A feedback circuit between miR-133 and the ERK1/2 pathway involving an exquisite mechanism for regulating myoblast proliferation and differentiation

Cell Death and Disease

Volumn 4, Issue 11, 2013, Pages

  Feng, Y ^a,b   Niu, L L ^a   Wei, W ^a   Zhang, W Y ^a   Li, X Y ^a   Cao, J H ^a   Zhao, S H ^a  

^a HUAZHONG AGRICULTURAL UNIVERSITY   (China)

^b KUNMING UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Differentiation; ERK1 2; FGFR1; miR 133; Myoblast; PP2AC

Indexed keywords

MICRORNA; MICRORNA 133; MICRORNA 133A; MICRORNA 133B; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; UNCLASSIFIED DRUG;

ARTICLE; CELL DIFFERENTIATION; CELL PROLIFERATION; DOWN REGULATION; ENZYME ACTIVITY; FEEDBACK SYSTEM; MUSCLE DEVELOPMENT; MYOBLAST; MYOTUBE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; UPREGULATION;

ANIMALS; BLOTTING, WESTERN; CELL CYCLE; CELL DIFFERENTIATION; CELL PROLIFERATION; MAP KINASE SIGNALING SYSTEM; MICE; MICRORNAS; MYOBLASTS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 84889579981     PISSN: None     EISSN: 20414889     Source Type: Journal    
DOI: 10.1038/cddis.2013.462     Document Type: Article

References (44)

