Selective requirements for histone H3 and H4N termini in p300-dependent transcriptional activation from chromatin

被引:85
作者
An, WJ
Palhan, VB
Karymov, MA
Leuba, SH
Roeder, RG [1 ]
机构
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[2] NCI, Lab Receptor Biol & Gene Express, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(02)00497-5
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
The N-terminal tails of the core histones play important roles in transcriptional regulation, but their mechanism(s) of action are poorly understood. Here, pure chromatin templates assembled with varied combinations of recombinant wild-type and mutant core histones have been employed to ascertain the role of individual histone tails, both in overall acetylation patterns and in transcription. In vitro assays show an indispensable role for H3 and H4 tails, especially major lysine substrates, in p300-dependent transcriptional activation, as well as activator-targeted acetylation of promoter-proximal histone tails by p300. These results indicate, first, that constraints to transcription are imposed by nucleosomal histone components other than histone N-terminal tails and, second, that the histone N-terminal tails have selective roles, which can be modulated by targeted acetylation, in transcriptional activation by p300.
引用
收藏
页码:811 / 821
页数:11
相关论文
共 63 条
[31]   Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo [J].
Kuo, MH ;
Zhou, JX ;
Jambeck, P ;
Churchill, MEA ;
Allis, CD .
GENES & DEVELOPMENT, 1998, 12 (05) :627-639
[32]   Gcn4 activator targets Gcn5 histone acetyltransferase to specific promoters independently of transcription [J].
Kuo, MH ;
vom Baur, E ;
Struhl, K ;
Allis, CD .
MOLECULAR CELL, 2000, 6 (06) :1309-1320
[33]   HATs off: Selective synthetic inhibitors of the histone acetyltransferases p300 and PCAF [J].
Lau, OD ;
Kundu, TK ;
Soccio, RE ;
Ait-Si-Ali, S ;
Khalil, EM ;
Vassilev, A ;
Wolffe, AP ;
Nakatani, Y ;
Roeder, RG ;
Cole, PA .
MOLECULAR CELL, 2000, 5 (03) :589-595
[34]   A POSITIVE ROLE FOR HISTONE ACETYLATION IN TRANSCRIPTION FACTOR ACCESS TO NUCLEOSOMAL DNA [J].
LEE, DY ;
HAYES, JJ ;
PRUSS, D ;
WOLFFE, AP .
CELL, 1993, 72 (01) :73-84
[35]   Binding of retinoic acid receptor heterodimers to DNA -: A role for histones NH2 termini [J].
Lefebvre, P ;
Mouchon, A ;
Lefebvre, B ;
Formstecher, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :12288-12295
[36]   All four core histone N-termini contain sequences required for the repression of basal transcription in yeast [J].
Lenfant, F ;
Mann, RK ;
Thomsen, B ;
Ling, XF ;
Grunstein, M .
EMBO JOURNAL, 1996, 15 (15) :3974-3985
[37]   Biochemical analysis of chromatin containing recombinant Drosophila core histones [J].
Levenstein, ME ;
Kadonaga, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8749-8754
[38]  
Loyola A, 2001, GENE DEV, V15, P2837
[39]   Characterization of nucleosome core particles containing histone proteins made in bacteria [J].
Luger, K ;
Rechsteiner, TJ ;
Flaus, AJ ;
Waye, MMY ;
Richmond, TJ .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 272 (03) :301-311
[40]   Crystal structure of the nucleosome core particle at 2.8 angstrom resolution [J].
Luger, K ;
Mader, AW ;
Richmond, RK ;
Sargent, DF ;
Richmond, TJ .
NATURE, 1997, 389 (6648) :251-260