Transcriptional activation by nuclear receptors

被引:38
作者
Acevedo, ML [1 ]
Kraus, WL [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
来源
ESSAYS IN BIOCHEMISTRY: NUCLEAR RECEPTOR SUPERFAMILY | 2004年 / 40卷
关键词
D O I
10.1042/bse0400073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Transcriptional activation by nuclear receptors (NRs) involves the recruitment of distinct classes of co-activators and other transcription-related factors to target promoters in the chromatin environment of the nucleus. Chromatin has a general repressive effect on transcription, but also provides opportunities for NRs to regulate transcription by directing specific patterns of chromatin remodelling and histone modification. Ultimately, the transcription of hormone-regulated genes by NRs is critically dependent on co-ordinated physical and functional interactions among the receptors, chromatin, co-activators with chromatin-, historic- and factor-modifying activities, and the RNA polymerase II transcriptional machinery. In addition, several mechanisms exist to terminate or attenuate NR-dependent signalling, including modification, recycling, subcellular redistribution and degradation of the receptors or their associated cofactors. The complexity of NR-dependent transcription provides multiple targets for regulatory inputs, thus allowing each hormone-responsive cell to direct its transcriptional output in a physiologically appropriate manner.
引用
收藏
页码:73 / 88
页数:16
相关论文
共 35 条
[1]
Mediator and p300/CBP-steroid receptor coactivator complexes have distinct roles, but function synergistically, during estrogen receptor α-dependent transcription with chromatin templates [J].
Acevedo, ML ;
Kraus, WL .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :335-348
[2]
TAFs revisited: more data reveal new twists and confirm old ideas [J].
Albright, SR ;
Tjian, R .
GENE, 2000, 242 (1-2) :1-13
[3]
Coordinate regulation of transcription and splicing by steroid receptor coregulators [J].
Auboeuf, D ;
Hönig, A ;
Berget, SM ;
O'Malley, BW .
SCIENCE, 2002, 298 (5592) :416-419
[4]
The RNA polymerase II core promoter: a key component in the regulation of gene expression [J].
Butler, JEF ;
Kadonaga, JT .
GENES & DEVELOPMENT, 2002, 16 (20) :2583-2592
[5]
Regulation of hormone-induced histone hyperacetylation and gene activation via acetylation of an acetylase [J].
Chen, HW ;
Lin, RJ ;
Xie, W ;
Wilpitz, D ;
Evans, RM .
CELL, 1999, 98 (05) :675-686
[6]
Thyroid hormone, T3-dependent phosphorylation and translocation of Trip230 from the Golgi complex to the nucleus [J].
Chen, YM ;
Chen, PL ;
Chen, CF ;
Sharp, ZD ;
Lee, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4443-4448
[7]
Ordered recruitment: Gene-specific mechanism of transcription activation [J].
Cosma, MP .
MOLECULAR CELL, 2002, 10 (02) :227-236
[8]
Curtis SH, 2000, ADV PHARMACOL, V47, P357
[9]
Importance of the regulation of nuclear receptor degradation [J].
Dennis, AP ;
Haq, RU ;
Nawaz, Z .
FRONTIERS IN BIOSCIENCE, 2001, 6 :D954-D959
[10]
Nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription [J].
Dilworth, FJ ;
Chambon, P .
ONCOGENE, 2001, 20 (24) :3047-3054