ATP-dependent chromatin remodeling complexes and their role in nuclear receptor-dependent transcription in vivo

被引:23
作者
Aoyagi, S [1 ]
Trotter, KW [1 ]
Archer, TK [1 ]
机构
[1] NIEHS, Chromatin & Gene Express Sect, Mol Carcinogenesis Lab, NIH, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1016/S0083-6729(05)70009-1
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
Nuclear receptors (NRs) are ligand-dependent transcription factors that mediate transcription of target genes in chromatin. Modulation of chromatin structure plays an important part in the NR-mediated transcription process. ATP-dependent chromatin remodeling complexes have been shown to be intimately involved in NR-mediated transcription. In this review, we examine the role of chromatin remodeling complexes in facilitating the recruitment of coregulators and basal transcription factors. In addition, the role of subunit specificity within the chromatin remodeling complexes, the complexes' influence on remodeling activity, and complexes' recruitment to the NR-responsive promoters are discussed. (c) 2005 Elsevier Inc.
引用
收藏
页码:281 / 307
页数:27
相关论文
共 172 条
[1]   The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly [J].
Ahmad, K ;
Henikoff, S .
MOLECULAR CELL, 2002, 9 (06) :1191-1200
[2]   ISOLATION AND CHARACTERIZATION OF 2 HUMAN H1 HISTONE GENES WITHIN CLUSTERS OF CORE HISTONE GENES [J].
ALBIG, W ;
KARDALINOU, E ;
DRABENT, B ;
ZIMMER, A ;
DOENECKE, D .
GENOMICS, 1991, 10 (04) :940-948
[3]   Rad54 protein possesses chromatin-remodeling activity stimulated by the Rad51-ssDNA nucleoprotein filament [J].
Alexeev, A ;
Mazin, A ;
Kowalczykowski, SC .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (03) :182-186
[4]   ACETYLATION + METHYLATION OF HISTONES + THEIR POSSIBLE ROLE IN REGULATION OF RNA SYNTHESIS [J].
ALLFREY, VG ;
FAULKNER, R ;
MIRSKY, AE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1964, 51 (05) :786-+
[5]  
[Anonymous], [No title captured]
[6]   TRANSCRIPTION FACTOR ACCESS IS MEDIATED BY ACCURATELY POSITIONED NUCLEOSOMES ON THE MOUSE MAMMARY-TUMOR VIRUS PROMOTER [J].
ARCHER, TK ;
CORDINGLEY, MG ;
WOLFORD, RG ;
HAGER, GL .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :688-698
[7]   TRANSCRIPTION FACTOR LOADING ON THE MMTV PROMOTER - A BIMODAL MECHANISM FOR PROMOTER ACTIVATION [J].
ARCHER, TK ;
LEFEBVRE, P ;
WOLFORD, RG ;
HAGER, GL .
SCIENCE, 1992, 255 (5051) :1573-1576
[8]   THE HISTONE FOLD - A UBIQUITOUS ARCHITECTURAL MOTIF UTILIZED IN DNA COMPACTION AND PROTEIN DIMERIZATION [J].
ARENTS, G ;
MOUDRIANAKIS, EN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11170-11174
[9]   USE OF SELECTIVELY TRYPSINIZED NUCLEOSOME CORE PARTICLES TO ANALYZE THE ROLE OF THE HISTONE TAILS IN THE STABILIZATION OF THE NUCLEOSOME [J].
AUSIO, J ;
DONG, F ;
VANHOLDE, KE .
JOURNAL OF MOLECULAR BIOLOGY, 1989, 206 (03) :451-463
[10]   Hormone-mediated dephosphorylation of specific histone H1 isoforms [J].
Banks, GC ;
Deterding, LJ ;
Tomer, KB ;
Archer, TK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36467-36473