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BIOGRAPHICAL SKETCH Provide the following information for the key
personnel and other significant contributors. |
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NAME Thomas Alexander Cooper |
POSITION TITLE Professor |
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eRA COMMONS USER NAME tcooper |
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EDUCATION/TRAINING (Begin with baccalaureate or other initial professional education, such as nursing, and include postdoctoral training.) |
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INSTITUTION AND LOCATION |
DEGREE (if
applicable) |
YEAR(s) |
FIELD OF STUDY |
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B.S. |
1977 |
Biology |
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M.D. |
1982 |
Medicine |
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A. Positions and Honors.
Positions and Employment
1982-1986: Postdoctoral Fellow, laboratory of Dr.
Charles P. Ordahl, Department of Anatomy, University of California, San
Francisco, CA
1986-1989: Assistant Research Anatomist,
Department of Anatomy,
1989-1997: Assistant Professor, Department of
Pathology (primary appointment), Baylor College of Medicine,
1990-present: Assistant Professor, Department of
Molecular and Cellular Biology (joint appointment), Baylor College of Medicine,
1997-2003: Associate Professor, Department of
Pathology, Baylor
2003-present Professor, Department of Pathology, Baylor
College of Medicine,
2004-present Professor, Department of Molecular and
Cellular Biology (joint appointment), Baylor College of Medicine,
Honors
and Awards:
1981: NIH Medical Research Trainee Predoctoral Award
1982-1985: NIH Postdoctoral Fellowship
1985-1986: Bank
of
1991-1994: March of Dimes Basil O’Connor Starter Scholar Research Award
1992-1997: Established Investigator, American Heart Association
1999 Michael E. DeBakey, M.D. Excellence in Research Award
2003 S. Donald Greenberg Chair in Pathology
B.
Selected peer-reviewed publications in chronological order.
1. Ordahl, C.P., Cooper, T.A. (1983). Strong homology in promoter and 3’-untranslated regions of chick and rat a-actin genes. Nature 303, 348-349.
2. Ordahl,
C.P., Peng,
3. Cooper, T.A. and Ordahl, C.P. (1984). A single troponin T gene is governed by two different regulatory programs in cardiac and skeletal muscle development. Science 226, 979-982.
4. Ordahl, C.P., Evans, G.L., Cooper, T.A., Kunz, G., Perriard, J.C. (1985). Complete amino acid sequence of chick muscle creatine kinase. J. Biol. Chem. 259, 15224-15231.
5. Cooper, T.A. and Ordahl, C.P. (1985). A single cardiac troponin T gene generates embryonic and adult isoforms via developmentally regulated alternate splicing. J. Biol. Chem. 260, 11140-11148.
6. Mar, J.H., Antin, P.B., Cooper, T.A., and Ordahl, C.P. (1988). Analysis of the upstream regions governing expression of the chicken cardiac troponin T gene in embryonic cardiac and skeletal muscle cells. J. Biol. Chem. 107, 573-585.
7. Cooper, T.A., Cardone, M.H., and Ordahl, C.P. (1988). Cis requirements for alternative splicing of the cardiac troponin T pre-mRNA. Nucl. Acids Res. 16, 8443-8465.
8. Cooper, T.A. and Ordahl, C.P. (1989). Nucleotide substitutions within the cardiac troponin T alternative exon disrupt pre-mRNA alternative splicing. Nucl. Acids Res.17, 7905-7921.
9. Cooper, T.A. (1992). In vitro splicing of cardiac troponin T precursors: exon mutations disrupt splicing of the upstream intron. J. Biol. Chem. 267, 5330-5338.
10. Xu, R., Teng, J., and Cooper, T.A. (1993). The cardiac troponin T alternative exon contains a novel purine-rich positive splicing element. Mol. Cell. Biol. 13, 3660-3674.
11. Lee, A.B., and Cooper, T.A. (1995). An improved direct PCR screen of bacterial colonies. BioTechniques 18, 225-226.
12. Humphrey,
M.B.,
13. Ramchatesingh, J., Zahler, A.M., Neugebauer, K.M., Roth, M.B., and Cooper, T.A. (1995). A subset of SR proteins activates splicing of the cardiac troponin T alternative exon by direct interactions with an exonic enhancer. Mol. Cell. Biol. 15, 4898-4907.
14. Ryan, K.J. and Cooper, T.A. (1996) Muscle-specific splicing enhancers regulate inclusion of the cardiac troponin T alternative exon in embryonic skeletal muscle. Mol. Cell. Biol. 16, 4014-4023.
15. Coulter, L., Landree, M., and Cooper, T.A. (1997) Identification of a new class of exonic splicing enhancers by in vivo selection. Mol. Cell. Biol. 17, 2143-2150.
16. Elrick, L.L., Humphrey, M.B., Cooper, T.A., and Berget, S.M. (1998) A short sequence within two purine-rich enhancers determines 5' splice site specificity. Mol. Cell. Biol. 18, 343-352.
