cag gag aac agc ttc tcc agc tgc cag ctg agc cag cag 1777 Pro Val Lys Gln Glu Asn Ser Phe Ser Ser Cys Gln Leu Ser Gln Gln ccc ctg ggc ccc get cac cca ttc aac ccc agc ctg gcg gcc cca gcc 1825 Pro Leu Gly Pro Ala His Pro Phe Asn Pro Ser Leu Ala Ala Pro Ala acc aac cac ata gac cct tgt get gtg gcc ccg ggg ccc ccg tcc gtg 1873 Thr Asn His Ile Asp Pro Cys Ala Val Ala Pro Gly Pro Pro Ser Val gtg gtg aag cag gaa gcc ttg cag cct gag ccc gag ccg gtc ccc gcc 1921 Val Val Lys Gln Glu Ala Leu Gln Pro Glu Pro Glu Pro Val Pro Ala ccc cag ttg ctt ctg ggg cct cag ggc ccc agc ctc atc aag ggg gtt 1969 Pro Gln Leu Leu Leu Gly Pro Gln Gly Pro Ser Leu Ile Lys Gly Val gca cct ccc acc ctc atc acc gac tcc aca ggg acc cac ctt gtc ctc 2017 Ala Pro Pro Thr Leu Ile Thr Asp Ser Thr Gly Thr His Leu Val Leu acc gtg acc aat aag aat gca gac agc cct ggc ctg tcc agt ggg agc 2065 Thr Val Thr Asn Lys Asn Ala Asp Ser Pro Gly Leu Ser Ser Gly Ser ccc cag cag ccc tcg tcc cagcctggct ctccagcgcc tgccccctct 2113 Pro Gln Gln Pro Ser Ser gcccagatgg acctggagca cccactgcag cccctctttg ggacccccac ttctctgctg 2173 aagaaggaac cacctggcta tgaggaagcc atgagccagc agcccaaaca gcaggaaaat 2233 ggttcctcaa gccagcagat ggacgacctg tttgacattc tcattcagag cggagaaatt 2293 tcagcagatt tcaaggagcc gccatccctg ccagggaagg agaagccatc cccgaagaca 2353 gtctgtgggt cccccctggc agcacagcca tcaccttctg ctgagctccc ccaggctgcc 2413 ccacctcctc caggctcacc ctccctccct ggacgcctgg aggacttcct ggagagcagc 2473 acggggctgc ccctgctgac cagtgggcat gacgggccag agcccctttc cctcattgac 2533 gacctccata gccagatgct gagcagcact gccatcctgg accacccccc gtcacccatg 2593 gacacctcgg aattgcactt tgttcctgag cccagcagca ccatgggcct ggacctggct 2653 gatggccacc tggacagcat ggactggctg gagctgtcgt caggtggtcc cgtgctgagc 2713 ctagcccccc tcagcaccac agcccccagc ctcttctcca cagacttcct cgatggccat 2773 gatttgcagc tgcactggga ttcctgcttg tagctctctg gctcaagacg gggtggggaa 2833 ggggctggga gccagggtac tccaatgcgt ggctctcctg cgtgattcgg cctctccaca 2893 tggttgtgag tcttgacaat cacagcccct gctttttccc ttccctggga ggctagaaca 2953 gagaagccct tactcctggt tcagtgccac gcagggcaga ggagagcagc tgtcaagaag 3013 cagccctggc tctcacgctg gggttttgga cacacggtca gggtcagggc catttcagct 3073 tgacctcctt ttttgaggtc agggggcact gtctgtctgg ctacaatttg gctaaggtag 3133 gtgaagcctg gccaggcggg aggcttctct tctgacccag ggctgagaca ggttaagggg 3193 tgaatctcct tcctttctct ccctgctttg ctgtgaaggg agaaattagc ctgggcctct 3253 accccctatt ccctgtgtct gccaacccca ggatcccagg gctccctgcc attttagtgt 3313 cttggtgtag tgtaaccatt tagtggttgg tggcaacaat tttatgtaca ggtgtatata 3373 cctctatatt atatatcgac atacatatat atttttgggg gggggcggac aggagatggg 3433 tgcaactccc tcccatccta ctctcacaga agggcctgga tgcaaggtta cccttgagct 3493 gtgtgccaca gtctggtgcc cagtctggca tgcagctacc caggcccacc catcacgtgt 3553 gattgacatg taggtaccct gccacggcct atgccccacc tgccctgctt cctggctcct 3613 tatcagtgcc atgagggcag aggtgctacc tggccttcct gccaggagct ctccacccac 3673 tcacattccg tccccgccgc ctcactgcag ccagcgtggt cctaggacag gaggagcttc 3733 gggcccagct tcaccctgcg gtggggctga ggggtggcca tctcctgccc tggggccact 3793 ggcttcacat tctgggctga ctcatagggg agtaggggtg gagtcaccaa aaccagtgct 3853 gggacaaaga tggggaaggt gtgtgaactt tttaaaataa acacaaaaac acag 3907 <210> 4 <211> 693 <212> PRT
<213> Mus musculus <400> 4 Gly Ile Met Pro Pro Leu Lys Ser Pro Ala Ala Phe His Glu Gln Arg Arg Ser Leu Glu Arg Ala Arg Thr Glu Asp Tyr Leu Lys Arg Lys Ile Arg Ser Arg Pro Glu Arg Ser Glu Leu Val Arg Met His Ile Leu Glu Glu Thr Ser Ala Glu Pro Ser Leu Gln Ala Lys Gln Leu Lys Leu Lys Arg Ala Arg Leu Ala Asp Asp Leu Asn Glu Lys Ile Ala Gln Arg Pro Gly Pro Met Glu Leu Val Glu Lys Asn Ile Leu Pro Val Glu Ser Ser Leu Lys Glu Ala Ile Ile Val Gly Gln Val Asn Tyr Pro Lys Val Ala Asp Ser Ser Ser Phe Asp Glu Asp Ser Ser Asp Ala Leu Ser Pro Glu Gln Pro Ala Ser His Glu Ser Gln Gly Ser Val Pro Ser Pro Leu Glu Ala Arg Val Ser Glu Pro Leu Leu Ser Ala Thr Ser Ala Ser Pro Thr Gln Val Val Ser Gln Leu Pro Met Gly Arg Asp Ser Arg Glu Met Leu Phe Leu Ala Glu Gln Pro Pro Leu Pro Pro Pro Pro Leu Leu Pro Pro Ser Leu Thr Asn Gly Thr Thr Ile Pro Thr Ala Lys Ser Thr Pro Thr Leu Ile Lys Gln Ser Gln Pro Lys Ser Ala Ser Glu Lys Ser Gln Arg Ser Lys Lys Ala Lys Glu Leu Lys Pro Lys Val Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Gln Asp Arg Gly Ala Pro Pro Met Asp Ser Ser Tyr Ala Lys Ile Leu Gln Gln Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Asn Gln Gln Gln Gln Gln His His Asn Tyr Gln Ala Ile Leu Pro Ala Pro Pro Lys Ser Ala Gly Glu Ala Leu Gly Ser Ser Gly Thr Pro Pro Val Arg Ser Leu Ser Thr Thr Asn Ser Ser Ser Ser Ser Gly Ala Pro Gly Pro Cys Gly Leu Ala Arg Gln Asn Ser Thr Ser Leu Thr Gly Lys Pro Gly Ala Leu Pro Ala Asn Leu Asp Asp Met Lys Val Ala Glu Leu Lys Gln Glu Leu Lys Leu Arg Ser Leu Pro Val Ser Gly Thr Lys Thr Glu Leu Ile Glu Arg Leu Arg Ala Tyr Gln Asp Gln Ile Ser Pro Val Pro Gly Ala Pro Lys Ala Pro Ala Ala Thr Ser Ile Leu His Lys Ala Gly Glu Val Val Val Ala Phe Pro Ala Ala Arg Leu Ser Thr Gly Pro Ala Leu Val Ala Ala Gly Leu Ala Pro Ala Glu Val Val Val Ala Thr Val Ala Ser Ser Gly Val Val Lys Phe Gly Ser Thr Gly Ser Thr Pro Pro Val Ser Pro Thr Pro Ser Glu Arg Ser Leu Leu Ser Thr Gly Asp Glu Asn Ser Thr Pro Gly Asp Thr Phe Gly Glu Met Val Thr Ser Pro Leu Thr Gln Leu Thr Leu Gln Ala Ser Pro Leu IS

