CBP/p300 and muscle differentiation: no HAT, no muscle

被引:99
作者
Polesskaya, A
Naguibneva, I
Fritsch, L
Duquet, A
Ait-Si-Ali, S
Robin, R
Vervisch, A
Pritchard, LL
Cole, P
Harel-Bellan, A
机构
[1] CNRS, UPR 9079, F-94800 Villejuif, France
[2] Inst Andre Lwoff, Serv Cytofluorometrie, F-94800 Villejuif, France
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
关键词
CREB-binding protein (CBP); histone acetyltransferase; MyoD; myogenesis; p300;
D O I
10.1093/emboj/20.23.6816
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
Terminal differentiation of muscle cells follows a precisely orchestrated program of transcriptional regulatory events at the promoters of both muscle-specific and ubiquitous genes. Two distinct families of transcriptional co-activators, GCN5/PCAF and CREB-binding protein (CBP)/p300, are crucial to this process. While both possess histone acetyl-transferase (HAT) activity, previous studies have failed to identify a requirement for CBP/p300 HAT function in myogenic differentiation. We have addressed this issue directly using a chemical inhibitor of CBP/p300 in addition to a negative transdominant mutant. Our results clearly demonstrate that CBP/p300 HAT activity is critical for myogenic terminal differentiation. Furthermore, this requirement is restricted to a subset of events in the differentiation program: cell fusion and specific gene expression. These data help to define the requirements for enzymatic function of distinct coactivators at different stages of the muscle cell differentiation program.
引用
收藏
页码:6816 / 6825
页数:10
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