The circadian protein Clock localizes to the sarcomeric Z-disk and is a sensor of myofilament cross-bridge activity in cardiac myocytes

Biochemical and Biophysical Research Communications

Volumn 351, Issue 4, 2006, Pages 1054-1059

  Qi, Lixin ^a   Boateng, Samuel Y ^a  

^a UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Circadian; Clock; Cross bridge cycling; Myocytes; Myofilaments; Nuclear; Nucleo cytoplasmic shuttling; Z disk

Indexed keywords

2,3 BUTANEDIONE; CALCIUM; PHENYLEPHRINE; TRANSCRIPTION FACTOR CLOCK; VERAPAMIL;

ANIMAL CELL; ARTICLE; CELL FRACTIONATION; CELL NUCLEUS; CELLULAR DISTRIBUTION; CHROMOSOME TRANSLOCATION; CIRCADIAN RHYTHM; CONTROLLED STUDY; CYTOSKELETON; ENERGY EXPENDITURE; ENERGY RESOURCE; HEART MUSCLE CELL; IMMUNOHISTOCHEMISTRY; MYOFILAMENT; NEWBORN; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RAT; SENSOR;

ACTIVE TRANSPORT, CELL NUCLEUS; ANIMALS; CALCIUM; CELL NUCLEUS; DIACETYL; ENERGY METABOLISM; MICROFILAMENTS; MYOCARDIAL CONTRACTION; MYOCYTES, CARDIAC; PHENYLEPHRINE; RATS; RATS, SPRAGUE-DAWLEY; SARCOMERES; TRANS-ACTIVATORS; VERAPAMIL;

MAMMALIA;

EID: 33750839595     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.10.168     Document Type: Article

References (21)

1. Murali N.S., Svatikova A., and Somers V.K. Cardiovascular physiology and sleep. Front. Biosci. 8 (2003) s636-s652
2. Portman M.A. Molecular clock mechanisms and circadian rhythms intrinsic to the heart (Editorial). Circ. Res. 89 (2001) 1084
3. Young M.E., Alcorn J.L., Moravec C.S., Frazier O.H., and Taegtmeyer H. Intrinsic diurnal variations in cardiac metabolism and contractile function. Circulation 104 (2001) 2923-2931
4. Young M.E. The circadian clock within the heart: potential influence on myocardial gene expression, metabolism, and function. Am. J. Physiol.---Heart Circ. Physiol. 290 (2006) 1-16
5. Challet E., Caldelas I., Graff C., and Pevet P. Synchronization of the molecular clockwork by light- and food-related cues in mammals. Biol. Chem. 384 (2003) 711-719
6. Rudic R.D., McNamara P., Curtis A.M., Boston R.C., Panda S., Hogenesch J.B., and Fitzgerald G.A. BMAL1 and CLOCK, two essential components of the circadian clock, are involved in glucose homeostasis. PLoS Biol. 2 (2004) 1893-1899
7. Durgan D.J., Trexler N.A., Egbejimi O., McElfresh T.A., Suk H.Y., Petterson L.E., Shaw C.A., Hardin P.E., Bray M.S., Chandler M.P., Chow C.W., and Young M.E. The circadian clock within the cardiomyocyte is essential for responsiveness of the heart to fatty acids. J. Biol. Chem. 281 (2006) 24254-24269
8. Hardin P.E., and Yu W. Circadian transcription: passing the HAT to CLOCK. Cell 125 (2006) 424-426
9. Boateng S.Y., Hartman T.J., Ahluwalia N., Vidula H., Desai T.A., and Russell B. Inhibition of fibroblast proliferation in cardiac myocyte cultures by surface microtopography. Am. J. Physiol.---Cell Physiol. 285 (2003) C171-C182
10. Ramsby M.L., Makowski G.S., and Khairallah E.A. Differential detergent fractionation of isolated hepatocytes: biochemical, immunochemical and two-dimensional gel electrophoresis characterization of cytoskeletal and noncytoskeletal compartments. Electrophoresis 15 (1994) 265-277
11. S.Y. Boateng, R.J. Belin, D.L. Geenen, K.B. Margulies, J.L. Martin, M. Hoshijima, P.P. de Tombe, B. Russell, Cardiac dysfunction and heart failure are associated with abnormalities in the subcellular distribution and amounts of oligomeric muscle LIM protein, Am. J. Physiol. Heart Circ. Physiol. Sep 8 [Epub ahead of print] (2006).
12. Boateng S.Y., Seymour A.M., Bhutta N.S., Dunn M.J., Yacoub M.H., and Boheler K.R. Sub-antihypertensive doses of ramipril normalize sarcoplasmic reticulum calcium ATPase expression and function following cardiac hypertrophy in rats. J. Mol. Cell Cardiol. 30 (1998) 2683-2694
13. Boateng S.Y., Lateef S.S., Mosley W., Hartman T.J., Hanley L., and Russell B. RGD and YIGSR synthetic peptides facilitate cellular adhesion identical to that of laminin and fibronectin but alter the physiology of neonatal cardiac myocytes. Am. J. Physiol. Cell Physiol. 288 (2005) C30-C38
14. Cutolo M., and Masi A.T. Circadian rhythms and arthritis. Rheum. Dis. Clin. North Am. 31 (2005) 115-129
15. Hofman M.A. The human circadian clock and aging. Chronobiol. Int. 17 (2000) 245-259
16. Hoshijima M. Mechanical stress-strain sensors embedded in cardiac cytoskeleton: Z disk, titin, and associated structures. Am. J. Physiol. Heart Circ. Physiol. 290 (2006) H1313-H1325
17. Simpson P. Stimulation of hypertrophy of cultured neonatal rat heart cells through an alpha 1-adrenergic receptor and induction of beating through an alpha 1- and beta 1-adrenergic receptor interaction. Evidence for independent regulation of growth and beating. Circ. Res. 56 (1985) 884-894
18. Kim D.J., Park S.H., Lim C.S., Chun J.S., Kim J.K., and Song W.K. Cellular localization of integrin isoforms in phenylephrine-induced hypertrophic cardiac myocytes. Cell Biochem. Funct. 21 (2003) 41-48
19. Kanbe K., Inoue K., Xiang C., and Chen Q. Identification of clock as a mechanosensitive gene by large-scale DNA microarray analysis: downregulation in osteoarthritic cartilage. Mod. Rheumatol. 16 (2006) 131-136
20. Shweiki D. The physical imperative in circadian rhythm: a cytoskeleton-related physically resettable clock mechanism hypothesis. Med. Hypotheses 53 (1999) 413-420
21. i and contractile activity. Am. J. Physiol. 271 (1996) C01447-C01456