Gln Ile Leu Val Lys Glu Glu Gly Pro Arg Ala Gly Ser Cys Cys Leu Ser Pro Gly Gly Arg Ala,Glu Leu Glu Gly Arg Asp Lys Asp Gln Met Leu Gln Glu Lys Asp Lys Gln Ile Glu Ala Leu Thr Arg Met Leu Arg Gln Lys Gln Gln Leu Val Glu Arg Leu Lys Leu Gln Leu Glu Gln Glu Lys Arg Ala Gln Gln Pro Ala Pro Ala Pro Ala Pro Leu Gly Thr Pro Val Lys Gln Glu Asn Ser Phe Ser Ser Cys Gln Leu Ser Gln Gln Pro Leu Gly Pro Ala His Pro Phe Asn Pro Ser Leu Ala Ala Pro Ala Thr Asn His Ile Asp Pro Cys Ala Val Ala Pro Gly Pro Pro Ser Val Val Val Lys Gln Glu Ala Leu Gln Pro Glu Pro Glu Pro Val Pro Ala Pro 625 630 635. 640 Gln Leu Leu Leu Gly Pro Gln Gly Pro Ser Leu Ile Lys Gly Val Ala Pro Pro Thr Leu Ile Thr Asp Ser Thr Gly Thr His Leu Val Leu Thr Val Thr Asn Lys Asn Ala Asp Ser Pro Gly Leu Ser Ser Gly Ser Pro Gln Gln Pro Ser Ser <210> 5 <211> 35 <212> PRT
<213> Mus musculus <400> 5 Leu Glu Lys Met Lys Val Ser Asp Leu Lys Gln His Leu Lys Arg Arg Asn Leu Pro Val Ser Gly Pro Lys Pro His Leu Ile Glu Arg Leu Lys Pro Tyr Leu <210> 6 <211> 6459 <212> DNA
<213> Mus musculus <220>
<221> CDS
<222> (1)..(1053) <400> 6 cag act tca cca caa gca gga atg cag act cag cct cag ata gca act 48 Gln Thr Ser Pro Gln Ala Gly Met Gln Thr Gln Pro Gln Ile Ala Thr get gca caa ata cca act get gcc ttg gcc tca ggc ttg gcc cca act 96 Ala Ala Gln Ile Pro Thr Ala Ala Leu Ala Ser Gly Leu Ala Pro Thr gta cct cag aca caa gac acg ttc ccg cag cat gtg ctc agt cag cct 144 Val Pro Gln Thr Gln Asp Thr Phe Pro Gln His Val Leu Ser Gln Pro caa caa gtc aga aag gtt ttc aca aac tca gca tca tca aat aca gtt 192 Gln Gln Val Arg Lys Val Phe Thr Asn Ser Ala Ser Ser Asn Thr Val ctt cca tat cag aga cat cct gcc cca get gtc cag cag ccc ttt atc 240 Leu Pro Tyr Gln Arg His Pro Ala Pro Ala Val Gln Gln Pro Phe Ile aat aag gcc tcc aac agt gtt ctt caa tcc aga aat get ccg ctt cca 288 Asn Lys Ala Ser Asn Ser Val Leu Gln Ser Arg Asn Ala Pro Leu Pro tcc ctg caa aat gga cct aac aca ccc aac aag cct agt tca ccc ccg 336 Ser Leu Gln Asn Gly Pro Asn Thr Pro Asn Lys Pro Ser Ser Pro Pro cca ccc cag caa ttt gtc gtc cag cac tct cta ttt ggg agt cca gtc 384 Pro Pro Gln Gln Phe Val Val Gln His Ser Leu Phe Gly Ser Pro Val gcc aag aca aaa gat ccc ccc cgc tat gag gag gcc atc aag cag aca 432 Ala Lys Thr Lys Asp Pro Pro Arg Tyr Glu Glu Ala Ile Lys Gln Thr cgc agc aca cag gcc cct ctg cca gag att tcc aac get cac agt cag 480 Arg Ser Thr Gln Ala Pro Leu Pro Glu Ile Ser Asn Ala His Ser Gln cag atg gat gac ctc ttt gat atc ctc att aag agt gga gag atc tcc 528 Gln Met Asp Asp Leu Phe Asp Ile Leu Ile Lys Ser Gly Glu Ile Ser ctc ccc ata aaa gaa gaa cct tct cct att tcc aaa atg aga cca gtg 576 Leu Pro Ile Lys Glu Glu Pro Ser Pro Ile Ser Lys Met Arg Pro Val aca gcc agc atc acc aca atg cca gtg aat aca gtg gtg tcc cgg cca 624 Thr Ala Ser Ile Thr Thr Met Pro Val Asn Thr Val Val Ser Arg Pro cca ccc caa gtc caa atg gca cca cct gta tct tta gaa cct atg ggc 672 Pro Pro Gln Val Gln Met Ala Pro Pro Val Ser Leu Glu Pro Met Gly agt tta tct gcc agc tta gag aac caa cta gaa get ttc ttg gat gga 720 Ser Leu Ser Ala Ser Leu Glu Asn Gln Leu Glu Ala Phe Leu Asp Gly act tta ccc tca gcc aat gaa att cct cca cta caa agc agc agt gaa 768 Thr Leu Pro Ser Ala Asn Glu Ile Pro Pro Leu Gln Ser Ser Ser Glu gac aga gag ccc ttc tct ctg atc gag gac ctc cag aat gat ctg ctg 816 Asp Arg Glu Pro Phe Ser Leu Ile Glu Asp Leu Gln Asn Asp Leu Leu agt cac tca ggt atg ctg gac cat tca cac tca ccc atg gag act tcc 864 Ser His Ser Gly Met Leu Asp His Ser His Ser Pro Met Glu Thr Ser gag acc cag ttt get gca ggt act ccc tgt ctg tct ctc gac ctg tca 912 Glu Thr Gln Phe Ala Ala Gly Thr Pro Cys Leu Ser Leu Asp Leu Ser gac tca aac ttg gac aac atg gag tgg ttg gac att acc atg ccc aac 960 Asp Ser Asn Leu Asp Asn Met Glu Trp Leu Asp Ile Thr Met Pro Asn tcc tct tca gga ctc act cct ctc agc acc acc gcg ccg agc atg ttc 1008 Ser Ser Ser Gly Leu Thr Pro Leu Ser Thr Thr Ala Pro Ser Met Phe tct get gac ttt cta gac cca cag gac cta ccg ctg cca tgg gac 1053 Ser Ala Asp Phe Leu Asp Pro Gln Asp Leu Pro Leu Pro Trp Asp taacgtcaca gatttctttt ctgagagttg atgaggttta agaacatgaa gattctaaaa 1113 ggtcagtttt tagagataga tctatagttg cattgttgca atcaaaatat gttgtcacag 1173 aaagaatagg tggaaggtca tagcctggaa cccaagtttg aaaacatttc attgtgttca 1233 gtagtgaatt tctacagttt aacatagcac agggccttct gaaaatcgca cttgtcaaag 1293 acgactcatc tatttctcca gacttcagta aagaatgaaa agtaccttta gataaaaaca 1353 aagaagagta atatatgcag cacagtgacg ttaggattct ggtaattaac tacatttaaa 1413 tctctggtca ctttaagacc ctaaataaaa ggcagacagc tccactcaaa aactaaggct 1473 gatgtgaggg aggtgagagg tcactgcact tggtacttcc tagagacggc cggagccagg 1533 cccaagacac agcagaggtc aaaggcagtg gagagccttg gccagttcag tgacagcttc 1593 tggctgaaga cttttggttc tattcagaaa cctgtgtcgt ttttttggtg ttgtagttta 1653 ttttgtgatt ttttggaatc gtactttata tttccaaatt taaatttaaa tgcaagatct 1713 ttcaacataa acagaagata cctacaaaat actgtcagaa gtccaggtat actgataaca 1773 ctgaaaattc tattagcaac cttctgggtt ggttagattg attttaatgt atatattaga 1833 catttgtatg tatgctctga cattgtgatt tgtacagcct accaaccaat ctaactaaaa 1893 ttacatatat aatctgtaaa catacatacg agactgtaac actaaacatg tcggatggct 1953 ggggtaagga aatgggtatc caaggtccta cttttttaat agctcgaata tttctagagt 2013 acttgagcca catgtatttc tgtatttaaa gaattgctga ctaactttca ggtaaccaga 2073 cccatctcaa agaaccaaga aaaggcttta gcatgaaata tctttctgag ctggcgagtt 2133 agaagaatgg aaggtaaggg gaaggtctgt catctaccca ggacattccc atgatgagta 2193 caggtcagat tgtgccacaa ggtgggcctc cacgtccctg ccctggccct ctttcttctg 2253 tcactaaccc tggttatcat tttacaggct tgtaactgga tattctacca gagctctcac 2313 tatattgtca agcctaagat tgaaaaactg gaggctttat tagtgttttt atatagaaaa 2373 cagttattac atatgtgtta agtcatttct taagaatttt ctaaaatgcc aactatcaca 2433 ggattatttc aagctagtca ttgaggtata tgacaaaatg taaataacaa aaaactgaaa 2493 tctaccaaaa gagcatggag atttttctta aataataata ttgtgctctc cacctcaccc 2553 ttgtgtaaac cctcaggtca ggttggttcc cctgggtcac aaaatggtaa atgttccata 2613 ctgacatgcc ggaggcagcc tgacccgtta tttggaaaga atttgtgaat tatttctggg 2673 tttgtgtttt gcctaagagc tgatcttatt tctgatttgt gtgtgtgtgg tttataaatt 2733 ttactacgtg taacaaaagt ctgcttttcc agcatgagca cactggagcc ctctgctcac 2793 tggcacttcc tgactcaaag gcactaacag tgctcatgtg ccttccagac ggttcaaggc 2853 agaggccact gtgctcagtg tagtctgtga tgaatagttt aagtgttcag aaattggtaa 2913 accaacacac gggatacaat aactctctgt taaccagaac accgtcattt gaccaagccc 2973 1~

