The Msx1 Homeoprotein Recruits Polycomb to the Nuclear Periphery during Development
Author(s)
Wang, Jingqiang; Kumar, Roshan M.; Biggs, Vanessa J.; Lee, Hansol; Chen, Yun; Kagey, Michael H.; Young, Richard A.; Abate-Shen, Cory; ... Show more Show less
DownloadWang-2011-The Msx1 Homeoprotei.pdf (2.365Mb)
PUBLISHER_POLICY
Publisher Policy
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Terms of use
Metadata
Show full item recordAbstract
Control of gene expression during development requires the concerted action of sequence-specific transcriptional regulators and epigenetic modifiers, which are spatially coordinated within the nucleus through mechanisms that are poorly understood. Here we show that transcriptional repression by the Msx1 homeoprotein in myoblast cells requires the recruitment of Polycomb to target genes located at the nuclear periphery. Target genes repressed by Msx1 display an Msx1-dependent enrichment of Polycomb-directed trimethylation of lysine 27 on histone H3 (H3K27me3). Association of Msx1 with the Polycomb complex is required for repression and regulation of myoblast differentiation. Furthermore, Msx1 promotes a dynamic spatial redistribution of the H3K27me3 repressive mark to the nuclear periphery in myoblast cells and the developing limb in vivo. Our findings illustrate a hitherto unappreciated spatial coordination of transcription factors with the Polycomb complex for appropriate regulation of gene expression programs during development.
Date issued
2011-08Department
Massachusetts Institute of Technology. Department of Biology; Whitehead Institute for Biomedical ResearchJournal
Developmental Cell
Publisher
Elsevier
Citation
Wang, Jingqiang, Roshan M. Kumar, Vanessa J. Biggs, Hansol Lee, Yun Chen, Michael H. Kagey, Richard A. Young, and Cory Abate-Shen. “The Msx1 Homeoprotein Recruits Polycomb to the Nuclear Periphery During Development.” Developmental Cell 21, no. 3 (September 2011): 575–588. © 2011 Elsevier Inc.
Version: Final published version
ISSN
15345807
1878-1551