Post-mitotic role of nucleostemin as a promoter of skeletal muscle cell differentiation

Biochemical and Biophysical Research Communications

Volumn 391, Issue 1, 2010, Pages 299-304

  Hirai, Hiroyuki ^a   Romanova, Liudmila ^a   Kellner, Steven ^a   Verma, Mayank ^a   Rayner, Samuel ^a   Asakura, Atsushi ^a   Kikyo, Nobuaki ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

Myogenesis; Nucleostemin; p53; Protein synthesis

Indexed keywords

MYOD PROTEIN; MYOGENIN; NUCLEOLIN; NUCLEOSTEMIN; PROTEIN P53; RIBOSOME RNA; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL CYCLE REGULATION; CELL DIFFERENTIATION; CELL PROLIFERATION; DOWN REGULATION; FLUORESCENCE ACTIVATED CELL SORTING; MITOSIS; MOUSE; MYOBLAST; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA PROCESSING; SATELLITE CELL; SKELETAL MUSCLE; STEM CELL; TISSUE REGENERATION; UPREGULATION;

ANIMALS; CARRIER PROTEINS; CELL DIFFERENTIATION; GENE KNOCKDOWN TECHNIQUES; MICE; MICE, MUTANT STRAINS; MITOSIS; MUSCLE DEVELOPMENT; MUSCLE, SKELETAL; NUCLEAR PROTEINS; SATELLITE CELLS, SKELETAL MUSCLE; TUMOR SUPPRESSOR PROTEIN P53;

EID: 72949113005     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.11.053     Document Type: Article

References (26)

1. Ma H., and Pederson T. Nucleostemin: a multiplex regulator of cell-cycle progression. Trends Cell Biol. 18 (2008) 575-579
2. Tsai R.Y., and McKay R.D. A nucleolar mechanism controlling cell proliferation in stem cells and cancer cells. Genes Dev. 16 (2002) 2991-3003
3. Siddiqi S., Gude N., Hosoda T., Muraski J., Rubio M., Emmanuel G., Fransioli J., Vitale S., Parolin C., D'Amario D., Schaefer E., Kajstura J., Leri A., Anversa P., and Sussman M.A. Myocardial induction of nucleostemin in response to postnatal growth and pathological challenge. Circ. Res. 103 (2008) 89-97
4. Kafienah W., Mistry S., Williams C., and Hollander A.P. Nucleostemin is a marker of proliferating stromal stem cells in adult human bone marrow. Stem Cells 24 (2006) 1113-1120
5. Maki N., Takechi K., Sano S., Tarui H., Sasai Y., and Agata K. Rapid accumulation of nucleostemin in nucleolus during newt regeneration. Dev. Dyn. 236 (2007) 941-950
6. Romanova L., Grand A., Zhang L., Rayner S., Katoku-Kikyo N., Kellner S., and Kikyo N. Critical role of nucleostemin in pre-rRNA processing. J. Biol. Chem. 284 (2009) 4968-4977
7. Charge S.B., and Rudnicki M.A. Cellular and molecular regulation of muscle regeneration. Physiol. Rev. 84 (2004) 209-238
8. Orcutt M.W., and Young R.B. Cell differentiation, protein synthesis rate and protein accumulation in muscle cell cultures isolated from embryos of layer and broiler chickens. J. Anim. Sci. 54 (1982) 769-776
9. Plaisance I., Morandi C., Murigande C., and Brink M. TNF-alpha increases protein content in C2C12 and primary myotubes by enhancing protein translation via the TNF-R1, PI3K, and MEK. Am. J. Physiol. Endocrinol. Metab. 294 (2008) E241-E250
10. Asakura A., Komaki M., and Rudnicki M. Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation. Differentiation 68 (2001) 245-253
11. Beauchamp J.R., Heslop L., Yu D.S., Tajbakhsh S., Kelly R.G., Wernig A., Buckingham M.E., Partridge T.A., and Zammit P.S. Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells. J. Cell Biol. 151 (2000) 1221-1234
12. Asakura A., Seale P., Girgis-Gabardo A., and Rudnicki M.A. Myogenic specification of side population cells in skeletal muscle. J. Cell Biol. 159 (2002) 123-134
13. Kuang S., Kuroda K., Le Grand F., and Rudnicki M.A. Asymmetric self-renewal and commitment of satellite stem cells in muscle. Cell 129 (2007) 999-1010
14. Kitamura T., Koshino Y., Shibata F., Oki T., Nakajima H., Nosaka T., and Kumagai H. Retrovirus-mediated gene transfer and expression cloning: powerful tools in functional genomics. Exp. Hematol. 31 (2003) 1007-1014
15. Morita S., Kojima T., and Kitamura T. Plat-E: an efficient and stable system for transient packaging of retroviruses. Gene Ther. 7 (2000) 1063-1066
16. Gussoni E., Soneoka Y., Strickland C.D., Buzney E.A., Khan M.K., Flint A.F., Kunkel L.M., and Mulligan R.C. Dystrophin expression in the mdx mouse restored by stem cell transplantation. Nature 401 (1999) 390-394
17. Rosser B.W., Dean M.S., and Bandman E. Myonuclear domain size varies along the lengths of maturing skeletal muscle fibers. Int. J. Dev. Biol. 46 (2002) 747-754
18. Seale P., Sabourin L.A., Girgis-Gabardo A., Mansouri A., Gruss P., and Rudnicki M.A. Pax7 is required for the specification of myogenic satellite cells. Cell 102 (2000) 777-786
19. Sacco A., Doyonnas R., Kraft P., Vitorovic S., and Blau H.M. Self-renewal and expansion of single transplanted muscle stem cells. Nature 456 (2008) 502-506
20. Olson E.N., and Klein W.H. BHLH factors in muscle development: dead lines and commitments, what to leave in and what to leave out. Genes Dev. 8 (1994) 1-8
21. Thayer M.J., Tapscott S.J., Davis R.L., Wright W.E., Lassar A.B., and Weintraub H. Positive autoregulation of the myogenic determination gene MyoD1. Cell 58 (1989) 241-248
22. Edmondson D.G., Brennan T.J., and Olson E.N. Mitogenic repression of myogenin autoregulation. J. Biol. Chem. 266 (1991) 21343-21346
23. Wright W.E., Sassoon D.A., and Lin V.K. Myogenin, a factor regulating myogenesis, has a domain homologous to MyoD. Cell 56 (1989) 607-617
24. Dai M.S., Sun X.X., and Lu H. Aberrant expression of nucleostemin activates p53 and induces cell cycle arrest via inhibition of MDM2. Mol. Cell Biol. 28 (2008) 4365-4376
25. Schwarzkopf M., Coletti D., Sassoon D., and Marazzi G. Muscle cachexia is regulated by a p53-PW1/Peg3-dependent pathway. Genes Dev. 20 (2006) 3440-3452
26. Kitzmann M., and Fernandez A. Crosstalk between cell cycle regulators and the myogenic factor MyoD in skeletal myoblasts. Cell. Mol. Life Sci. 58 (2001) 571-579