Different roles of H-ras for regulation of myosin heavy chain promoters in satellite cell-derived muscle cell culture during proliferation and differentiation

American Journal of Physiology - Cell Physiology

Volumn 297, Issue 4, 2009, Pages

  Scholz, Michael E ^a,d   Meissner, Joachim D ^a   Scheibe, Renate J ^a   Umeda, Patrick K ^b   Chang, Kin Chow ^c   Gros, Gerolf ^a   Kubis, Hans Peter ^a,e  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b and Clinical Center   (United States)

^c UNIVERSITY OF NOTTINGHAM   (United Kingdom)

^d UNIVERSITY OF ABERDEEN   (United Kingdom)

^e BANGOR UNIVERSITY   (United Kingdom)

Author keywords

Akt; Extracellular signal regulated protein kinase 1 2; Mammalian target of rapamycin; Mitogen activated protein kinase; Phosphosinositol 3 kinase

Indexed keywords

2 MORPHOLINO 8 PHENYLCHROMONE; LUCIFERASE; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1; MYOSIN HEAVY CHAIN; MYOSIN HEAVY CHAIN BETA; MYOSIN HEAVY CHAIN I; MYOSIN HEAVY CHAIN IID; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; RAS PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CELL PROLIFERATION; CONTROLLED STUDY; FAST MUSCLE FIBER; GENE CONSTRUCT; GENE OVEREXPRESSION; MUSCLE CELL; MUSCLE DEVELOPMENT; MYOTUBE; NONHUMAN; ONCOGENE H RAS; PRIORITY JOURNAL; PROMOTER REGION; RABBIT; REGULATORY MECHANISM; REPORTER GENE; SATELLITE CELL; SIGNAL TRANSDUCTION; SLOW MUSCLE FIBER; TRANSIENT TRANSFECTION;

ANIMALS; CELL DIFFERENTIATION; CELL PROLIFERATION; CELLS, CULTURED; CHROMONES; GENES, RAS; MAP KINASE SIGNALING SYSTEM; MORPHOLINES; MYOSIN HEAVY CHAINS; PHOSPHATIDYLINOSITOL 3-KINASES; PROMOTER REGIONS, GENETIC; PROTO-ONCOGENE PROTEINS P21(RAS); RABBITS; SATELLITE CELLS, SKELETAL MUSCLE; SIGNAL TRANSDUCTION;

MAMMALIA; ORYCTOLAGUS CUNICULUS;

EID: 70349925549     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00567.2008     Document Type: Article

References (43)

