Transcriptional activation triggers deposition and removal of the histone variant H3.3

被引:250
作者
Schwartz, BE [1 ]
Ahmad, K [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
关键词
H3.3; nucleosome; chromatin; transcription; histone; Drosophila;
D O I
10.1101/gad.1259805
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DNA in eukaryotic cells is packaged into nucleosomes, the structural unit of chromatin. Both DNA and bulk histones are extremely long-lived, because old DNA strands and histones are retained when chromatin duplicates. In contrast, we find that the Drosophila HSP70 genes rapidly lose histone H3 and acquire variant H3.3 histones as they are induced. Histone replacement does not occur at artificial HSP70 promoter arrays, demonstrating that transcription is required for H3.3 deposition. The H3.3 histone is enriched in all active chromatin and throughout large transcription units, implying that deposition occurs during transcription elongation. Strikingly, we observed that the stability of chromatin-bound H3.3 differs between loci: H3.3 turns over at continually active rDNA genes, but becomes stable at induced HSP70 genes that have shut down. We conclude that H3.3 deposition is coupled to transcription, and continues while a gene is active. Repeated histone replacement suggests a mechanism to both maintain the structure of chromatin and access to DNA at active genes.
引用
收藏
页码:804 / 814
页数:11
相关论文
共 46 条
[1]   Chromatin disassembly mediated by the histone chaperone Asf1 is essential for transcriptional activation of the yeast PH05 and PH08 genes [J].
Adkins, MW ;
Howar, SR ;
Tyler, JK .
MOLECULAR CELL, 2004, 14 (05) :657-666
[2]   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
[3]   Centromeres are specialized replication domains in heterochromatin [J].
Ahmad, K ;
Henikoff, S .
JOURNAL OF CELL BIOLOGY, 2001, 153 (01) :101-109
[4]   Histone modification governs the cell cycle regulation of a replication-independent chromatin assembly pathway in Saccharomyces cerevisiae [J].
Altheim, BA ;
Schultz, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1345-1350
[5]   High-resolution localization of Drosophila Spt5 and Spt6 at heat shock genes in vivo:: roles in promoter proximal pausing and transcription elongation [J].
Andrulis, ED ;
Guzmán, E ;
Döring, P ;
Werner, J ;
Lis, JT .
GENES & DEVELOPMENT, 2000, 14 (20) :2635-2649
[6]   Nucleosomes unfold completely at a transcriptionally active promoter [J].
Boeger, H ;
Griesenbeck, J ;
Strattan, JS ;
Kornberg, RD .
MOLECULAR CELL, 2003, 11 (06) :1587-1598
[7]   A monomeric red fluorescent protein [J].
Campbell, RE ;
Tour, O ;
Palmer, AE ;
Steinbach, PA ;
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7877-7882
[8]   Proteolysis contributes to the exclusive centromere localization of the yeast Cse4/CENP-A histone H3 variant [J].
Collins, KA ;
Furuyama, S ;
Biggins, S .
CURRENT BIOLOGY, 2004, 14 (21) :1968-1972
[9]   STRUCTURE OF CHROMATIN AT DEOXYRIBONUCLEIC-ACID REPLICATION FORKS - NUCLEASE HYPERSENSITIVITY RESULTS FROM BOTH PRENUCLEOSOMAL DEOXYRIBONUCLEIC-ACID AND AN IMMATURE CHROMATIN STRUCTURE [J].
CUSICK, ME ;
LEE, KS ;
DEPAMPHILIS, ML ;
WASSARMAN, PM .
BIOCHEMISTRY, 1983, 22 (16) :3873-3884
[10]   Histones: Genetic diversity and tissue-specific gene expression [J].
Doenecke, D ;
Albig, W ;
Bode, C ;
Drabent, B ;
Franke, K ;
Gavenis, K ;
Witt, O .
HISTOCHEMISTRY AND CELL BIOLOGY, 1997, 107 (01) :1-10