1. Bartel DP. MicroRNAs: Genomics, biogenesis, mechanism, and function. Cell 2004; 116: 281-297
2. Sun W, Julie Li YS, Huang HD, Shyy JY, Chien S. MicroRNA: A master regulator of cellular processes for bioengineering systems. Annu Rev Biomed Eng 2010; 12: 1-27
3. Wightman B, Ha I, Ruvkun G. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell 1993; 75: 855-862
4. Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell 1993; 75: 843-854
5. Stefani G, Slack FJ. Small non-coding RNAs in animal development. Nat Rev Mol Cell Biol 2008; 9: 219-230
6. Sokol NS, Ambros V. Mesodermally expressed Drosophila microRNA-1 is regulated by Twist and is required in muscles during larval growth. Genes Dev 2005; 19: 2343-2354
7. Chen JF, Mandel EM, Thomson JM, Wu Q, Callis TE, Hammond SM, et al. The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation. Nat Genet 2006; 38: 228-233
8. Kim HK, Lee YS, Sivaprasad U, Malhotra A, Dutta A. Muscle-specific microRNA miR-206 promotes muscle differentiation. J Cell Biol 2006; 174: 677-687
9. Anderson C, Catoe H, Werner R. MIR-206 regulates connexin43 expression during skeletal muscle development. Nucleic Acids Res 2006; 34: 5863-5871
10. Naguibneva I, Ameyar-Zazoua M, Polesskaya A, Ait-Si-Ali S, Groisman R, Souidi M, et al. The microRNA miR-181 targets the homeobox protein Hox-A11 during mammalian myoblast differentiation. Nat Cell Biol 2006; 8: 278-284
11. Sun Q, Zhang Y, Yang G, Chen X, Cao G, Wang J, et al. Transforming growth factor-betaregulated miR-24 promotes skeletal muscle differentiation. Nucleic Acids Res 2008; 36: 2690-2699
12. Wong CF, Tellam RL. MicroRNA-26a targets the histone methyltransferase Enhancer of Zeste homolog 2 during myogenesis. J Biol Chem 2008; 283: 9836-9843
13. Wang H, Garzon R, Sun H, Ladner KJ, Singh R, Dahlman J, et al. NF-kappaB-YY1-miR-29 regulatory circuitry in skeletal myogenesis and rhabdomyosarcoma. Cancer Cell 2008; 14: 369-381
14. Mishima Y, Abreu-Goodger C, Staton AA, Stahlhut C, Shou C, Cheng C, et al. Zebrafish miR-1 and miR-133 shape muscle gene expression and regulate sarcomeric actin organization. Genes Dev 2009; 23: 619-632
15. Zhang D, Li XH, Chen CC, Li YY, Lei Z, Jing YY, et al. Attenuation of p38-mediated miR-1/133 Expression Facilitates Myoblast Proliferation during the Early Stage of Muscle Regeneration. PLoS One 2012; 7: E41478
16. Campbell JS, Wenderoth MP, Hauschka SD, Krebs EG. Differential activation of mitogenactivated protein kinase in response to basic fibroblast growth factor in skeletal muscle cells. Proc Natl Acad Sci USA 1995; 92: 870-874
17. Janssens V, Goris J. Protein phosphatase 2A: A highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling. Biochem J 2001; 353(Part 3): 417-439
18. Pearson G, Robinson F, Beers Gibson T, Xu BE, Karandikar M, Berman K, et al. Mitogen-Activated protein (MAP) kinase pathways: Regulation and physiological functions. Endocr Rev 2001; 22: 153-183
19. Bennett AM, Tonks NK. Regulation of distinct stages of skeletal muscle differentiation by mitogen-Activated protein kinases. Science 1997; 278: 1288-1291
20. Yang W, Chen Y, Zhang Y, Wang X, Yang N, Zhu D. Extracellular signal-regulated kinase 1/2 mitogen-Activated protein kinase pathway is involved in myostatin-regulated differentiation repression. Cancer Res 2006; 66: 1320-1326
21. Yaffe D, Saxel O. Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle. Nature 1977; 270: 725-727
22. Huang TH, Zhu MJ, Li XY, Zhao SH. Discovery of porcine microRNAs and profiling from skeletal muscle tissues during development. PLoS One 2008; 3: E3225
23. Mitchell P, Steenstrup T, Hannon K. Expression of fibroblast growth factor family during postnatal skeletal muscle hypertrophy. J Appl Physiol 1999; 86: 313-319
24. Sheehan SM, Allen RE. Skeletal muscle satellite cell proliferation in response to members of the fibroblast growth factor family and hepatocyte growth factor. J Cell Physiol 1999; 181: 499-506
25. Martelly I, Soulet L, Bonnavaud S, Cebrian J, Gautron J, Barritault D. Differential expression of FGF receptors and of myogenic regulatory factors in primary cultures of satellite cells originating from fast (EDL) and slow (Soleus) twitch rat muscles. Cell Mol Biol (Noisy-le-Grand) 2000; 46: 1239-1248
26. Templeton TJ, Hauschka SD. FGF-mediated aspects of skeletal muscle growth and differentiation are controlled by a high affinity receptor, FGFR1. Dev Biol 1992; 154: 169-181
27. Scata KA, Bernard DW, Fox J, Swain JL. FGF receptor availability regulates skeletal myogenesis. Exp Cell Res 1999; 250: 10-21
28. Belevych AE, Sansom SE, Terentyeva R, Ho HT, Nishijima Y, Martin MM, et al. MicroRNA-1 and-133 increase arrhythmogenesis in heart failure by dissociating phosphatase activity from RyR2 complex. PLoS One 6: E28324
29. Weyman CM, Wolfman A. Mitogen-Activated protein kinase kinase (MEK) activity is required for inhibition of skeletal muscle differentiation by insulin-like growth factor 1 or fibroblast growth factor 2. Endocrinology 1998; 139: 1794-1800
30. Jones NC, Fedorov YV, Rosenthal RS, Olwin BB. ERK1/2 is required for myoblast proliferation but is dispensable for muscle gene expression and cell fusion. J Cell Physiol 2001; 186: 104-115
31. Milasincic DJ, Calera MR, Farmer SR, Pilch PF. Stimulation of C2C12 myoblast growth by basic fibroblast growth factor and insulin-like growth factor 1 can occur via mitogenactivated protein kinase-dependent and-independent pathways. Mol Cell Biol 1996; 16: 5964-5973
32. Miralles F, Ron D, Baiget M, Felez J, Munoz-Canoves P. Differential regulation of urokinase-Type plasminogen activator expression by basic fibroblast growth factor and serum in myogenesis. Requirement of a common mitogen-Activated protein kinase pathway. J Biol Chem 1998; 273: 2052-2058
33. de Alvaro C, Martinez N, Rojas JM, Lorenzo M. Sprouty-2 overexpression in C2C12 cells confers myogenic differentiation properties in the presence of FGF2. Mol Biol Cell 2005; 16: 4454-4461
34. Abraham D, Podar K, Pacher M, Kubicek M, Welzel N, Hemmings BA, et al. Raf-1-Associated protein phosphatase 2A as a positive regulator of kinase activation. J Biol Chem 2000; 275: 22300-22304
35. Ory S, Zhou M, Conrads TP, Veenstra TD, Morrison DK. Protein phosphatase 2A positively regulates Ras signaling by dephosphorylating KSR1 and Raf-1 on critical 14-3-3 binding sites. Curr Biol 2003; 13: 1356-1364
36. Jaumot M, Hancock JF. Protein phosphatases 1 and 2A promote Raf-1 activation by regulating 14-3-3 interactions. Oncogene 2001; 20: 3949-3958
37. Kubicek M, Pacher M, Abraham D, Podar K, Eulitz M, Baccarini M. Dephosphorylation of Ser-259 regulates Raf-1 membrane association. J Biol Chem 2002; 277: 7913-7919
38. Adams DG, Coffee RL Jr, Zhang H, Pelech S, Strack S, Wadzinski BE. Positive regulation of Raf1-MEK1/2-ERK1/2 signaling by protein serine/threonine phosphatase 2A holoenzymes. J Biol Chem 2005; 280: 42644-42654
39. Flanagan-Steet H, Hannon K, McAvoy MJ, Hullinger R, Olwin BB. Loss of FGF receptor 1 signaling reduces skeletal muscle mass and disrupts myofiber organization in the developing limb. Dev Biol 2000; 218: 21-37
40. Li J, Johnson SE. ERK2 is required for efficient terminal differentiation of skeletal myoblasts. Biochem Biophys Res Commun 2006; 345: 1425-1433
41. Bischoff R, Holtzer H. Mitosis and the processes of differentiation of myogenic cells in vitro. J Cell Biol 1969; 41: 188-200
42. Xie SS, Li XY, Liu T, Cao JH, Zhong Q, Zhao SH. Discovery of porcine microRNAs in multiple tissues by a Solexa deep sequencing approach. PLoS One 2011; 6: E16235
43. Chen C, Ridzon DA, Broomer AJ, Zhou Z, Lee DH, Nguyen JT, et al. Real-Time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res 2005; 33: E179
44. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-Time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 2001; 25: 402-408