tacaagagtt taccacacta gatgttctgt gaatcctcga gtcagttcca ttgagagggg 3033 cctgtctcca gggccaggct atttacttgg gaaagtattt ttcttacagt tcttggccac 3093 agtttttttg ctgagggttt ctgtctgggc ctatcaggtc catacttaga ccctgagcat 3153 cttcttcatt cagatttgaa tggcttatta aattagcacc aaatatcagt gggactgtag 3213 aaggtaaccg aacactagta ccattgactc tcgttgaata actttatatt tccataatcc 3273 tgaattgtgt agatagtttt ctagctctcg ggtcccttta ttgcttttta aaatagggtt 3333 Egaaacatgc cacaggaagg ttgctctcca aaaatacaca gtgcagtgca agaaaatgct 3393 atctcattgg cctactctcc tatgaattgc taaagtgccc acttcacata tgtgtttaaa 3453 cctttataaa ccagtatttc acttttaaaa agacaaggca tctctaccca ttaactctgc 3513 aagccactcc acttgcacca ttccgcttga ccctcctctc tcctggcttg ggtcaccagc 3573 caggcacctg tgacacgagt gctgctctcc aggatctcca ctacatgttc caggttggag 3633 ' tgaggacgcg ctatgtgctc acactcatgt gacatgacca aagatgatac tctgtaaaca 3693 aggcccttct gaccggactc agtgcgtgtg atggtgagtg caatgaggaa gggtggatat 3753 tgactaaaga ctggttgttg ttgttgttta ggttagtgtc acagccatta cagcacaagt 3813 caaagtcgcc agttgaattt tcattatgca cgtgtgtggt ttaagcagtg gtactgttgt 3873 atatcatatt gtaaagtatc atactgccaa gaaaataact cctagaaagg cattatctca 3933 catccccatc ttactttcct acatgttctc aaaacacagt agtaccagcc ttacctttct 3993 gctgtatgta gatagtcaga tcatcctact gggggtggga tgaatttaaa agttatacca 4053 aaatttctgt aaagtctttg aaagtctagg agtaggtggt catcttgtac atttcagcaa 4113 agcatccact aggaaacctc ataggacagt gttagtggtt cacgttctag tgtttttcct 4173 gaaatgtgca atctactgta tagtattgcc acataattgt acatagatgt attctgaatt 4233 tgtggaattt cttgcttaga tactattgtg tttgtttcat atgaatattt ttgtaattct 4293 aaaagagatc ttatttaaat ttccttttta aaagccgcat ggttctgtga tccatgtaac 4353 tgacactttt tggctttcag tgctgtttag aaacagtggc aaaggcaggg tggtgctgcc 4413 tgcaagctgc tgcctatgga aggcaaagtc atagtaatga gatagcacct ctgaactgtg 4473 cagtcagcat accctgagtg atggctcagg ggcgcactac ctattttgtc accagagctg 4533 actcaggctt cctggaccct caaccccaga tcattccagg cagcatagct ttcttcacag 4593 tcctttcaga attcccaggc tgaaatcagc catagcagtt gacaaaacag ctatccccac 4653 aagtgatgag atagtccctt tactgtcctc aaatggactt ggccttagag acgtggtaaa 4713 gcactttggc agggtttaaa atatttgtga gaagcccaca tttcagtata catcctcact 4773 ggcttccatg cacccacctg acggtagcct cacagaagtc ctggctgtca ctcaggtggg 4833 gagctcatgg tgccgctggg gactttttag agaaatgtaa agagaatagc tattcagtgt 4893 ctactagcag agcaacatgt gtcaatttaa ccaaattcac aaataaccct ccatttttca 4953 atatctgcta ctgtaaacat gaatattgaa tactgacaag agaataccca tacaaatcgt 5013 cccaccgccc tagaggccac agaattagcc caaaattatc aaagaacatt aactggaagg 5073 tcaggttttt caaggaacat agcttacaaa tgcatcagtg tgtatctgga gagcatccta 5133 actgcatttc aactcatctt ttaagtgatt tcagtcaaaa ctggaaaaca actaagatgt 5193 agtaattttt ttttcctggt tcaaaccttc aataacttgc tcattcagca gtctctctga 5253 gctacatttt tatttgtaaa gtgactctgt ctgcatggca atgagcaggt gcgtgttttt 5313 tccacattcg ccctttcttg cagtatccag ggaaacacat cattacaaag ggtttctacc 5373 tgaaatcttt catggaaggc ctacaattcg aaaagctgca catgtttaca gaagagctct 5433 taccctccat gcaaacactt tgctctgtgg tgtcacagct ttgtgacaat aagatggcaa 5493 tctcggatct acaaggtgct gtcgggaatc aaataaaata tgttatcaga gatatcatca 5553 catctatagt gtttaacaga gctttatgcc aactactaag acaaagcttt aacaaagttt 5613 atagaatact gaaactcgta acaattacct ctctacgtga tgctgtaagg aatcttgcta 5673 atttggtagg aagaggaagc atttaggaaa gggtttagta tctaccaaaa gtacttgacc 5733 tcaagtaacc aatagtaatg caaacttgct ttaaaggaac caaaggcatt gccaagtatt 5793 tgccaaaagg aggcactttt tatttaaaat ttgagactaa tgagatctca aaaatcagcc 5853 ccaaaaaggt attatccatt taaggttata attttcacta agatgtagat atttctctta 5913 ttgttttcat gtaaaatagt atagagttgt tttgttggtt taagagtaac attcagtagt 5973 aatacaaagt tttttttcta tgtagaaatt agttttcttt tcttgcttgc aatagaaatg 6033 caatgtgata ggtgtttctc ttcttatttt cattgtcaca ttatgtctta gcatctcact 6093 ttatgaaaaa aaggagaaag ataccaatct acagagccct gcttgttgaa gcactagttt 6153 aatcaacaaa aaattatggc aatcgggggt ccattcatct attgccttta tgttgttttt 6213 taaaagaaaa accatgatgc ctttgtattt gctgtttgca cccctgaaat caattccata 6273 tcatgtttga atgccataca ttttgcacat gtactgtaca taagtaatgc atactgtatt 6333 tttatatgtg tgcacattta tcatcagatc ttttgtacat agtggcagta ttgtagctga 6393 tcgggaaatg tttgatatct cagcaatttt gcatttttgt gtctcaaata aaagacattt 6453 tgatgt 6459 <210> 7 <211> 351 <212> PRT
<213> Mus musculus <400> 7 G1n Thr Ser Pro Gln Ala Gly Met Gln Thr Gln Pro Gln Ile Ala Thr Ala Ala Gln Ile Pro Thr Ala Ala Leu Ala Ser Gly Leu Ala Pro Thr Val Pro Gln Thr Gln Asp Thr Phe Pro Gln His Val Leu Ser Gln Pro Gln Gln Val Arg Lys Val Phe Thr Asn Ser Ala Ser Ser Asn Thr Val Leu Pro Tyr Gln Arg His Pro Ala Pro Ala Val Gln Gln Pro Phe Ile Asn Lys Ala Ser Asn Ser Val Leu Gln Ser Arg Asn Ala Pro Leu Pro Ser Leu Gln Asn Gly Pro Asn Thr Pro Asn Lys Pro Ser Ser Pro Pro Pro Pro Gln Gln Phe Val Val Gln His Ser Leu Phe Gly Ser Pro Val Ala Lys Thr Lys Asp Pro Pro Arg Tyr Glu Glu Ala Ile Lys Gln Thr Arg Ser Thr Gln Ala Pro Leu Pro Glu Ile Ser Asn Ala His Ser Gln Gln Met Asp Asp Leu Phe Asp Ile Leu Ile Lys Ser Gly Glu Ile Ser Leu Pro Ile Lys Glu Glu Pro Ser Pro Ile Ser Lys Met Arg Pro Val Thr Ala Ser Ile Thr Thr Met Pro Val Asn Thr Val Val Ser Arg Pro Pro Pro Gln Val Gln Met Ala Pro Pro Val Ser Leu Glu Pro Met Gly Ser Leu S°_r Ala Ser Leu Glu Asn Gln Leu Glu Ala Phe Leu Asp Gly Thr Leu Pro Ser Ala Asn Glu Ile Pro Pro Leu Gln Ser Ser Ser Glu Asp Arg Glu Pro Phe Ser Leu Ile Glu Asp Leu Gln Asn Asp Leu Leu Ser His Ser Gly Met Leu Asp His Ser His Ser Pro Met Glu Thr Ser Glu Thr Gln Phe Ala Ala Gly Thr Pro Cys Leu Ser Leu Asp Leu Ser Asp Ser Asn Leu Asp Asn Met Glu Trp Leu Asp Ile Thr Met Pro Asn Ser Ser Ser Gly Leu Thr Pro Leu Ser Thr Thr Ala Pro Ser Met Phe Ser Ala Asp Phe Leu Asp Pro Gln Asp Leu Pro Leu Pro Trp Asp <210> 8 <211> 35 <212> PRT
<213> Mus musculus <400> 8 Val Thr Lys Met Lys Val Ala Asp Leu Lys Arg Glu Leu Lys Leu Arg Gly Leu Ala Val Asn Gly Asn Lys Thr Glu Leu Gln Asp Arg Leu Gln Thr Ala Leu <210> 9 <211> 35 <212> PRT
<213> Mus musculus <400> 9 Leu Asp Asp Met Lys Val Ala Glu Leu Lys Gln Glu Leu Lys Leu Arg Ser Leu Pro Val Ser Gly Thr Lys Thr Glu Leu Ile Glu Arg Leu Arg Ala Tyr Gln <210> 10 <211> 35 <212> PRT
<213> Mus musculus <400> 10 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Asp Leu Met Glu Arg Leu Gln Ala Ala Leu <210> 11 <211> 35 <212> PRT
<213> Mus musculus <400> 11 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Glu Leu Met Glu Arg Leu Gln Ala Ala Leu <210> 12 <211> 35 <212> PRT
<213> Mus musculus <400> 12 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Asp Leu Met Asp Arg Leu Gln Ala Ala Leu <210> 13 <211> 35 <212> PRT
<213> Mus musculus <400> 13 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Asp Leu Met Asp Arg Leu Gln Ala Ala Leu <210> 14 <211> 35 <212> PRT
<213> Mus musculus <400> 14 Met Glu Gln Leu Lys Val Leu Glu Leu Lys Gln Ile Cys Lys Ser Leu Asp Leu Ser Ile Thr Gly Lys Lys Ala Val Leu Gln Asp Arg Ile Lys Gln Phe Leu <210> 15 <211> 35 <212> PRT
<213> Mus musculus <400> 15 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Asp Leu Met Asp Arg Leu Gln Ala Ala Leu <210> 16 <211> 35 <212> PRT
<213> Mus musculus <400> 16 Val Lys Lys Leu Lys Val Ser Glu Leu Lys Glu Glu Leu Lys Lys Arg Arg Leu Ser Asp Lys Gly Leu Lys Ala Asp Leu Met Asp Arg Leu Gln Ala Ala Leu <210> 17 <211> 35 <212> PRT
<213> Mus musculus <400> 17 Leu Gln Ala Leu Arg Val Thr Asp Leu Lys Ala Ala Leu Glu Gln Arg Gly Leu Ala Lys Ser Gly Gln Lys Ser Ala Leu Val Lys Arg Leu Lys Gly Ala Leu <210> 18 <211> 35 <212> PRT
<213> Mus musculus <400> 18 Leu Gln Ala Leu Arg Val Thr Asp Leu Lys Ala Ala Leu Glu Gln Arg Gly Leu Ala Lys Ser Gly Gln Lys Ser Ala Leu Val Lys Arg Leu Lys Gly Ala Leu <210> 19 <211> 35 <212> PRT
<213> Mus musculus <400> 19 Leu Ser Glu Leu Arg Val Ile Asp Leu Arg Ala Glu Leu Lys Lys Arg Asn Leu Asp Thr Gly Gly Asn Lys Ser Val Leu Met Glu Arg Leu Lys Lys Ala Val <210> 20 <211> 35 <212> PRT
<213> Mus musculus <400> 20 Leu Ser Asp Leu Arg Val Ile Asp Leu Arg Ala Glu Leu Arg Lys Arg Asn Val Asp Ser Ser Gly Asn Lys Ser Val Leu Met Glu Arg Leu Lys Lys Ala Ile <210> 21 <211> 35 <212> PRT
<213> Mus musculus <400> 21 Val Arg Arg Leu Lys Val Asn Glu Leu Arg Glu Glu Leu Gln Arg Arg Gly Leu Asp Thr Arg Gly Leu Lys Thr Glu Leu Ala Glu Arg Leu Gln Ala Ala Leu <210> 22 <211> 35 <212> PRT
<213> Mus musculus <400> 22 Ile Lys Ala Leu Lys Val Ser Gln Leu Lys Asp Ile Leu Arg Asp Arg Gly Leu Arg Val Ser Gly Lys Lys Ala Asp Leu Leu Asp Asn Leu Thr Asn Tyr Val <210> 23 <211> 35 <212> PRT
<213> Mus musculus <400> 23 Ala Asn Lys Leu Lys Val Asp Glu Leu Arg Leu Lys Leu Ala Glu Arg Gly Leu Ser Thr Thr Gly Val Lys Ala Val Leu Val Glu Arg Leu Glu Glu Ala Ile <210> 24 <211> 3907 <212> PRT
<213> Mus musculus <400> 24 Cys Cys Ala Ala Gly Gly Gly Ala Thr Cys Ala Thr Gly Cys Cys Gly Cys Cys Thr Thr Thr Gly Ala Ala Ala Ala Gly Thr Cys Cys Ala Gly Cys Cys Gly Cys Ala Thr Thr Thr Cys Ala Thr Gly Ala Gly Cys Ala Gly Ala Gly Ala Ala Gly Gly Ala Gly Cys Thr Thr Gly Gly Ala Gly 50 ~ 55 60 Cys Gly Gly Gly Cys Cys Ala Gly Gly Ala Cys Ala Gly Ala Gly Gly Ala Cys Thr Ala Thr Cys Thr Cys Ala Ala Ala Cys Gly Gly Ala Ala Gly Ala Thr Thr Cys Gly Thr Thr Cys Cys Cys Gly Gly Cys Cys Gly Gly Ala Gly Ala Gly Ala Thr Cys Gly Gly Ala Gly Cys Thr Gly Gly Thr Cys Ala Gly Gly Ala Thr Gly Cys Ala Cys Ala Thr Thr Thr Thr Gly Gly Ala Ala Gly Ala Gly Ala Cys Cys Thr Cys Gly Gly Cys Thr Gly Ala Gly Cys Cys Ala Thr Cys Cys Cys Thr~Cys Cys Ala Gly Gly Cys Cys Ala Ala Gly Cys Ala Gly Cys Thr Gly Ala Ala Gly Cys Thr Gly Ala Ala Gly Ala Gly Ala Gly Cys Cys Ala Gly Ala Cys Thr Ala Gly Cys Cys Gly Ala Thr Gly Ala Cys Cys Thr Cys Ala Ala Thr Gly Ala Gly Ala Ala Gly Ala Thr Thr Gly Cys Ala Cys Ala Gly Ala Gly Gly Cys Cys Thr Gly Gly Cys Cys Cys Cys Ala Thr Gly Gly Ala Gly Cys Thr Gly Gly Thr Gly Gly Ala Gly Ala Ala Gly Ala Ala Cys Ala Thr Cys Cys Thr Thr Cys Cys Thr Gly Thr Thr Gly Ala Gly Thr Cys Cys Ala Gly Cys Cys Thr Gly Ala Ala Gly Gly Ala Ala Gly Cys Cys Ala Thr Cys Ala Thr Thr Gly Thr Gly Gly Gly Cys Cys Ala Gly Gly Thr Gly Ala Ala Cys Thr Ala Thr Cys Cys Cys Ala Ala Ala Gly Thr Ala Gly Cys A.la Gly Ala Cys Ala Gly Cys Thr Cys Thr Thr Cys Cys .Thr Thr Cys Gly Ala Thr Gly Ala Gly Gly Ala Cys Ala Gly Cys Ala Gly Cys Gly Ala Thr Gly Cys Cys Thr Thr Ala Thr Cys Cys Cys Cys Cys Gly Ala Gly Cys Ala Gly Cys Cys Thr Gly Cys Cys Ala Gly Cys Cys Ala Thr Gly Ala Gly Thr Cys Cys Cys Ala Gly Gly Gly Thr Thr Cys Thr Gly Thr Gly Cys Cys Gly Thr Cys Ala Cys Cys Cys Cys Thr Gly Gly Ala Gly Gly Cys Cys Cys Gly Ala Gly Thr Cys Ala Gly Cys Gly Ala Ala Cys Cys Ala Cys Thr Gly Cys Thr Cys Ala Gly Thr Gly Cys Cys Ala Cys Cys Thr Cys Thr Gly Cys Ala Thr Cys Cys Cys Cys Cys Ala Cys Cys Cys Ala Gly Gly Thr 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Ala Gly Cys Thr Gly Thr Gly Thr Gly Cys Cys Ala Cys Ala Gly Thr Cys Thr Gly Gly Thr Gly Cys Cys Cys Ala Gly Thr Cys Thr Gly Gly Cys Ala Thr Gly Cys Ala Gly Cys Thr Ala Cys Cys Cys Ala Gly Gly Cys Cys Cys Ala Cys Cys Cys Ala Thr Cys Ala Cys Gly Thr Gly Thr Gly Ala Thr Thr Gly Ala Cys Ala Thr Gly Thr Ala Gly Gly Thr Ala Cys Cys Cys Thr Gly Cys Cys Ala Cys Gly Gly Cys Cys Thr Ala Thr Gly Cys Cys Cys Cys Ala Cys Cys Thr Gly Cys Cys Cys Thr Gly Cys Thr Thr Cys Cys Thr Gly Gly Cys Thr Cys Cys Thr Thr Ala Thr Cys Ala Gly Thr Gly Cys Cys Ala Thr Gly Ala Gly Gly Gly Cys Ala Gly Ala Gly Gly Thr Gly Cys Thr Ala Cys Cys Thr Gly Gly Cys Cys Thr Thr Cys Cys Thr Gly Cys Cys Ala Gly Gly Ala Gly Cys Thr Cys Thr Cys Cys Ala Cys Cys Cys Ala Cys Thr Cys Ala Cys Ala Thr Thr Cys Cys Gly Thr Cys Cys Cys Cys Gly Cys Cys Gly Cys Cys Thr Cys Ala Cys Thr Gly Cys Ala Gly Cys Cys Ala Gly Cys Gly Thr Gly Gly Thr Cys Cys Thr Ala Gly Gly Ala Cys Ala Gly Gly Ala Gly Gly Ala Gly Cys Thr Thr Cys Gly Gly Gly Cys Cys Cys Ala Gly Cys Thr Thr Cys Ala Cys Cys Cys Thr Gly Cys Gly Gly Thr Gly Gly Gly Gly Cys Thr Gly Ala Gly Gly Gly Gly Thr Gly Gly Cys Cys Ala Thr Cys Thr Cys Cys Thr Gly Cys Cys Cys Thr Gly Gly Gly Gly Cys Cys Ala Cys Thr Gly Gly Cys Thr Thr Cys Ala Cys Ala Thr Thr Cys Thr Gly Gly Gly Cys Thr Gly Ala Cys Thr Cys Ala Thr Ala Gly Gly Gly Gly Ala Gly Thr Ala Gly Gly Gly Gly Thr Gly Gly Ala Gly Thr Cys Ala Cys Cys Ala Ala Ala Ala Cys Cys Ala Gly Thr Gly Cys Thr Gly Gly Gly Ala Cys Ala Ala Ala Gly Ala Thr Gly Gly Gly Gly Ala Ala Gly Gly Thr Gly Thr Gly Thr Gly Ala Ala Cys Thr Thr Thr Thr Thr Ala Ala Ala Ala Thr Ala Ala Ala Cys Ala Cys Ala Ala Ala Ala Ala Cys Ala Cys Ala Gly <210> 25 <211> 2424 <212> DNA
<213> Homo Sapiens <220>
<221> CDS
<222> (1)..(2421) <400> 25 atg gat tct tcc gtg aaa gag get ata aaa ggt act gag gtg agc ctc 48 Met Asp Ser Ser Val Lys Glu Ala Ile Lys Gly Thr Glu Val Ser Leu tcc aag gca g,ca gat gca ttc gcc ttt gag gat gac agc agt aga gat 96 Ser Lys Ala Ala Asp Ala Phe Ala Phe Glu Asp Asp Ser Ser Arg Asp ggg ctc tct cca gat cag get agg agc gag gac ccc cag ggc tct aca 144 Gly Leu Ser Pro Asp Gln Ala Arg Ser Glu Asp Pro Gln Gly Ser Thr gga tcc acc cca gac atc aaa tcc act gag get cct ctg gac aca atc 192 Gly Ser Thr Pro Asp Ile Lys Ser Thr Glu Ala Pro Leu Asp Thr Ile.

