Papers

Peer-reviewed
Dec, 2013

Murine esBAF chromatin remodeling complex subunits BAF250a and Brg1 are necessary to maintain and reprogram pluripotency-specific replication timing of select replication domains

EPIGENETICS & CHROMATIN
  • Shin-ichiro Takebayashi
  • Ienglam Lei
  • Tyrone Ryba
  • Takayo Sasaki
  • Vishnu Dileep
  • Dana Battaglia
  • Xiaolin Gao
  • Peng Fang
  • Yong Fan
  • Miguel A. Esteban
  • Jiong Tang
  • Gerald R. Crabtree
  • Zhong Wang
  • David M. Gilbert
  • Display all

Volume
6
Number
First page
42
Last page
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1186/1756-8935-6-42
Publisher
BIOMED CENTRAL LTD

Background: Cellular differentiation and reprogramming are accompanied by changes in replication timing and 3D organization of large-scale (400 to 800 Kb) chromosomal domains ('replication domains'), but few gene products have been identified whose disruption affects these properties.
Results: Here we show that deletion of esBAF chromatin-remodeling complex components BAF250a and Brg1, but not BAF53a, disrupts replication timing at specific replication domains. Also, BAF250a-deficient fibroblasts reprogrammed to a pluripotency-like state failed to reprogram replication timing in many of these same domains. About half of the replication domains affected by Brg1 loss were also affected by BAF250a loss, but a much larger set of domains was affected by BAF250a loss. esBAF binding in the affected replication domains was dependent upon BAF250a but, most affected domains did not contain genes whose transcription was affected by loss of esBAF.
Conclusions: Loss of specific esBAF complex subunits alters replication timing of select replication domains in pluripotent cells.

Link information
DOI
https://doi.org/10.1186/1756-8935-6-42
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000330071200001&DestApp=WOS_CPL
ID information
  • DOI : 10.1186/1756-8935-6-42
  • ISSN : 1756-8935
  • Web of Science ID : WOS:000330071200001

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