Protein acetylation: more than chromatin modification to regulate transcription
被引:24
作者:
Bayle, JH
论文数: 0引用数: 0
h-index: 0
机构:Stanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr Mol & Genet Med,Dept Pathol, Palo Alto, CA 94305 USA
Bayle, JH
Crabtree, GR
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr Mol & Genet Med,Dept Pathol, Palo Alto, CA 94305 USAStanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr Mol & Genet Med,Dept Pathol, Palo Alto, CA 94305 USA
Crabtree, GR
[1
]
机构:
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr Mol & Genet Med,Dept Pathol, Palo Alto, CA 94305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr Mol & Genet Med,Dept Dev Biol, Palo Alto, CA 94305 USA
来源:
CHEMISTRY & BIOLOGY
|
1997年
/
4卷
/
12期
关键词:
D O I:
10.1016/S1074-5521(97)90296-9
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:
Histone acetyltransferases and deacetylases are involved In the regulation of gene transcription. Recently, tumor suppressor protein p53 has been shown to be a target for transcriptional coactivators that have histone acetyltransferase activity, suggesting acetylation is also involved in the regulation of cell proliferation and tumorigenesis.