17. Philips, A.V., Timchenko, L.T., and Cooper, T.A. (1998) Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. Science 280, 737-741, also see accompanying "Perspectives" in same issue.
18. Cooper, T.A. (1998) Muscle-specific splicing of a heterologous exon mediated by a single muscle-specific splicing enhancer from the cardiac troponin T gene. Mol. Cell. Biol. 18, 4519-4525.
19. Stoss, O., Cooper, T.A., and Stamm, S. (1999) Alternative splicing determines the intracellular localization of the muscle specific nucleolar proteins NOP30-1 and NOP30-2. J. Biol. Chem. 274, 10951-10962.
20. Stark, J.M., Cooper, T.A., Roth M.B. (1999) The relative strengths of SR protein-mediated associations of alternative and constitutive exons can influence alternative splicing. J. Biol. Chem. 274, 29838-29842.
21. The International Myotonic Dystrophy Consortium (IDMC) (2000) New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1). Neurology 54, 1218-1221.
22. Ryan, K.J., Charlet-B., N., and Cooper, T.A. (2000) Binding of purH to a muscle-specific splicing enhancer correlates with exon inclusion in vivo. J. Biol. Chem. 275, 20618-20626.
23. Ladd, A.N., Charlet-B., N., and Cooper, T.A. (2001) The CELF family of RNA binding proteins is implicated in cell-specific and developmentally regulated alternative splicing Mol. Cell. Biol. 21, 1285-1296.
24. Stickeler,
E.,
25. Savkur, R., Philips, A.V., and Cooper, T.A. (2001) Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy. Nat Genet. 29, 40-47.
26. Charlet-B.,
Singh, G, N.,
27. Charlet-B., Savkur, R., Singh, G, N., Philips, A.V., Grice, E.A., and Cooper, T.A. (2002) Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. Mol. Cell, 10, 45-53.
28. Gromak,
N., Matlin, A.J., Cooper, T.A., and Smith, C.W.J. (2003) Antagonistic
regulation of alpha-actinin alternative splicing by CELF proteins and
polypyrimidine tract binding protein. RNA 9, 443-456.
29. Singh,
G., Charlet-B., N., Han, J., and Cooper, T.A. (2004) ETR-3 and CELF4 protein domains
required for RNA binding and splicing activity in vivo. Nucl. Acids Res. 32, 1232-1241.
30. Ladd,
A.N.,
31. Savkur,
R.S., Philips, A.V., Cooper, T.A.,
32. Ladd,
A.N. and Cooper, T.A.
(2004) Nuclear-cytoplasmic localization of the RNA binding protein ETR-3
is controlled by multiple localization elements. J. Cell Science 117,
3519-3529.
33. Ho, T., Charlet-B., N., Poulos, M., Singh, G., Swanson, M.S., and Cooper, T.A. (2004) Muscleblind proteins regulate alternative splicing. EMBO J. 23, 3103-3112
34. Faustino, N.A. and Cooper, T.A. (2005) Identification of putative new splicing targets for ETR-3 using its SELEX sequences. Mol. Cell. Biol. 25, 879-887.
35. Ho, T., Bundman, D., Armstrong, D.L., and Cooper, T.A. (2005) Transgenic mice expressing CUG-BP1 reproduce the myotonic dystrophy pattern of splicing. Hum. Mol. Genet. 14, 1539-1547.
36. Han, J. and Cooper, T.A. (2005) Characterization of CELF splicing activation and repression domains in vivo. Nucl. Acids Res. 33, 2769-2780.
37. Ladd, A.L. Stenberg, M.G., Swanson, M.S., and Cooper, T.A. (2005) A dynamic balance between activation and repression regulates pre-mRNA alternative splicing during heart development. Dev. Dyn. 233, 783-793.
38. Ho, T., Savkur, R.S., Poulos, M., Mancini., M.M., Swanson, M.S., and Cooper, T.A. (2005) Co-localization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy. J. Cell Science 118 2923-2933.
39. Ladd,
A.N., Taffet, G.E., Hartley, C.,
40. Leroy, O., Wang, J., Maurage, C.A., Parent, M., Cooper, T., Buee, L., Sergeant, N., Andreadis, A., Caillet-Boudin, M.L. (2006) Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1 Biochim Biophys Acta. 1762, 460-467.
41. de Haro, M., Al-Ramahi, I,, De Gouyon, B., Ukani, L., Rosa, A., Faustino, N.A., Ashizawa, T., Cooper, T.A. and Botas, J. (2006) MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of Myotonic Dystrophy Type 1. Hum. Mol. Gen. 15, 2138-2145.
42. Singh, G, N. and Cooper, T.A. (2006) A minigene reporter for identification and analysis of cis elements and trans factors affecting pre-mRNA splicing. BioTechniques 41,177-181.
43. Orengo, J., Bundman, D., and Cooper, T.A. (2006) A bichromatic fluorescent reporter for cell-based screens of alternative splicing Nucl. Acids Res. 34, e148.
