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PMID: 7818554 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Regulation of cyclins and p34CDC2 expression during terminal differentiation of C2C12 myocytes.

Biochemical and biophysical research communications ·Vol. 206 ·No. 1 ·1995-01-05 ·Pages 82-8

Wang J, Nadal-Ginard B

Abstract

Little is known about the expression of cell cycle regulatory genes upon terminal differentiation of skeletal muscle cells. In this report, we demonstrate that the expressions of cyclin A, cyclin D1 and p34cdc2 are downregulated upon C2C12 myocytes differentiation and are not inducible in differentiated myotubes. SV40 large T antigen can induce cell cycle entry of myotubes through its induction of these genes' expressions and pRB phosphorylation as well as its suppression of Rb expression. These results provide the first direct evidence that the irreversible downregulation of cyclins and cyclin-dependent kinases is one mechanism for the permanent cell cycle withdrawal of myotubes.

MeSH Terms
Animals Antigens, Polyomavirus Transforming/biosynthesis Blotting, Northern CDC2 Protein Kinase/biosynthesis Cell Cycle Cell Differentiation Cell Line Cyclins/biosynthesis Gene Expression Regulation Immunoblotting Kinetics Mice Muscles/cytology,metabolism Protamine Kinase/metabolism RNA, Messenger/biosynthesis Retinoblastoma Protein/biosynthesis
Chemicals
Antigens, Polyomavirus Transforming Cyclins RNA, Messenger Retinoblastoma Protein Protamine Kinase CDC2 Protein Kinase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wang J
Department of Cardiology, Children's Hospital, Boston, Massachusetts 02115.
Nadal-Ginard B
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1995-01-05
Pages
82-8
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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