MyoD can induce cell cycle arrest but not muscle differentiation in the presence of dominant negative SWI/SNF chromatin remodeling enzymes

被引:95
作者
de la Serna, IL [1 ]
Roy, K [1 ]
Carlson, KA [1 ]
Imbalzano, AN [1 ]
机构
[1] Univ Massachusetts, Dept Cell Biol, Sch Med, Worcester, MA 01655 USA
关键词
D O I
10.1074/jbc.M107281200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell cycle arrest is critical for muscle differentiation, and the two processes are closely coordinated but temporally separable. SWI/SNF complexes are ATP-dependent chromatin-remodeling enzymes that have been shown to be required for muscle differentiation in cell culture and have also been reported to be required for Rb-mediated cell cycle arrest. We therefore looked more closely at how SWI/SNF enzymes affect the events that occur during MyoD-induced myogenesis, namely, cell cycle regulation and muscle-specific gene expression, in cells that inducibly express dominant negative versions of Brahma (BRM) and Brahma-related gene 1 (BRG1), the ATPase subunits of two distinct SWI/SNF complexes. Although dominant negative BRM and BRG1 inhibited expression of every muscle-specific regulator and structural gene assayed, there was no effect on MyoD-induced activation of cell cycle regulatory proteins, and thus, cells arrested normally. In particular, in the presence or absence of dominant negative BRM or BRG1, MyoD was able to activate expression of p21, cyclin D3, and Rb, all of which are critical for cell cycle withdrawal in the G(1)/G(0) phase of the cell cycle. These findings suggest that at least one basis for the distinct mechanisms that regulate cessation of cell proliferation and muscle-specific gene expression during muscle differentiation is that SWI/SNF-mediated chromatin-remodeling enzymes are required only for the latter.
引用
收藏
页码:41486 / 41491
页数:6
相关论文
共 65 条
[1]   Ordered recruitment of chromatin modifying and general transcription factors to the IFN-β promoter [J].
Agalioti, T ;
Lomvardas, S ;
Parekh, B ;
Yie, JM ;
Maniatis, T ;
Thanos, D .
CELL, 2000, 103 (04) :667-678
[2]   Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis [J].
Andres, V ;
Walsh, K .
JOURNAL OF CELL BIOLOGY, 1996, 132 (04) :657-666
[3]   A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro [J].
Armstrong, JA ;
Bieker, JJ ;
Emerson, BM .
CELL, 1998, 95 (01) :93-104
[4]   DIFFERENCES AND SIMILARITIES IN DNA-BINDING PREFERENCES OF MYOD AND E2A PROTEIN COMPLEXES REVEALED BY BINDING-SITE SELECTION [J].
BLACKWELL, TK ;
WEINTRAUB, H .
SCIENCE, 1990, 250 (4984) :1104-1110
[5]   TARGETED INACTIVATION OF THE MUSCLE REGULATORY GENE MYF-5 RESULTS IN ABNORMAL RIB DEVELOPMENT AND PERINATAL DEATH [J].
BRAUN, T ;
RUDNICKI, MA ;
ARNOLD, HH ;
JAENISCH, R .
CELL, 1992, 71 (03) :369-382
[6]   INACTIVATION OF MYF-6 AND MYF-5 GENES IN MICE LEADS TO ALTERATIONS IN SKELETAL-MUSCLE DEVELOPMENT [J].
BRAUN, T ;
ARNOLD, HH .
EMBO JOURNAL, 1995, 14 (06) :1176-1186
[7]   Activator-dependent regulation of transcriptional pausing on nucleosomal templates [J].
Brown, SA ;
Imbalzano, AN ;
Kingston, RE .
GENES & DEVELOPMENT, 1996, 10 (12) :1479-1490
[8]   MAKING MUSCLE IN MAMMALS [J].
BUCKINGHAM, M .
TRENDS IN GENETICS, 1992, 8 (04) :144-149
[9]  
Cenciarelli C, 1999, MOL CELL BIOL, V19, P5203
[10]   c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for transactivation function [J].
Cheng, SWG ;
Davies, KP ;
Yung, E ;
Beltran, RJ ;
Yu, J ;
Kalpana, GV .
NATURE GENETICS, 1999, 22 (01) :102-105