Title The chromatin remodeling complex NuRD establishes the poised state of rRNA genes characterized by bivalent histone modifications and altered nucleosome positions
Authors Xie, Wenbing
Ling, Te
Zhou, Yonggang
Feng, Weijun
Zhu, Qiaoyun
Stunnenberg, Henk G.
Grummt, Ingrid
Tao, Wei
Affiliation German Canc Res Ctr, Div Mol Biol Cell 2, D-69120 Heidelberg, Germany.
Peking Univ, Key Lab Cell Proliferat & Differentiat, Educ Minist, Beijing 100871, Peoples R China.
Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands.
Keywords poised chromatin
cell differentiation
epigenetic dynamics
NoRC
POLYMERASE-I TRANSCRIPTION
NORC
BINDING
PROTEIN
METHYLTRANSFERASE
CHROMODOMAINS
METHYLATION
TERMINATION
EXPRESSION
MI-2-BETA
Issue Date 2012
Publisher proceedings of the national academy of sciences of the united states of america
Citation PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA.2012,109,(21),8161-8166.
Abstract rRNA genes (rDNA) exist in two distinct epigenetic states, active promoters being unmethylated and marked by euchromatic histone modifications, whereas silent ones are methylated and exhibit heterochromatic features. Here we show that the nucleosome remodeling and deacetylation (NuRD) complex establishes a specific chromatin structure at rRNA genes that are poised for transcription activation. The promoter of poised rRNA genes is unmethylated, associated with components of the preinitiation complex, marked by bivalent histone modifications and covered by a nucleosome in the "off" position, which is refractory to transcription initiation. Repression of rDNA transcription in growth-arrested and differentiated cells correlates with elevated association of NuRD and increased levels of poised rRNA genes. Reactivation of transcription requires resetting the promoter-bound nucleosome into the "on" position by the DNA-dependent ATPase CSB (Cockayne syndrome protein B). The results uncover a unique mechanism by which ATP-dependent chromatin remodeling complexes with opposing activities establish a specific chromatin state and regulate transcription.
URI http://hdl.handle.net/20.500.11897/343416
ISSN 0027-8424
DOI 10.1073/pnas.1201262109
Indexed SCI(E)
PubMed
Appears in Collections: 细胞增殖分化调控机理研究教育部重点实验室

Files in This Work
There are no files associated with this item.

Web of Science®


94

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.