Effects of diabetes on rodent cardiac thyroid hormone receptor and isomyosin expression

American Journal of Physiology - Endocrinology and Metabolism

Volumn 272, Issue 5 35-5, 1997, Pages

  Haddad, F ^a   Bodell, P W ^a   McCue, S A ^a   Baldwin, K M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

3,5,3' triiodothyronine binding; cardiac nuclei; gel mobility shift assay; nuclear extract; thyroid response element

Indexed keywords

LIOTHYRONINE; MYOSIN ADENOSINE TRIPHOSPHATASE ISOENZYME; MYOSIN HEAVY CHAIN; THYROID HORMONE RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; FEMALE; GEL MOBILITY SHIFT ASSAY; HEART MUSCLE CELL; HORMONE BINDING; HORMONE RESPONSIVE ELEMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; STREPTOZOCIN DIABETES;

EID: 0030974098     PISSN: 01931849     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpendo.1997.272.5.e856     Document Type: Article

References (35)

1. Alpert, N. R., and L. A. Mullieri. Functional consequences of altered cardiac myosin isoenzymes. Med. Sci. Sports Exercise 18: 309-313, 1986.
2. Ashizawa, K., and S. Y. Cheng. Regulation of thyroid hormone receptor-mediated transcription by a cytosol protein. Proc. Natl. Acad. Sci. USA 89: 9277-9281, 1992.
3. Chomczynski, P. A reagent for the single-step simultaneous isolation of RNA, DNA, and proteins from cell and tissue samples. Biotechniques 15: 532-537, 1993.
4. Dillmann, W. H. Diabetes and thyroid-hormone-induced changes in cardiac function and their molecular basis. Annu. Rev. Med. 40: 373-394, 1989.
5. Dillmann, W. H. Influence of thyroid hormone administration on myosin ATPase activity and myosin isoenzyme distribution in the heart of diabetic rats. Metabolism 31: 199-204, 1982.
6. 2+-myosin ATPase activity and changes myosin isoenzyme distribution in the diabetic rat heart. Am. J. Physiol. 248 (Endocrinol. Metab. 11): E602-E606, 1985.
7. Edwards, J. G., J. J. Bahl, I. L. Flink, S. Y. Cheng, and E. Morkin. Thyroid hormone influences β myosin heavy chain expression. Biochem. Biophys. Res. Commun. 199: 1482-1488, 1994.
8. Flink, I. L., and E. Morkin. Alternatively processed isoforms of cellular nucleic acid-binding protein interact with a suppressor region of the human beta-myosin heavy chain gene. J. Biol. Chem. 270: 6959-6965, 1995.
9. Flink, I. L., and E. Morkin. Interaction of thyroid hormone receptors with strong and weak cis-acting elements in the human α-myosin heavy chain gene promoter. J. Biol. Chem. 265: 11233-11237, 1990.
10. 4. Am. J. Physiol. 244 (Heart Circ. Physiol. 13): H592-H598, 1983.
11. Glass, C. K., and J. M. Holloway. Regulation of gene expression by the thyroid hormone receptor. Biochim. Biophys. Acta 1032: 157-176, 1990.
12. Glass, C. K., J. M. Holloway, O. V. Devary, and M. G. Rosenfeld. The thyroid hormone receptor binds with opposite transcriptional effects to a common sequence motif in thyroid hormone and estrogen response elements. Cell 54: 313-323, 1988.
13. Haddad, F., P. W. Bodell, S. A. McCue, and K. M. Baldwin. Food restriction-induced transformations in cardiac functional and biochemical properties in rats. J. Appl. Physiol. 74: 606-612, 1993.
14. Haddad, F., M. Masatsugu, P. W. Bodell, A. Qin, S. A. McCue, R. E. Herrick, and K. M. Baldwin. Role of thyroid hormone and insulin in control of cardiac isomyosin expression. J. Mol. Cell. Cardiol. 29: 559-569, 1997.
15. Hoh, J. F. Y., P. A. McGrath, and H. T. Hale. Electrophoretic analysis of multiple forms of rat cardiac myosin: effect of hypophysectomy and thyroxine replacement. J. Mol. Cell. Cardiol. 10: 11053-11076, 1978.
16. Izumo, S., and V. Mahdavi. Thyroid hormone receptor alpha isoforms generated by alternative splicing differentially activate myosin HC gene transcription. Nature 334: 593-595, 1988.
17. Karin, M., H. F. Yang-Yen, J. C. Chambard, T. Deng, and F. Saatcioglu. Various modes of gene regulation by nuclear receptors for steroid and thyroid hormones. Eur. J. Clin. Pharmacol. 45, Suppl. 1: S9-S15, 1993.