1. Adams GR. Satellite cell proliferation and skeletal muscle hypertrophy. Appl Physiol Nutr Metab 31: 782-790, 2006.
2. Allen DL, Leinwand LA. Intracellular calcium and myosin isoform transitions. Calcineurin and calcium-calmodulin kinase pathways regulate preferential activation of the IIa myosin heavy chain promoter. J Biol Chem 277: 45323-45330, 2002.
3. Allen DL, Sartorius CA, Sycuro LK, Leinwand LA. Different pathways regulate expression of the skeletal myosin heavy chain genes. J Biol Chem 276: 43524-43533, 2001. (Pubitemid 37383910)
4. Allen DL, Weber JN, Sycuro LK, Leinwand LA. Myocyte enhancer factor-2 and serum response factor binding elements regulate fast Myosin heavy chain transcription in vivo. J Biol Chem 280: 17126-17134, 2005.
5. Andres V, Walsh K. Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis. J Cell Biol 132: 657-666, 1996. (Pubitemid 26069245)
6. Bassel-Duby R, Olson EN. Signaling pathways in skeletal muscle remodeling. Annu Rev Biochem 2006. (Pubitemid 44118024)
7. Bennett AM, Tonks NK. Regulation of distinct stages of skeletal muscle differentiation by mitogen-activated protein kinases. Science 278: 1288-1291, 1997.
8. Black BL, Olson EN. Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins. Annu Rev Cell Dev Biol 14: 167-196, 1998.
9. Blau HM, Webster C. Isolation and characterization of human muscle cells. Proc Natl Acad Sci USA 78: 5623-5627, 1981. (Pubitemid 12245202)
10. Booth FW, Baldwin KM. Muscle plasticity: Energy demand/supply processes. In: Handbook of Physiology. Exercise: Regulation and Integration of Multiple Systems. Bethesda, MD: Am. Physiol. Soc, 1996, sect. 12, chapt.24, p. 1075-1123.
11. Cannon-Carlson S, Tang J. Modification of the Laemmli sodium dodecyl sulfate-polyacrylamide gel electrophoresis procedure to eliminate artifacts on reducing and nonreducing gels. Anal Biochem 246: 146-148, 1997. (Pubitemid 27100519)
12. Charge SB, Rudnicki MA. Cellular and molecular regulation of muscle regeneration. Physiol Rev 84: 209-238, 2004. (Pubitemid 38049880)
13. Chong H, Vikis HG, Guan KL. Mechanisms of regulating the Raf kinase family. Cell Signal 15: 463-469, 2003. (Pubitemid 36292166)
14. Cribbs LL, Shimizu N, Yockey CE, Levin JE, Jakovcic S, Zak R, Umeda PK. Muscle-specific regulation of a transfected rabbit myosin heavy chain beta gene promoter. J Biol Chem 264: 10672-10678, 1989. (Pubitemid 19161641)
15. Davis RL, Weintraub H, Lassar AB. Expression of a single transfected cDNA converts fibroblasts to myoblasts. Cell 51: 987-1000, 1987.
16. Degens H. Age-related skeletal muscle dysfunction: causes and mechanisms. J Musculoskelet Neuronal Interact 7: 246-252, 2007. (Pubitemid 350238152)
17. Downward J. The ras superfamily of small GTP-binding proteins. Trends Biochem Sci 15: 469-472, 1990.
18. Feig LA, Cooper GM. Inhibition of NIH 3T3 cell proliferation by a mutant ras protein with preferential affinity for GDP. Mol Cell Biol 8: 3235-3243, 1988.
19. Folland JP, Williams AG. The adaptations to strength training: morphological and neurological contributions to increased strength. Sports Med 37: 145-168, 2007.
20. Gibson MC, Schultz E. The distribution of satellite cells and their relationship to specific fibre types in soleus and extensor digitorum longus muscles. Anat Rec 202: 329-337, 1982.
21. Gibson MC, Schultz E. Age-related differences in absolute numbers of skeletal muscle satellite cells. Muscle Nerve 6: 574-580, 1983.
22. Gredinger E, Gerber AN, Tamir Y, Tapscott SJ, Bengal E. Mitogen-activated protein kinase pathway is involved in the differentiation of muscle cells. J Biol Chem 273: 10436-10444, 1998. (Pubitemid 28227653)
23. Jiang H, Jordan T, Li J, Li H, DiMario JX. Innervation-dependent and fibre type-specific transcriptional regulation of the slow myosin heavy chain 2 promoter in avian skeletal muscle fibres. Dev Dyn 231: 292-302, 2004. (Pubitemid 39238055)
