Publication Date:
1995-02-17
Description:
Skeletal muscle differentiation entails the coordination of muscle-specific gene expression and terminal withdrawal from the cell cycle. This cell cycle arrest in the G0 phase requires the retinoblastoma tumor suppressor protein (Rb). The function of Rb is negatively regulated by cyclin-dependent kinases (Cdks), which are controlled by Cdk inhibitors. Expression of MyoD, a skeletal muscle-specific transcriptional regulator, activated the expression of the Cdk inhibitor p21 during differentiation of murine myocytes and in nonmyogenic cells. MyoD-mediated induction of p21 did not require the tumor suppressor protein p53 and correlated with cell cycle withdrawal. Thus, MyoD may induce terminal cell cycle arrest during skeletal muscle differentiation by increasing the expression of p21.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Halevy, O -- Novitch, B G -- Spicer, D B -- Skapek, S X -- Rhee, J -- Hannon, G J -- Beach, D -- Lassar, A B -- F32ARO8214-01A1/AR/NIAMS NIH HHS/ -- N01-HD-6-2915/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1995 Feb 17;267(5200):1018-21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7863327" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
*Carrier Proteins
;
*Cell Cycle
;
*Cell Cycle Proteins
;
*Cell Differentiation
;
Cell Line
;
Cyclin-Dependent Kinase Inhibitor p21
;
Cyclin-Dependent Kinase Inhibitor p27
;
Cyclin-Dependent Kinases/*antagonists & inhibitors
;
Cyclins/*biosynthesis/genetics
;
*DNA-Binding Proteins
;
E2F Transcription Factors
;
G0 Phase
;
Humans
;
Mice
;
Microtubule-Associated Proteins/biosynthesis/genetics
;
Muscle, Skeletal/*cytology/metabolism
;
MyoD Protein/*physiology
;
RNA, Messenger/genetics/metabolism
;
Retinoblastoma Protein/physiology
;
Retinoblastoma-Binding Protein 1
;
Transcription Factor DP1
;
Transcription Factors/metabolism
;
Tumor Cells, Cultured
;
Tumor Suppressor Protein p53/physiology
;
*Tumor Suppressor Proteins
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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