18. Labarca, C., and K. Paigen. A simple, rapid, and sensitive DNA assay procedure. Anal. Biochem. 102: 344-352, 1980.
19. Liew, C. C., G. Jackowski, T. Ma, and M. J. Sole. Nonenzymatic separation of myocardial cell nuclei from whole heart tissue. Am. J. Physiol. 244 (Cell Physiol. 13): C3-C10, 1983.
20. Lompre, A. M., B. Nadal-Ginard, and V. Mahdavi. Expression of the cardiac alpha- and beta-myosin heavy chain genes is developmentally and hormonally regulated. J. Biol. Chem. 259: 6437-6446, 1984.
21. Mahdavi, V., M. Perisamy, and B. Nadal-Ginard. Molecular characterization of two myosin heavy chain genes expressed in the adult heart. Nature 297: 659-964, 1982.
22. Morris, G. S., K. M. Baldwin, J. M. Lash, R. L. Hamlin, and W. M. Sherman. Exercise alters cardiac myosin isozyme distribution in obese Zucker and Wistar rats. J. Appl. Physiol. 69: 380-383, 1990.
23. Morris, G. S., R. E. Herrick, and K. M. Baldwin. Dietary carbohydrates modify cardiac myosin isoenzyme profiles of semistarved rats. Am. J. Physiol. 256 (Regulatory Integrative Comp. Physiol. 25): R976-R981, 1989.
24. Murray, M. B., and H. C. Towle. Identification of nuclear factors that enhance binding of the thyroid hormone receptor to a thyroid hormone response element. Mol. Endocrinol. 3: 1434-1442, 1989.
25. Rottman, J. N., W. R. Thompson, B. Nadal-Ginard, and V. Mahdavi. Myosin heavy chain gene expression: interplay of cis and trans factors determines hormonal and tissue specificity. In: The Dynamic State of Muscle Fibers, edited by D. Pette. New York: de Gruyter, 1990, p. 3-16.
26. Rupp, H., R. Jacob, and N. S. Dhalla. Signal transduction of myosin heavy chain expression in the diahetic heart. In: The Diabetic Heart, edited by M. Nagano and N. S. Dhalla, New York: Raven, 1991, p. 271-279.
27. Schaffer, S. W. M. S. Mozaffari, M. Artman, and G. L. Wilson. Basis for myocardial mechanical defects associated with non-insulin-dependent diabetes. Am. J. Physiol. 256 (Endocrinol. Metab. 19): E25-E30, 1989.
28. Sugawara, A., P. M. Yen, J. W. Apriletti, R. C. Ribeiro, D. B. Sacks, J. D. Baxter, and W. W. Chin. Phosphorylation selectively increases triiodothyronine receptor homodimer binding to DNA. J. Biol. Chem. 269: 433-437, 1994.
29. Swoap, S. J., F. Haddad, P. Bodell, and K. M. Baldwin. Control of β-myosin heavy chain expression in systemic hypertension and caloric restriction in the rat heart. Am. J. Physiol. 269 (Cell Physiol. 38): C1025-C1033, 1995.
30. Swoap, S. J., F. Haddad, P. Bodell, and K. M. Baldwin. Effect of chronic energy deprivation on cardiac thyroid hormone receptor and myosin isoform expression. Am. J. Physiol. 266 (Endocrinol. Metab. 29): E254-E260, 1994.
31. Tahiliani, A. G., and J. H. McNeill. Prevention of diabetes-induced myocardial dysfunction in rats by methyl palmoxirate and triiodothyronine treatment. Can. J. Physiol. Pharmacol. 63: 925-931, 1985.
32. Thompson, W. R., B. Nadal-Ginard, and V. Mahdavi. A myoD1-independent muscle-specific enhancer controls the expression of the β-myosin heavy chain gene in skeletal and cardiac muscle cells. J. Biol. Chem. 266: 22678-22688, 1991.
33. Umeda, P. K., R. L. Carter, R. S. Hall, J. M. Welborn, and L. B. Bugaiski. Regulation of the myosin heavy chain β promoter in skeletal and cardiac myocytes. In: The Dynamic State of Muscle Fibers. New York: de Gruyter, 1990, p. 61-74.
34. Zahradka, P., D. E. Larson, and B. H. Sells. RNA polymerase II-directed gene transcription by rat skeletal muscle nuclear extracts. Exp. Cell Res. 185: 8-20, 1989.
35. Zak, R., J. Etlinger, and D. A. Fischman. Studies on the fractionation of skeletal and heart muscle. In: Research in Muscle Development and Muscle Spindle, edited by B. Q. Banker, R. J. Ptyzbylski, J. P. V. D. Menlen, and M. Victor. Amsterdam: Exerpta Medica, 1972, p. 163-175.