24. Konieczny SF, Drobes BL, Menke SL, Taparowsky EJ. Inhibition of myogenic differentiation by the H-ras oncogene is associated with the down regulation of the MyoD1 gene. Oncogene 4: 473-481, 1989.
25. Kuang S, Rudnicki MA. The emerging biology of satellite cells and their therapeutic potential. Trends Mol Med 14: 82-91, 2008.
26. Kubis HP, Haller EA, Wetzel P, Gros G. Adult fast myosin pattern and Ca2+-induced slow myosin pattern in primary skeletal muscle culture. Proc Natl Acad Sci USA 94: 4205-4210, 1997. (Pubitemid 27180524)
27. Lassar AB, Thayer MJ, Overell RW, Weintraub H. Transformation by activated ras or fos prevents myogenesis by inhibiting expression of MyoD1. Cell 58: 659-667, 1989. (Pubitemid 19210960)
28. Meissner JD, Chang KC, Kubis HP, Nebreda AR, Gros G, Scheibe RJ. The p38alpha /beta MAP kinases mediate recruitment of CBP to preserve fast myosin heavy chain IId/x gene activity in myotubes. J Biol Chem 282: 7265-7275, 2007.
29. Meissner JD, Gros G, Scheibe RJ, Scholz M, Kubis HP. Calcineurin regulates slow myosin, but not fast myosin or metabolic enzymes, during fast-to-slow transformation in rabbit skeletal muscle cell culture. J Physiol 533: 215-226, 2001. (Pubitemid 32499373)
30. Meissner JD, Kubis HP, Scheibe RJ, Gros G. Reversible Ca2+-induced fast-to-slow transition in primary skeletal muscle culture cells at the mRNA level. J Physiol 523: 19-28, 2000. (Pubitemid 30135818)
31. Meissner JD, Umeda PK, Chang KC, Gros G, Scheibe RJ. Activation of the beta myosin heavy chain promoter by MEF-2D, MyoD, p300, and the calcineurin/NFATc1 pathway. J Cell Physiol 211: 138-148, 2007. (Pubitemid 46363903)
32. Murgia M, Serrano AL, Calabria E, Pallafacchina G, Lomo T, Schiaffino S. Ras is involved in nerve-activity-dependent regulation of muscle genes. Nat Cell Biol 2: 142-147, 2000. (Pubitemid 30781128)
33. Olson EN, Spizz G, Tainsky MA. The oncogenic forms of N-ras or H-ras prevent skeletal myoblast differentiation. Mol Cell Biol 7: 2104-2111, 1987.
34. Perry RL, Parker MH, Rudnicki MA. Activated MEK1 binds the nuclear MyoD transcriptional complex to repress transactivation. Mol Cell 8: 291-301, 2001.
35. Pette D, Staron RS. Transitions of muscle fibre phenotypic profiles. Histochem Cell Biol 115: 359-372, 2001. (Pubitemid 32467749)
36. Puri PL, Sartorelli V. Regulation of muscle regulatory factors by DNA-binding, interacting proteins, and post-transcriptional modifications. J Cell Physiol 185: 155-173, 2000. (Pubitemid 30740357)
37. Rommel C, Clarke BA, Zimmermann S, Nunez L, Rossman R, Reid K, Moelling K, Yancopoulos GD, Glass DJ. Differentiation stage-specific inhibition of the Raf-MEK-ERK pathway by Akt. Science 286: 1738-1741, 1999. (Pubitemid 129515881)
38. Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning. New York: Cold Spring Harbor Laboratory, 1989.
39. Shi X, Garry DJ. Muscle stem cells in development, regeneration, and disease. Genes Dev 20: 1692-1708, 2006. (Pubitemid 43992877)
40. Tamir Y, Bengal E. Phosphoinositide 3-kinase induces the transcriptional activity of MEF2 proteins during muscle differentiation. J Biol Chem 275: 34424-34432, 2000. (Pubitemid 30819213)
41. Umeda PK, Levin JE, Sinha AM, Cribbs LL, Darling DS, Ende DJ, Hsu HJ, Dizon E, Jakovcic S. Molecular Biology of Muscle Development. New York: Liss, 1986.
42. Wu Z, Woodring PJ, Bhakta KS, Tamura K, Wen F, Feramisco JR, Karin M, Wang JY, Puri PL. p38 and extracellular signal-regulated kinases regulate the myogenic program at multiple steps. Mol Cell Biol 20: 3951-3964, 2000. (Pubitemid 30314494)
43. Zimmermann S, Moelling K. Phosphorylation and regulation of Raf by Akt (protein kinase B). Science 286: 1741-1744, 1999. (Pubitemid 129515882)