cag gat ctc act cct ggc tca gaa agt gac aag aat gat gca gcc tcc 240 Gln Asp Leu Thr Pro Gly Ser Glu Ser Asp Lys Asn Asp Ala Ala Ser cag cca ggc aac cag tca gac cct ggg aag cag gtt ctc ggc ccc ctc 288 Gln Pro Gly Asn Gln Ser Asp Pro Gly Lys Gln Val Leu Gly Pro Leu agc acc ccg att cct gtg cac act get gta aag tcc aag tct ttg ggt 336 Ser Thr Pro Ile Pro Val His Thr Ala Val Lys Ser Lys Ser Leu Gly gac agt aag aac cgc cac aaa aag ccc aaa gac ccc aaa cca aag gtg 384 Asp Ser Lys Asn Arg His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val aag aag ctc aaa tac cat cag tac atc ccc cca gac cag aag gca gag 432 Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu aac tct ccc cca ccc atg gac tct gcc tat gcc cgg ctc ctc cag caa 480 Asn Ser Pro Pro Pro Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln cag cag cta ttc ctg cag cta cag atc ctc agc cag cag cag caa cag 528 Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln cag cag caa cag cag cag cag caa cag cag cag cag cag cag cag cag 576 Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln cgg ttc agc tac cct ggg atg cac caa aca cac ctc aaa gaa cca aat 624 Arg Phe Ser Tyr Pro Gly Met His Gln Thr His Leu Lys Glu Pro Asn gaa cag atg gcc aga aat ccg aat cct tct tca aca cca ctg agc aat 672 Glu Gln Met Ala Arg Asn Pro Asn Pro Ser Ser Thr Pro Leu Ser Asn acc cct cta tcc cct gtc aaa aat agv att tct gga caa act ggt gtt 720 Thr Pro Leu Ser Pro Val Lys Asn Xaa Ile Ser Gly Gln Thr Gly Val tct tct ctc aaa cca ggc ccc ctc cca ccc aac ctg gat gat ctc aag 768 Ser Ser Leu Lys Pro Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys gtg tca gag tta aga caa cag ctt cga atc cgg ggc ttg cca gtg tca 816 Val Ser Glu Leu Arg Gln Gln Leu Arg Ile Arg Gly Leu Pro Val Ser ggc acc aag aca gcg ctg gtg gac cgg ctt cgt ccc ttc cag gat tgt 864 Gly Thr Lys Thr Ala Leu Val Asp Arg Leu Arg Pro Phe Gln Asp Cys get ggc aac cct gtg ccc aac ttt ggg gac atc aca act gtc acc ttt 912 Ala Gly Asn Pro Val Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe cct gtc acg ccc aac acc ttg ccc agt tat cag tcc tcc ccg aca ggc 960 Pro Val Thr Pro Asn Thr Leu Pro Ser Tyr Gln Ser Ser Pro Thr Gly ttc tac cac ttt ggc agc aca agc tcc agc cca ccc atc tcc ccc gcc 1008 Phe Tyr His Phe Gly Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala tca tct gac ttg tcc get gca ggg tcc ctg cca gac acc ttc acc gat 1056 Ser Ser Asp Leu Ser Ala Ala Gly Ser Leu Pro Asp Thr Phe Thr Asp gcg tca cct ggc ttc ggc ctg cac gca tct ccg gtg ccc gcc tgc acg 1104 Ala Ser Pro Gly Phe Gly Leu His Ala Ser Pro Val Pro Ala Cys Thr gac gag agt ctg ctg agc agc ctg aat ggg ggc tcg ggc ccc tcc gag 1152 Asp Glu Ser Leu Leu Ser Ser Leu Asn Gly Gly Ser Gly Pro Ser Glu cct gat ggg cta gac tct gag aag gac aag atg ctg gtg gag aag cag 1200 Pro Asp Gly Leu Asp Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln aaa gtg atc aac cag ctc acc tgg aag ctg cgg caa gag cag cgg cag 1248 Lys Val Ile Asn Gln Leu Thr Trp Lys Leu Arg Gln Glu Gln Arg Gln gtg gaa gag ctg aga atg caa ctg cag aag cag aag agc agc tgc agc 1296 Val Glu Glu Leu Arg Met Gln Leu Gln Lys Gln Lys Ser Ser Cys Ser gac cag aag cca ctc ccc ttc ttg gcc acc acc atc aaa cag gaa gat 1344 Asp Gln Lys Pro Leu Pro Phe Leu Ala Thr Thr Ile Lys Gln Glu Asp gtc tcc agc tgc ccc ttc gca ccc cag cag gcg tct ggg aag gga cag 1392 Val Ser-Ser Cys Pro Phe Ala Pro Gln Gln Ala Ser Gly Lys Gly Gln ggc cac agc tct gac agt ccc cct ccg get tgt gag acg get cag ctg 1440 Gly His Ser Ser Asp Ser Pro Pro Pro Ala Cys Glu Thr Ala Gln Leu ctg cct cac tgt gtg gag tcc tca ggt caa acc cat gta ctc tcg tcc 1488 Leu Pro His Cys Val Glu Ser Ser Gly Gln Thr His Val Leu Ser Ser acg ttt ctc agc ccc cag tgc tcc cct cag cac tcg ccc cgt ggg ggc 1536 Thr Phe Leu Ser Pro Gln Cys Ser Pro Gln His Ser Pro Arg Gly Gly ctg aag agc ccg cag cac atc agc ctg cct cca tca ccc aac aac cat 1584 Leu Lys Ser Pro Gln His Ile Ser Leu Pro Pro Ser Pro Asn Asn His tac ttc ctg get tcc tct tcg gga get cag aga gag aac cat ggg gtc 1632 Tyr Phe Leu Ala Ser Ser Ser Gly Ala Gln Arg Glu Asn His Gly Val tct tca ccc agc agc agc caa ggg tgc gca cag atg act ggt tta caa 1680 Ser Ser Pro Ser Ser Ser Gln Gly Cys Ala Gln Met Thr Gly Leu Gln 545 550 555' 560 tct tct gac aag gtg ggg cca acg ttt tca att cca tcc cca act ttt 1728 Ser Ser Asp Lys Val Gly Pro Thr Phe Ser Ile Pro Ser Pro Thr Phe tct aag tca agt tca gca gtt tca gat atc acc cag ccc cca tcc tat 1776 Ser Lys Ser Ser Ser Ala Val Ser Asp Ile Thr Gln Pro Pro Ser Tyr gaa gat gca gtg aag cag caa atg act cgg agt cag cag atg gac gaa 1824 Glu Asp Ala Val Lys Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu ctc ctg gat gtc ctc att gaa agt gga gaa atg cca gcc gat gcc agg 1872 Leu Leu Asp Val Leu Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg gaa gat cat tca tgt ctt cag aaa att cca aag atc cct ggg tcc tcc 1920 Glu Asp His Ser Cys Leu Gln Lys Ile Pro Lys Ile Pro Gly Ser Ser tgc agc cca act gcc atc ccc ccg aag ccc tcg get tcc ttt gag cag 1968 Cys Ser Pro Thr Ala Ile Pro Pro Lys Pro Ser Ala Ser Phe Glu Gln gca tct tcg gga ggc cag atg gcc ttc gat cac tac gca aac gac agt 2016 Ala Ser Ser Gly Gly Gln Met Ala Phe Asp His Tyr Ala Asn Asp Ser gac gaa cac ctg gaa gtc tta ttg aat tct cac agc ccc atc gga aag 2064 Asp Glu His Leu Glu Val Leu Leu Asn Ser His Ser Pro Ile Gly Lys gtg agc gat gtt acc ctc ctc aaa atc gga agc gag gag cct cct ttt 2112 Val Ser Asp Val Thr Leu Leu Lys Ile Gly Ser Glu Glu Pro Pro Phe gac agc atc atg gat ggc ttc cca ggg aag get gcg gaa gat ctc ttc 2160 Asp Ser Ile Met Asp Gly Phe Pro Gly Lys Ala Ala Glu Asp Leu Phe agt get cac gag ctc ttg cct ggg ccc ctc tcc ccg atg cat gca cag 2208 Ser Ala His Glu Leu Leu Pro Gly Pro Leu Ser Pro Met His Ala Gln ttg tca cct cct tct gtg gac agc agt ggt ctg cag ctg agc tta ccg 2256 Leu Ser Pro Pro Ser Val Asp Ser Ser Gly Leu Gln Leu Ser Leu Pro gaa tct cct tgg gaa aca atg gaa tgg ctg gac ctc act cca cct agt 2304 Glu Ser Pro Trp Glu Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Ser tcc acg cca ggc ttc agc aac ctt acc tcc agt ggg ccc agc att ttc 2352 Ser Thr Pro Gly Phe Ser Asn Leu Thr Ser Ser Gly Pro Ser Ile Phe aac atc gat ttt ctg gat gtt aca gat ctt aat ctg aat tcc cct atg 2400 Asn Ile Asp Phe Leu Asp Val Thr Asp Leu Asn Leu Asn Ser Pro Met gat ctc cac tta cag cag tgg taa 2424 Asp Leu His Leu Gln Gln Trp <210> 26 <211> 807 <212> PRT
<213> Homo sapiens <400> 26 Met Asp Ser Ser Val Lys Glu Ala Ile Lys Gly Thr Glu Val Ser Leu Ser Lys Ala Ala Asp Ala Phe Ala Phe Glu Asp Asp Ser Ser Arg Asp Gly Leu Ser Pro Asp Gln Ala Arg Ser Glu Asp Pro Gln Gly Ser Thr Gly Ser Thr Pro Asp Ile Lys Ser Thr Glu Ala Pro Leu Asp Thr Ile Gln Asp Leu Thr Pro Gly Ser Glu Ser Asp Lys Asn Asp Ala Ala Ser Gln Pro Gly Asn Gln Ser Asp Pro Gly Lys Gln Val Leu Gly Pro Leu Ser Thr Pro Ile Pro Val His Thr Ala Val Lys Ser Lys Ser Leu Gly Asp Ser Lys Asn Arg His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu Asn Ser Pro Pro Pro Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Arg Phe Ser Tyr Pro Gly Met His Gln Thr His Leu Lys Glu Pro Asn Glu Gln Met Ala Arg Asn Pro Asn Pro Ser Ser Thr Pro Leu Ser Asn Thr Pro Leu Ser Pro Val Lys Asn Xaa Ile Ser Gly Gln Thr Gly Val Ser Ser Leu Lys Pro Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys Val Ser Glu Leu Arg Gln Gln Leu Arg Ile Arg Gly Leu Pro Val Ser Gly Thr Lys Thr Ala Leu Val Asp Arg Leu Arg Pro Phe Gln Asp Cys Ala Gly Asn Pro Val Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe Pro Val Thr Pro Asn Thr Leu Pro Ser Tyr Gln Ser Ser Pro Thr Gly Phe Tyr His Phe Gly Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala Ser Ser Asp Leu Ser Ala Ala Gly Ser Leu Pro Asp Thr Phe Thr Asp Ala Ser Pro Gly Phe Gly Leu His Ala Ser Pro Val Pro Ala Cys Thr Asp Glu Ser Leu Leu Ser Ser Leu Asn Gly Gly Ser Gly Pro Ser Glu Pro Asp Gly Leu Asp Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln Lys Val Ile Asn Gln Leu Thr Trp Lys Leu Arg Gln Glu Gln Arg Gln Val Glu Glu Leu Arg Met Gln Leu Gln Lys Gln Lys Ser Ser Cys Ser Asp Gln Lys Pro Leu Pro Phe Leu Ala Thr Thr Ile Lys Gln Glu Asp Val Ser Ser Cys Pro Phe Ala Pro Gln Gln Ala Ser Gly Lys Gly Gln Gly His Ser Ser Asp Ser Pro Pro Pro Ala Cys Glu Thr Ala Gln Leu Leu Pro His Cys Val Glu Ser Ser Gly Gln Thr His Val Leu Ser Ser Thr Phe Leu Ser Pro Gln Cys Ser Pro Gln His Ser Pro Arg Gly Gly Leu Lys Ser Pro Gln His Ile Ser Leu Pro Pro Ser Pro Asn Asn His Tyr Phe Leu Ala Ser Ser Ser Gly Ala Gln Arg Glu Asn His Gly Val Ser Ser Pro Ser Ser Ser Gln Gly Cys Ala Gln Met Thr Gly Leu Gln Ser Ser Asp Lys Val Gly Pro Thr Phe Ser Ile Pro Ser Pro Thr Phe Ser Lys Ser Ser Ser Ala Val Ser Asp Ile Thr Gln Pro Pro Ser Tyr Glu Asp Ala Val Lys Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu Leu Leu Asp Val Leu Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg Glu Asp His Ser Cys Leu Gln Lys Ile Pro Lys Ile Pro Gly Ser Ser Cys Ser Pro Thr Ala Ile Pro Pro Lys Pro Ser Ala Ser Phe Glu Gln Ala Ser Ser Gly Gly Gln Met Ala Phe Asp His Tyr Ala Asn Asp Ser Asp Glu His Leu Glu Val Leu Leu Asn Ser His Ser Pro Ile Gly Lys Val Ser Asp Val Thr Leu Leu Lys Ile Gly Ser Glu Glu Pro Pro Phe Asp Ser Ile Met Asp Gly Phe Pro Gly,Lys Ala Ala Glu Asp Leu Phe Ser Ala His Glu Leu Leu Pro Gly Pro Leu Ser Pro Met His Ala Gln Leu Ser Pro Pro Ser Val Asp Ser Ser Gly Leu Gln Leu Ser Leu Pro Glu Ser Pro Trp Glu Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Ser Ser Thr Pro Gly Phe Ser Asn Leu Thr Ser Ser Gly Pro Ser Ile Phe Asn Ile Asp Phe Leu Asp Val Thr Asp Leu Asn Leu Asn Ser Pro Met Asp Leu His Leu Gln Gln Trp <210> 27 <211> 3063 <212> DNA
<213> Homo sapiens <400> 27 gacgtcgcat gctcccggcc gccatggcgg ccgcgggaat tcgattgact cctggagccc 60 gtcagtatcg gcggaattcg cggccgcgtc gacctggctg ccactgtact cctacccagg 120 ggagctcacg gagagttgga tgaattctgg gttgttagct gcggtcagct gggctcccgg 180 gagcctgttg ctggtggaga acagggggcg cctggccaag ggaccagcgg cttgctgaga 240 ctcaacatga cactcctggg gtctgagcat tccttgctga ttaggagcaa gttcagatca 300 gttttacagt taagacttca acaaagaagg acccaggaac aactggctaa ccaaggcata 360 ataccaccac tgaaacgtcc agctgaattc catgagcaaa gaaaacattt ggatagtgac 420 aaggctaaaa attccctgaa gcgcaaagcc agaaacaggt gcaacagtgc cgacttggtt 480 aatatgcaca tactccaagc ttccactgca gagaggtcca ttccaactgc tcagatgaag 540 ctgaaaagag cccgactcgc cgatgatctc aatgaaaaaa ttgctctacg accagggcca 600 ctggagctgg tggaaaaaaa cattcttcct gtggattctg ctgtgaaaga ggccataaaa 660 ggtaaccagg tgagtttctc caaatccacg gatgcttttg cctttgaaga ggacagcagc 720 agcgatgggc tttctccgga tcagactcga agtgaagacc cccaaaactc agcgggatcc 780 ccgccagacg ctaaagcctc agatacccct tcgacaggtt ctctggggac aaaccaggat 840 cttgcttctg gctcagaaaa tgacagaaat gactcagcct cacagcccag ccaccagtca 900 gatgcgggga agcaggggct tggccccccc agcaccccca tagccgtgca tgctgctgta 960 aagtccaaat ccttgggtga cagtaagaac cgccacaaaa agcccaagga ccccaagcca 1020 aaggtgaaga agcttaaata tcaccagtac attcccccag accagaaggc agagaagtcc 1080 cctccaccta tggactcagc ctacgctcgg ctgctccagc aacagcagct gttcctgcag 1140 ctccaaatcc tcagccagca gcagcagcag cagcaacacc gattcagcta cctagggatg 1200 caccaagctc agcttaagga accaaatgaa cagatggtca gaaatccaaa ctcttcttca 1260 acgccactga gcaatacccc cttgtctcct gtcaaaaaca gtttttctgg acaaactggt 1320 gtctcttctt tcaaaccagg cccactccca cctaacctgg atgatctgaa ggtctctgaa 1380 ttaagacaac agcttcgaat tcggggcttg cctgtgtcag gcaccaaaac ggctctcatg 1440 gaccggcttc gacccttcca ggactgctct ggcaacccag tgccgaactt tggggatata 1500 acgactgtca cttttcctgt cacacccaac acgctgccca attaccagtc ttcctcttct 1560 accagtgccc tgtccaacgg cttctaccac tttggcagca ccagctccag ccccccgatc 1620 tccccagcct cctctgacct gtcagtcgct gggtccctgc cggacacctt caatgatgcc 1680 tccccctcct tcggcctgca cccgtcccca gtccacgtgt gcacggagga aagtctcatg 1740 agcagcctga atgggggctc tgttccttct gagctggatg ggctggactc cgagaaggac 1800 aagatgctgg tggagaagca gaaggtgatc aatgaactca cctggaaact ccagcaagag 1860 cagaggcagg tggaggagct gaggatgcag cttcagaagc agaaaaggaa taactgttca 1920 gagaagaagc cgctgccttt cctggctgcc tccatcaagc aggaagaggc tgtctccagc 1980 tgtccttttg catcccaagt acctgtgaaa agacaaagca gcagctcaga gtgtcaccca 2040 ccggcttgtg aagctgctca actccagcct cttggaaatg ctcattgtgt ggagtcctca 2100 gatcaaacca atgtactttc ttccacattt ctcagccccc agtgttcccc tcagcattca 2160 ccgctggggg ctgtgaaaag cccacagcac atcagtttgc ccccatcacc caacaaccct 2220 cactttctgc cctcatcctc cggggcccag ggagaagggc acagggtctc ctcgcccatc 2280 agcagccagg tgtgcactgc acagatggct ggtttacact cttctgataa ggtggggcca 2340 aagttttcaa ttccatcccc aactttttct aagtcaagtt cagcaatttc agaggtaaca 2400 cagcctccat cctatgaaga tgccgtaaag cagcaaatga cccggagtca gcagatggat 2460 gaactcctgg acgtgcttat tgaaagcgga gaaatgccag cagacgctag agaggatcac 2520 tcatgtcttc aaaaagtccc aaagataccc agatcttccc gaagtccaac tgctgtcctc 2580 accaagccct cggcttcctt tgaacaagcc tcttcaggca gccagatccc ctttgatccc 2640 tatgccaccg acagtgatga gcatcttgaa gtcttattaa attcccagag ccccctagga 2700 aagatgagtg atgtcaccct tctaaaaatt gggagcgaag agcctcactt tgatgggata 2760 atggatggat tctctgggaa ggctgcagaa gacctcttca atgcacatga gatcttgcca 2820 ggccccctct ctccaatgca gacacagttt tcaccctctt ctgtggacag caatgggctg 2880 cagttaagct tcactgaatc tccctgggaa accatggagt ggctggacct cactccgcca 2940 aattccacac caggctttag cgccctcacc accagcagcc ccagcatctt caacatcgat 3000 ttcctggatg tcactgatct caatttgaat tcttccatgg accttcactt gcagcagtgg 3060 tag 3063 <210> 28 <211> 938 <212> PRT
<213> Homo Sapiens <400> 28 Met Thr Leu Leu Gly Ser Glu His Ser Leu Leu Ile Arg Ser Lys Phe Arg Ser Val Leu Gln Leu Arg Leu Gln Gln Arg Arg Thr Gln Glu Gln Leu Ala Asn Gln Gly Ile Ile Pro Pro Leu Lys Arg Pro Ala Glu Phe His Glu Gln Arg Lys His Leu Asp Ser Asp Lys Ala Lys Asn Ser Leu Lys Arg Lys Ala Arg Asn Arg Cys Asn Ser Ala Asp Leu Val Asn Met His Ile Leu Gln Ala Ser Thr Ala Glu Arg Ser Ile Pro Thr Ala Gln Met Lys Leu Lys Arg Ala Arg Leu Ala Asp Asp Leu Asn Glu Lys Ile Ala Leu Arg,Pro Gly Pro Leu Glu Leu Val Glu Lys Asn Ile Leu Pro Val Asp Ser Ala Val Lys Glu Ala Ile Lys Gly Asn Gln Val Ser Phe Ser Lys Ser Thr Asp Ala Phe Ala Phe Glu Glu Asp Ser Ser Ser Asp Gly Leu Ser Pro Asp Gln Thr Arg Ser Glu Asp Pro Gln Asn Ser Ala Gly Ser Pro Pro Asp Ala Lys Ala Ser Asp Thr Pro Ser Thr Gly Ser Leu Gly Thr Asn Gln Asp Leu Ala Ser Gly Ser Glu Asn Asp Arg Asn Asp Ser Ala Ser Gln Pro Ser His Gln Ser Asp Ala Gly Lys Gln Gly Leu Gly Pro Pro Ser Thr Pro Ile Ala Val His Ala Ala Val Lys Ser Lys Ser Leu Gly Asp Ser Lys Asn Arg His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu Lys Ser Pro Pro Pro Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln Gln Gln His Arg Phe Ser Tyr Leu Gly Met His Gln Ala Gln Leu Lys Glu Pro Asn Glu Gln Met Val Arg Asn Pro Asn Ser Ser Ser Thr Pro Leu Ser Asn Thr Pro Leu Ser Pro Val Lys Asn Ser Phe Ser Gly Gln Thr Gly Val Ser Ser Phe Lys Pro Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys Val Ser Glu Leu Arg Gln Gln Leu Arg $~