44. Wang,
G.S.,
45.
Invited
Articles and Reviews
46. Cooper, T.A. and Mattox, W. (1997) The regulation of splice site selection and its role in human disease. Amer. J. Hum. Gen. 61, 259-266.
47. Cooper, T.A. (1999) In vivo SELEX in vertebrate cells in "RNA-Protein Interactions", Susan R. Haynes, Ed.; Methods in Molecular Biology Series, John M. Walker, Ed., (Humana Press), Vol. 118, 405-417.
48. Cooper, T.A. (1999) Strategies for defining pre-mRNA cis elements that regulate cell specific splicing in "RNA-Protein Interactions", Susan R. Haynes, Ed.; Methods in Molecular Biology Series, John M. Walker, Ed., (Humana Press), vol. 118, 391-403.
49. Philips, A.V. and Cooper, T.A. (2000) RNA and human disease. Cell. Mol. Life Sci. 57, 235-249.
50. Cooper,
T.A. (2001) mRNA splicing: regulated
and differential. Encyclopedia of Life Sciences, Macmillan,
51. Cooper, T.A., (2001) Highlights of alternative splicing regulation session: Yes, no, maybe--A history of paradigm shifts. Science STKE, http://www.stke.org/cgi/content/full/OC_sigtrans;2001/105/pe35.
52. Ladd,
A.N., Cooper, T.A. (2002) Finding signals that
regulate alternative splicing in the post-genomic era. Genome Biology 3,
8.1-8.16.
53. Timchenko, L.T., Tapscott, S.J., Cooper, T.A., Monckton, D.G. (2002) Myotonic dystrophy: discussion of molecular basis. Adv Exp Med Biol. 516, 27-45.
54. Faustino, A. and Cooper, T.A. (2003) RNA splicing and human disease. Genes Dev. 17, 419-437.
55. Cooper, T.A. (2005) Alternative splicing regulation impacts heart development. Cell 120, 1-2.
56. Cooper, T. A. (2005) In vivo SELEX strategies, p. 840-852. In R. K. Hartmann, A. Bindereif, A. Schon, and E. Westhof (ed.), Handbook of RNA Biochemistry, vol. 2. Wiley-VCH Verlag GmbH and Co, Weinheim.
57. Cooper, T.A. (2005) Use of minigene systems to dissect alternative splicing elements. Methods 37, 331-340.
58.
59.
60. Ranum L.P. and Cooper, T.A. (2006) RNA-mediated neuromuscular disorders. Ann. Rev. Neuroscience 29, 259-277.
61. Cooper, T.A. (2006) A reversal of fortune for myotonic dystrophy? N. Engl. J. Med. 355, 1825-1827.
62. Cooper, T.A. (2007) Regulation of chloride ion conductance during skeletal muscle development and in disease. Amer. J. Physiol: Cell Physiology 292, C1245-1247.
63. Bland, C.S. and Cooper, T.A. (2007) Micromanaging alternative splicing during muscle differentiation Dev Cell 12, 171-172
64. Orengo, J.P. and Cooper, T.A. (2007) Alternative splicing in disease in Alternative splicing in the post-genomic era, B.R. Graveley and B. Blencowe, ed. Landes publishing. (In Press).
65. Wang, G.S. and Cooper T.A. (2007) Splicing in disease: disruption of the splicing code and the decoding machinery. Nature Rev. Genet. (In Press)
C.
Research Support.
ACTIVE
R01 HL 45565, (Yrs 14-17) Cooper 7/01/04-06/30/08
National of Heart Lung and Blood Institute
"Troponin T Alternative Splicing in Embryonic Heart"
The long term goal of this project is to understand the molecular basis for the regulation of pre-mRNA alternative splicing. The objectives are to characterize recently isolated regulators of muscle-specific alternative splicing during development, by transient transfection, and using a cell free splicing assay.
Role: PI
R01 AR/GM 45653, (Yrs
6-10) 3/1/04-2/28/09
National
"Molecular Pathogenesis of Myotonic Dystrophy"
The long term objective of this project is to understand the pathogenic mechanisms of myotonic dystrophy. The objectives are to determine the effects of CUG repeats on the function of a family of RNA binding proteins and to generate and study cellular and mouse models for myotonic dystrophy.
Role: PI
R01 GM076493-01 2/1/06-1/31/10
National
“Mechanisms of developmentally regulated splicing”
The long term goal of this proposal is to understand the mechanisms by which endogenous alternative splicing regulators modulate natural splicing transitions. A systematic large scale screen will identify alternative splicing events regulated during striated muscle development. The direct regulators and signaling events modifying the activities of the regulators will be identified.
Role: PI
Research Grant 1/1/07-12/31/09
Muscular Dystrophy Association
“An inducible mouse model for CNS manifestations of myotonic dystrophy”
The long term objective of this project is to understand the mechanism of pathogenesis of myotonic dystrophy in the CNS.
Role: PI