Ile Arg Gly Leu Pro Val Ser Gly Thr Lys Thr Ala Leu Met Asp Arg Leu Arg Pro Phe Gln Asp Cys Ser Gly Asn Pro Val Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe Pro Val Thr Pro Asn Thr Leu Pro Asn Tyr Gln Ser Ser Ser Ser Thr Ser Ala Leu Ser Asn Gly Phe Tyr His Phe Gly Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala Ser Ser Asp Leu Ser Val Ala Gly Ser Leu Pro Asp Thr Phe Asn Asp Ala Ser Pro Ser Phe Gly Leu His Pro Ser Pro Val His Val Cys Thr Glu Glu Ser Leu Met Ser Ser Leu Asn Gly Gly Ser Val Pro Ser Glu Leu Asp Gly Leu Asp Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln Lys Val Ile Asn Glu Leu Thr Trp Lys Leu Gln Gln Glu Gln Arg Gln Val Glu Glu Leu Arg Met Gln Leu Gln Lys Gln Lys Arg Asn Asn Cys Ser Glu Lys Lys Pro Leu Pro Phe Leu Ala Ala Ser Ile Lys Gln Glu Glu Ala Val Ser Ser Cys Pro Phe Ala Ser Gln Val Pro Val Lys Arg Gln Ser Ser Ser Ser Glu Cys His Pro Pro Ala Cys Glu Ala Ala Gln Leu Gln Pro Leu Gly Asn Ala His Cys Val Glu Ser Ser Asp Gln Thr Asn Val Leu Ser Ser Thr Phe Leu Ser Pro Gln Cys Ser Pro Gln His Ser Pro Leu Gly Ala Val Lys Ser Pro Gln His Ile Ser Leu Pro Pro Ser Pro Asn Asn Pro His Phe Leu Pro Ser Ser Ser Gly Ala Gln Gly Glu Gly His $1 Arg Val Ser Ser Pro Ile Ser Ser Gln Val Cys Thr Ala Gln Met Ala Gly Leu His Ser Ser Asp Lys Val Gly Pro Lys Phe Ser Ile Pro Ser Pro Thr Phe Ser Lys Ser Ser Ser Ala Ile Ser Glu Val Thr Gln Pro Pro Ser Tyr Glu Asp Ala Val Lys Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu Leu Leu Asp Val Leu Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg Glu Asp His Ser Cys Leu Gln Lys Val Pro Lys Ile Pro Arg Ser Ser Arg Ser Pro Thr Ala Val Leu Thr Lys Pro Ser Ala Ser Phe Glu Gln Ala Ser Ser Gly Ser Gln Ile Pro Phe Asp Pro Tyr Ala 785' 790 795 800 Thr Asp Ser Asp Glu His Leu Glu Val Leu Leu Asn Ser Gln Ser Pro Leu Gly Lys Met Ser Asp Val Thr Leu Leu Lys Ile Gly Ser Glu Glu Pro His Phe Asp Gly Ile Met Asp Gly Phe Ser Gly Lys Ala Ala Glu Asp Leu Phe Asn Ala His Glu Ile Leu Pro Gly Pro Leu Ser Pro Met Gln Thr Gln Phe Ser Pro Ser Ser Val Asp Ser Asn Gly Leu Gln Leu Ser Phe Thr Glu Ser Pro Trp Glu Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Asn Ser Thr Pro Gly Phe Ser Ala Leu Thr Thr Ser Ser Pro Ser Ile Phe Asn Ile Asp Phe Leu Asp Val Thr Asp Leu Asn Leu Asn Ser Ser Met Asp Leu His Leu Gln Gln Trp <210> 29 <211> 4960 <212> DNA

<213> Mus musculus <400> 29 ggaattcggc acgaggccac cctcagagga ggagggtcct gcctgctggg agttaattag 60 cctcgcgagc ggcgaggggg gaggcgccag ttttctgggg acactggcgg ccactgtgcg 120 tcctcctacc caagggagct ccccaagagt tggatgaatt ctgggttgtt agctgctgtc 180 ctctgggctc ccgggagcca gtttctggtg gaaagcgggg cgcctggcca acgaccagcg 240 gcttgctgag actcaccatg acactcctgg ggtctgaaca ctctttgctg attagaagga 300 agttccgatc agtcttacag ttacggcttc aacagagaag gacccaggag cagctggcta 360 accaaggctt aataccgcca ctgaaaggtc caactgaatt ccatgacccg agaaaacaat 420 tggatagtgc caagactgaa gattccctga ggcgcaaggg cagaaacagg tccgaccgtg 480 ccagcctggt tactatgcac attctccaag cctccacggc agaaaggtcc attccaactg 540 ctcagatgaa gctcaaaaga gcccgccttg cagatgacct caatgagaag atcgctctcc 600 gccaagggcc cttggaactg gtggagaaga acattctgcc gatggattct tccgtgaaag 660 aggctataaa aggtactgag gtgagcctct ccaaggcagc agatgcattc gcctttgagg 720 atgacagcag tagagatggg ctctctccag atcaggctag gagcgaggac ccccagggct 780 ctacaggatc caccccagac atcaaatcca ctgaggctcc tctggacaca atccaggatc 840 tcactcctgg ctcagaaagt gacaagaatg atgcagcctc ccagccaggc aaccagtcag 900 accctgggaa gcaggttctc ggccccctca gcaccccgat tcctgtgcac actgctgtaa 960 agtccaagtc tttgggtgac agtaagaacc gccacaaaaa gcccaaagac cccaaaccaa 1020 aggtgaagaa gctcaaatac catcagtaca tccccccaga ccagaaggca gagaagtctc 1080 ccccacccat ggactctgcc tatgcccggc tgctccagca acagcagcta ttcctgcagc 1140 tacagatcct cagccagcag cagcaacagc agcagcaaca gcagcagcag caacagcagc 1200 agcagcagca gcagcagcgg ttcagctacc ctgggatgca ccaaacacac ctcaaagaac 1260 caaatgaaca gatggccaga aatccgaatc cttcttcaac accactgagc aatacccctc 1320 tatcccctgt caaaaatagc atttctggac aaactggtgt ttcttctctc aaaccaggcc 1380 ccctcccacc caacctggat gatctcaagg tgtcagagtt aagacaacag cttcgaatcc 1440 ggggcttgcc agtgtcaggc accaagacag cgctggtgga ccggcttcgt cccttccagg 1500 attgtgctgg caaccctgtg cccaactttg gggacatcac aactgtcacc tttcctgtca 1560 cgcccaacac cttgcccagt tatcagtcct ccccgacagg cttctaccac tttggcagca 1620 caagctccag cccacccatc tcccccgcct catctgactt gtccgctgca gggtccctgc 1680 cagacacctt caccgatgcg tcacctggct tcggcctgca cgcatctccg gtgcccgcct 1740 gcacggacga gagtctgctg agcagcctga atgggggctc gggcccctcc gagcctgatg 1800 ggctagactc tgagaaggac aagatgctgg tggagaagca gaaagtgatc aaccagctca 1860 cctggaagct gcggcaagag cagcggcagg tggaagagct gagaatgcaa ctgcagaagc 1920 agaagagcag ctgcagcgac cagaagccac tgcccttctt ggccaccacc atcaaacagg 1980 aagatgtctc cagctgcccc ttcgcacccc agcaggcgtc tgggaaggga cagggccaca 2040 gctctgacag tccccctccg gcttgtgaga cggctcagct gctgcctcac tgtgtggagt 2100 cctcaggtca aacccatgta ctctcgtcca cgtttctcag cccccagtgc tcccctcagc 2160 actcgcccct ggggggcctg aagagcccgc agcacatcag cctgcctcca tcacccaaca 2220 accattactt cctggcttcc tcttcgggag ctcagagaga gaaccatggg gtctcttcac 2280 ccagcagcag ccaagggtgc gcacagatga ctggtttaca atcttctgac aaggtggggc 2340 caacgttttc aattccatcc ccaacttttt ctaagtcaag ttcagcagtt tcagatatca 2400 cccagccccc atcctatgaa gatgcagtga agcagcaaat gactcggagt cagcagatgg 2460 acgaactcct ggatgtcctc attgaaagtg gagaaatgcc agccgatgcc agggaagatc 2520 attcatgtct tcagaaaatt ccaaagatcc ctgggtcctc ctgcagccca actgccatcc 2580 ccccgaagcc ctcggcttcc tttgagcagg catcttcggg aggccagatg gccttcgatc 2640 actacgccaa cgacagtgac gaacacctgg aagtcttatt gaattctcac agccccatcg 2700 gaaaggtgag cgatgttacc ctcctcaaaa tcggaagcga ggagcctcct tttgacagca 2760 tcatggatgg cttcccaggg aaggctgcgg aagatctctt cagtgctcac gagctcttgc 2820 ctgggcccct ctccccgatg catgcacagt tgtcacctcc ttctgtggac agcagtggtc 2880 tgcagctgag cttcacggaa tctccttggg aaacaatgga atggctggac ctcactccac 2940 ctagttccac gccaggcttc agcaacctta cctccagtgg gcccagcatt ttcaacatcg 3000 attttctgga tgttacagat cttaatctga attcccctat ggatctccac ttacagcagt 3060 ggtaaacacc cgaggtacaa gagctacgag agctcagtgg gaattcaatg gaggaaagca 3120 cgataccgga aatgtgtgtt ccaaaagatg aaggggggaa aatggggagg gaaaaaaaaa 3180 aacagcaacg gaggtttttg tgacaactaa ccagaacaaa cagaagtcag ctattaaaat 3240 atgtctaaat gtaatatcta ccagcattca gtaactgtta ataacttcag tgatgcattc 3300 aaaaatgtgc tttgtcagaa taagaatgcc aaaaatgttt tttcgctgcc ttatctcata 3360 ccagtttttt tgggtttttt tttgtttgtt tgttttttgg tttttttttt tttgtgtgtg 3420 ttgttatttg gttttctttt tgcccacagt ttgtctcagg caatactggg acataggctg 3480 accccattag cttttgttat gaatttacta aactttctgt ggaaggagaa cagagcctct 3540 gccgcgggtg tggggaagcc atcctgtgct tgaggcagca cacgtgtgtc catcatcatc 3600 agtcagaaga gcagggcctg tctcacccaa tcgagtcctt aagacagaat aatcagaatg 3660 gtcagaggga cagaccaatc aattcccagg aaagcaaaag tgactcaatg tcccttgact 3720 cccaaatggt cccactggac tggtgatcac tggtgacaac taactagctt tgtccagaga 3780 atccacccag aacacggtgc tttttagcca gtagtccacc tctatgtgca tcagcaatgc 3840 atagcaggtg agaacttgaa tcacagaaac ttcatgccat ggatggagac tcctgaggcg 3900 ctcaaatact actacctcta gttccaaaga ctagagctag atgatcagaa aggcaactgg 3960 aggcccaggg agccgtactg ggacaagtta gaattagaga acgatgtcat ttaacattcc 4020 gagaaagaaa taaccatgaa ttgctattac aggagtaaca cacagggcca gcttcttttt 4080 tcttcttttt tatttttctt ttcttattgt gagcagaggg aattcacctc agttcatctt 4140 tctctcagta cttttctttc aagatatcaa tcctttatga ctcttttgct tttaattctc 4200 tctctctctc tctctctctc tctctctctt tctctcaaag gagaggtttc agttctaaca 4260 agctaccata gtcctattaa agccattttt ttttttagaa tattaaaagt ccaaactctc 4320 ttgccaaact ctttcttcac atgcgcattg gctgaaaaca gaatttacaa gaatttcttt 4380 aggaagaaac tggggatgtg gcccattggt cacaaagttt ttttgtttgt ttttgttttt 4440 gtttcaattc ttgtttgatt tatggacaat ctttggtttg tattgctctg gagaaattgg 4500 aaatcattgc agagtgaaga taaatcaggg caccatgtat agtagagaat gtttcagtag 4560 ttttccaaac gagaacacaa ttgcacactg taaacaacag gagtgtgaag gaccacagtc 4620 ttgaggagtt cttgttgccc tgtgtttggt gaaggcgttg gggaccgagg aagacaacat 4680 acagtttggc caaggctctc agaggcttgc tgtggcgcca attcaagtat tacaatgttg 4740 catgctgtag aaagtagctg ttgctgttgt tttgttttgt tttaatttaa gtcaccaagg 4800 cactgtttta ttcttttgta aaaaaaaaaa aagttcactg tgcacttata gagaaaataa 4860 tcaacaatgt tgtgaatttt tgagaagact tttttttttt tgataaacca aagatttaga 4920 aatcattcca ttgtcaactt gtaaaaaaaa aaaaaaaaaa 4960 <210> 30 <211> 935 <212> PRT
<213> Mus musculus <400> 30 Met Thr Leu Leu Gly Ser Glu His Ser Leu Leu Ile Arg Arg Lys Phe Arg Ser Val Leu Gln Leu Arg Leu Gln Gln Arg Arg Thr Gln Glu Gln Leu Ala Asn Gln Gly Leu Ile Pro Pro Leu Lys Gly Pro Thr Glu Phe His Asp Pro Arg Lys Gln Leu Asp Ser Ala Lys Thr Glu Asp Ser Leu Arg Arg Lys Gly Arg Asn Arg Ser Asp Arg Ala Ser Leu Val Thr Met His Ile Leu Gln Ala Ser Thr Ala Glu Arg Ser Ile Pro Thr Ala Gln Met Lys Leu Lys Arg Ala Arg Leu Ala Asp Asp Leu Asn Glu Lys Ile Ala Leu Arg Gln Gly Pro Leu Glu Leu Val Glu Lys Asn Ile Leu Pro Met Asp Ser Ser Val Lys Glu Ala Ile Lys Gly Thr Glu Val Ser Leu Ser Lys Ala Ala Asp Ala Phe Ala Phe Glu Asp Asp Ser Ser Arg Asp Gly Leu Ser Pro Asp Gln Ala Arg Ser Glu Asp Pro Gln Gly Ser Thr Gly Ser Thr Pro Asp Ile Lys Ser Thr Glu Ala Pro Leu Asp Thr Ile Gln Asp Leu Thr Pro Gly Ser Glu Ser Asp Lys Asn Asp Ala Ala Ser Gln Pro Gly Asn Gln Ser Asp Pro Gly Lys Gln Val Leu Gly Pro Leu Ser Thr Pro Ile Pro Val His Thr Ala Val Lys Ser Lys Ser Leu Gly Asp Ser Lys Asn Arg His Lys Lys Pro Lys Asp Pro Lys Pro Lys Val Lys Lys Leu Lys Tyr His Gln Tyr Ile Pro Pro Asp Gln Lys Ala Glu Lys Ser Pro Pro Pro Met Asp Ser Ala Tyr Ala Arg Leu Leu Gln Gln Gln Gln Leu Phe Leu Gln Leu Gln Ile Leu Ser Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Gln Arg Phe Ser Tyr Pro Gly Met His Gln Thr His Leu Lys Glu Pro Asn Glu Gln Met Ala Arg Asn Pro Asn Pro Ser Ser Thr Pro Leu Ser Asn Thr Pro Leu Ser Pro Val Lys Asn Ser Ile Ser Gly Gln Thr Gly Val Ser Ser Leu Lys Pro Gly Pro Leu Pro Pro Asn Leu Asp Asp Leu Lys Val Ser Glu Leu Arg Gln Gln Leu Arg Ile Arg Gly Leu Pro Val Ser Gly Thr Lys Thr Ala Leu Val Asp Arg Leu Arg Pro Phe Gln Asp Cys Ala Gly Asn Pro Val Pro Asn Phe Gly Asp Ile Thr Thr Val Thr Phe Pro Val Thr Pro Asn Thr Leu Pro Ser Tyr Gln Ser Ser Pro Thr Gly Phe Tyr His Phe Gly Ser Thr Ser Ser Ser Pro Pro Ile Ser Pro Ala Ser Ser Asp Leu Ser Ala Ala Gly Ser Leu Pro Asp Thr Phe Thr Asp Ala Ser Pro Gly Phe Gly Leu His Ala Ser Pro Val Pro Ala Cys Thr Asp Glu Ser Leu Leu Ser Ser Leu Asn Gly Gly Ser Gly Pro Ser Glu Pro Asp Gly Leu Asp Ser Glu Lys Asp Lys Met Leu Val Glu Lys Gln Lys Val Ile Asn Gln Leu Thr Trp Lys Leu Arg Gln Glu Gln Arg Gln Val Glu Glu Leu Arg Met Gln Leu Gln Lys Gln Lys Ser Ser Cys Ser Asp Gln Lys Pro Leu Pro Phe Leu Ala Thr Thr Ile Lys Gln Glu Asp Val Ser Ser Cys Pro Phe Ala Pro Gln Gln Ala Ser Gly Lys Gly Gln Gly His Ser Ser Asp Ser Pro Pro Pro Ala Cys Glu Thr Ala Gln Leu Leu Pro His Cys Val Glu Ser Ser Gly Gln Thr His Val Leu Ser Ser Thr Phe Leu Ser Pro Gln Cys Ser Pro Gln His Ser Pro Leu Gly Gly Leu Lys Ser Pro Gln His Ile Ser Leu Pro Pro Ser Pro Asn Asn His Tyr Phe Leu Ala Ser Ser Ser Gly Ala Gln Arg Glu Asn His Gly Val Ser Ser Pro Ser Ser Ser=~n Gly Cys Ala Gln Met Thr Gly Leu Gln Ser Ser Asp Lys Val Gly Pro Thr Phe Ser Ile Pro Ser Pro Thr Phe Ser Lys Ser Ser Ser Ala Val Ser Asp Ile Thr Gln Pro Pro Ser Tyr Glu Asp Ala Val Lys Gln Gln Met Thr Arg Ser Gln Gln Met Asp Glu Leu Leu Asp Val Leu Ile Glu Ser Gly Glu Met Pro Ala Asp Ala Arg Glu Asp His Ser Cys Leu Gln Lys Ile Pro Lys Ile Pro Gly Ser Ser Cys Ser Pro Thr Ala Ile Pro Pro Lys Pro Ser Ala Ser Phe Glu Gln Ala Ser Ser Gly Gly Gln Met Ala Phe Asp His Tyr Ala Asn Asp Ser Asp Glu His Leu Glu Val Leu Leu Asn Ser His Ser Pro Ile Gly Lys Val Ser Asp Val Thr Leu Leu Lys Ile Gly Ser Glu Glu Pro Pro Phe Asp Ser Ile Met Asp Gly Phe Pro Gly Lys Ala Ala Glu Asp Leu Phe Ser Ala His Glu Leu Leu Pro Gly Pro Leu Ser Pro Met His Ala Gln Leu Ser Pro Pro Ser Val Asp Ser Ser Gly Leu Gln Leu Ser Phe Thr Glu Ser Pro Trp Glu Thr Met Glu Trp Leu Asp Leu Thr Pro Pro Ser Ser Thr Pro Gly Phe Ser Asn Leu Thr Ser Ser Gly Pro Ser Ile Phe Asn Ile Asp Phe Leu Asp Val Thr Asp Leu Asn Leu Asn Ser Pro Met Asp Leu His Leu Gln Gln Trp $7

Claims (126)

1. An isolated polynucleotide encoding a myocardin polypeptide.

2. The isolated polymucleotide of claim 1, wherein the myocardin polypeptide comprises an amino acid sequence of SEQ ID NO:2, SEQ ID NO:26, SEQ ID
NO:28, or SEQ ID NO:30.

3. The isolated polynucleotide of claim 2, wherein the polynucleotide sequence comprises SEQ ID NO:1, SEQ ID NO:25, SEQ ID NO:27 or SEQ ID NO:29.

4. The polynucleotide of claim 1, wherein said polynucleotide further comprises a promoter operable in eukaryotic cells.

5. An isolated nucleic acid segment comprising at least 15 contiguous nucleotides of SEQ ID NO:1, SEQ ID NO:25, SEQ ID NO:27 or SEQ ID
NO:29.

6. The isolated nucleic acid segment of claim 5, wherein said segment is 15 nucleotides in length.

7. The isolated nucleic acid segment of claim 5, wherein said segment is 20 nucleotides in length.

8. The isolated nucleic acid segment of claim 5, wherein said segment is 25 nucleotides in length.

9. The isolated nucleic acid segment of claim 5, wherein said segment is 30 nucleotides in length.

10. The isolated nucleic acid segment of claim 5, wherein said segment is 35 nucleotides in length.

11. The isolated nucleic acid segment of claim 5, wherein said segment is 50 nucleotides in length.

12. The isolated nucleic acid segment of claim 5, wherein said segment is 100 nucleotides in length.

13. The isolated nucleic acid segment of claim 5, wherein said segment is 150 nucleotides in length.

14. The isolated nucleic acid segment of claim 5, wherein said segment is 250 nucleotides in length.

15. The isolated nucleic acid segment of claim 5, wherein said segment is 500 nucleotides in length.

16. The isolated nucleic acid segment of claim 5, wherein said segment is 1000 nucleotides in length.

17. The isolated nucleic acid segment of claim 5, wherein said segment is 2000 nucleotides in length.

18. The isolated nucleic acid segment of claim 5, wherein the number of contiguous nucleotides is 20.

19. The isolated nucleic acid segment of claim 5, wherein the number of contiguous nucleotides is 25.

20. The isolated nucleic acid segment of claim 5, wherein the number of contiguous nucleotides is 30.

21. The isolated nucleic acid segment of claim 5, wherein the number of contiguous nucleotides is 35.

22. The isolated nucleic acid segment of claim 5, wherein the number of contiguous nucleotides is 50.

23. An expression cassette comprising a polynucleotide encoding a myocardin polypeptide operably linked to a regulatory sequence.

24. The expression cassette of claim 23, wherein the polynucleotide encodes a polypeptide having an amino acid sequence of SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30.

25. The expression cassette of claim 24, wherein the polynucleotide sequence comprises SEQ ID NO:1, SEQ ID NO:25, SEQ ID NO:27 or SEQ ID NO:29.

26. The expression cassette of claim 23, wherein said regulatory sequence comprises a promoter heterologous to the coding sequence.

27. The expression cassette of claim 26, wherein said promoter is a tissue specific promoter.

28. The expression cassette of claim 27, wherein said promoter is a muscle specific promoter.

29. The expression cassette of claim 28, wherein said muscle specific promoter is myosin light chain-2 promoter, alpha actin promoter, troponin 1 promoter, Na+/Ca2+ exchanger promoter, dystrophin promoter, creatine kinase promoter, alpha7 integrin promoter, brain natriuretic peptide promoter, alpha B-crystallin/small heat shock protein promoter, alpha myosin heavy chain promoter or atrial natriuretic factor promoter.

30. The expression cassette of claim 28, wherein said muscle specific promoter is a cardiac muscle specific promoter.

31. The expression cassette of claim 30, wherein said cardiac muscle specific promoter is a-myosin heavy chain or ANF.

32. The expression cassette of claim 23, wherein said promoter is an inducible promoter.

33. The expression cassette of claim 23, wherein said promoter is a constitutive promoter.

34. The expression cassette of claim 23, wherein said expression cassette is contained in a gene delivery vector.

35. The expression cassett of claim 34, wherein said gene delivery vector is a viral vector.

36. The expression cassette of claim 35, wherein said viral vector is a retroviral vector, an adenoviral vector, an adeno-associated viral vector, a vaccina viral vector, a herpesviral vector, a polyoma viral construct or a Sindbis viral vector.

37. The expression cassette of claim 23, wherein said expression cassette further comprises a polyadenylation signal.

38. The expression cassette of claim 23, wherein said expression cassette further comprises a second polynucleotide encoding a second polypeptide.

39. The expression cassette of claim 38, wherein said second polypeptide is a cardiac transcription factor.

40. A transformed host cell comprising a polynucleotide encoding a myocardin polypeptide and a promoter heterologous to the polypeptide coding region, wherein said promoter directs expression of said myocardin polypeptide.

41. The transformed host cell of claim 40, further defined as a prokaryotic host cell.

42. The transformed host cell of claim 40, further defined as an eukaryotic host cell.

43. A method of using a host cell comprising an expression cassette comprising a polynucleotide encoding a myocardin polypeptide and a promoter active in said host cell comprising culturing the host cell under conditions suitable for the expression of the myocardin polypeptide.

44. A peptide of 8 to about 50 residues comprising at least 8 consecutive residues of SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30.

45. The peptide of claim 44, wherein said peptide comprises 10 consecutive residues of SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30.

46. The peptide of claim 44, wherein said peptide comprises 12 consecutive residues of SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30.

47. A fusion protein comprising a myocardin protein or peptide fused to a second protein or peptide.

48. A method of modulating the phenotype of a non-cardiomyocyte cell to include one or more phenotypic functions of a cardiomyocyte cell comprising introducing into said non-cardiac cell an expression cassette comprising a polynucleotide encoding a myocardin polypeptide and a promoter active in said non-cardiac cell, wherein said promoter directs the expression of said polypeptide.

49. The method of claim 48, wherein said non-cardiomyocyte cell is a fibroblast.

50. The method of claim 48, wherein said method further comprises measuring cardiac lineage markers.

51. The method of claim 48, wherein said expression cassette further comprises a second polynucleotide encoding a second polypeptide.

52. The method of claim 51, wherein said second polypeptide is a cardiac transcription factor.

53. The method of claim 52, wherein said cardiac transcription factor is GATA4.

54. The method of claim 51, wherein said second polynucleotide is under the control of a second promoter.

55. The method of claim 51, wherein said first and second polynucleotide are the under control of the same promoter.

56. The method of claim 48, wherein said method further comprises introducing a second expression cassette into said non-cardiomyocyte cells, wherein said second expression cassette comprises a polynucleotide encoding a second polypeptide and a second promoter active in said non-cardiomyocyte cells, wherein said second promoter directs the expression of said second polypeptide.

57. The method of claim 50, wherein measuring comprises RNA hybridzation.

58. The method of claim 50, wherein measuring comprises PCR.

59. The method of claim 50, wherein measuring comprises RT-PCR.

60. The method of claim 50, wherein measuring comprises Western analysis.

61. A method of generating a cardiomyocyte comprising introducing into a cardiac fibroblast an expression vector comprising a polynucleotide encoding a myocardin polypeptide and a promoter active in said fibroblast, wherein said promoter directs the expression of said polypeptide.

62. The method of claim 61, wherein said expression vector comprises a lipid-based vector.

63. The method of claim 61, wherein said expression vector comprises a viral vector.

64. The method of claim 63, wherein said viral vector is a retroviral vector, an adenoviral vector, an adeno-associated viral vector, a vaccina viral vector, a herpesviral vector, a polyoma viral construct or a Sindbis viral vector.

65. The method of claim 61, wherein said promoter is heterologous to the coding sequence.

66. The method of claim 61, wherein said promoter is a tissue specific promoter.

67. The method of claim 66, wherein said promoter is a muscle specific promoter.

68. The method of claim 67, wherein said muscle specific promoter is a cardiac muscle specific promoter.

69. The method of claim 61, wherein said expression cassette further comprises a second polynucleotide encoding a second polypeptide.

70. The method of claim 69, wherein said second polypeptide is a cardiac transcription factor.

71. The method of claim 70, wherein said cardiac transcription factor is GATA4.

72. The method of claim 69, wherein said second polynucleotide is under the control of a second promoter active in a cardiac fibroblast.

73. The method of claim 69, wherein said first and second polynucleotide are under the control of the same promoter.

74. The method of claim 61, wherein said method further comprises introducing into said fibroblasts a said second expression cassette comprising a polynucleotide encoding a second polypeptide and a second promoter active in said fibroblast, wherein said second promoter directs the expression of said second polypeptide.

75. The method of claim 61, wherein said expression cassette further comprises a polyadenylation site.

76. The method of claim 61, wherein said expression cassette further comprises a selectable marker.

77. The method of claim 76, wherein said selectable marker is an immunologic marker.

78. A method of stimulating cardiac tissue regeneration comprising inhibiting the function of myocardin in a post-mitotic cardiomyocyte.

79. The method of claim 78, wherein inhibiting comprises providing to said post-mitotic cardiomyocyte an antisense nucleic acid that inhibits transcription or translation of a myocardin mRNA.

80. The method of claim 79, wherein providing comprises introducing into said post-mitotic cardiomyocyte an expression cassette encoding myocardin antisense RNA and a promoter active in said cardiomyocytes.

81. A method of expressing a myocardin polypeptide in a host cell comprising introducing into said host cells an expression vector comprising a polynucleotide encoding a myocardin polypeptide, said polynucleotide being positioned under control of a promoter operable in said host cell.

82. A monoclonal antibody that binds immunologically to a polypeptide comprising SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30 or an antigenic fragment thereof.

83. A polyclonal antisera, antibodies of which bind immunologically to a polypeptide comprising SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30 or an antigenic fragment thereof.

84. A hybridoma cell that produces a monoclonal antibody that binds immunologically to a polypeptide comprising SEQ ID NO:2, SEQ ID NO:26, SEQ ID NO:28 or SEQ ID NO:30 or an antigenic fragment thereof.

85. A non-human transgenic animal comprising an expression cassette, wherein said expression cassette comprises a polynucleotide encoding a myocardin peptide or protein and a promoter operable in eukaryotic cells, said promoter being heterologous to the myocardin peptide or protein encoding region.

86. The animal of claim 85, wherein said expression cassette further comprises a selectable marker.

87. The animal of claim 85, wherein said promoter is constitutive.

88. The animal of claim 85, wherein said promoter is tissue specific.

89. The animal of claim 85, wherein said promoter is inducible.

90. The animal of claim 85, wherein said animal is a mouse.

91. A non-human transgenic animal comprising a defective germ-line myocardin allele.

92. The non-human transgenic animal of claim 91, comprising two defective germ-line myocardin alleles.

93. A method of treating a heart disease, including cardiomyopathy comprising administering to an animal suffering therefrom an expression cassette comprising a polynucleotide encoding a myocardin peptide or protein and a promoter operable in eukaryotic cells.

94. The method of claim 93, wherein said cardiomyopathy is myocardial infarction or hypertension.

95. The method of claim 93, wherein said promoter is a cardiac specific promoter.

96. The method of claim 93, wherein said expression cassette is comprised within a replication-defective expression vector.

97. The method of claim 96, wherein said replication defective expression vector is a viral vector.

98. The method of claim 97, wherein said viral vector is a retroviral vector, an adenoviral vector, an adeno-associated viral vector, a vaccina viral vector, a herpesviral vector, a polyoma viral construct or a Sindbis viral vector.

99. A method of treating a heart disease, including cardiomyopathy comprising the step of providing to an animal suffering therefrom a myocardin antisense nucleic acid.

100. A method of decreasing mortality in a subject with heart failure comprising inhibiting the function of myocardin in post-mitotic cardiomyocytes in the subject.

101. A method of decreasing mortality in a subject with heart failure comprising increasing the level of myocardin in fibroblasts to generate cardiomyocytes in the subject.

102. A method of decreasing morbidity in a subject with heart failure comprising inhibiting the function of myocardin in post-mitotic cardiomyocytes in the subject.

103. A method of decreasing morbidity in a subject with heart failure comprising increasing the level of myocardin in fibroblasts to generate cardiomyocytes in the subject.

104. A method of screening for a candidate substance for an effect on myocardin regulation of cardiomyocyte development comprising:

(a) providing myocardin and GATA to a cell;
(b) admixing myocardin and GATA in the presence of said candidate substance; and (c) measuring the effect of said candidate substance on the expression of a cardiac lineage marker, wherein a difference in the expression of said cardiac lineage marker, as compared to an untreated cell, indicates that said candidate substance effects myocardin regulation of cardiomyocyte development.

105. The method of claim 104, wherein measuring comprises RNA hybridization.

106. The method of claim 104, wherein measuring comprises PCR.

107. The method of claim 104, wherein measuring comprises RT-PCR.

108. The method of claim 104, wherein measuring comprises immunologic detection of myocardin.

109. The method of claim 104, wherein measuring comprises ELISA.

110. The method of claim 104, wherein measuring comprises immunohisotchemistry.

111. The method of claim 104, wherein said cell is located in an animal.

112. The method of claim 104, wherein said cell is a fibroblast.

113. The method of claim 104, wherein said cell is a cardiomyocyte.

114. The method of claim 104, wherein said cardiac lineage marker is Nkx2.5.

115. The method of claim 104, wherein said modulator increases the expression of said cardiac lineage marker.

116. The method of claim 104, wherein said modulator decreases the expression of said cardiac lineage marker.

117. A method of screening for a modulator of myocardin expression comprising:
(a) providing a cell that expresses a myocardin polypeptide;
(b) contacting said myocardin polypeptide with a candidate substance; and (c) measuring the expression of myocardin, wherein a difference in myocardin expression, indicates that said candidate substance is a modulator of myocardin expression.

118. The method of claim 117, wherein said modulator enhances myocardin expression.

119. The method of claim 117, wherein said modulator inhibits myocardin expression.

120. The method of claim 117, wherein said candidate modulator is a pharmaceutical composition.

121. A method of screening a candidate substance for myocardin binding activity comprising:
(a) providing a myocardin polypeptide;
(b) contacting the myocardin polypeptide with the candidate substance; and (c) determining the binding of the candidate substance to the myocardin polypeptide.

122. The method of claim 121, wherein the assay is performed in a cell free system.

123. The method of claim 121, wherein the assay is performed in a cell.

124. The method of claim 121, wherein the assay is performed in vivo.

125. The method of claim 121, wherein said candidate substance is an inhibitor of myocardin.

126. The method of claim 121, wherein said candidate substance is an enhancer of myocardin.