spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online March 21, 2008


Development 135, 805e (2008)
© The Company of Biologists Limited
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Development
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

In this issue

Running Rings around ES cell pluripotency


Figure 1

The maintenance of embryonic stem (ES) cell pluripotency depends on a core transcriptional regulatory network that represses key transcription factors involved in differentiation and development. The Polycomb group (PcG) of proteins mediate the heritable silencing of developmental regulators, but are the PcG proteins and this transcriptional network functionally linked? Endoh and co-workers now show that the Polycomb repressive complex 1 (PRC1) components Ring1A/B act downstream of the core transcriptional regulatory circuitry that maintains mouse ES cell self renewal (see p. 1513). Ring1A/B, they show, are essential for maintaining undifferentiated ES cells through their repression of certain developmental regulators that direct ES cell differentiation. This silencing, which is achieved through the inhibition of chromatin remodelling, depends on a key component of the core transcription network: Oct3/4. But Oct3/4 also binds to these targets independently of PRC1. These and other results clearly show that a functional link between Ring1A/B-mediated PRC1 silencing and the core transcriptional regulatory circuitry acts to maintain ES cell self renewal.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?

Related articles in Development:

Polycomb group proteins Ring1A/B are functionally linked to the core transcriptional regulatory circuitry to maintain ES cell identity
Mitsuhiro Endoh, Takaho A. Endo, Tamie Endoh, Yu-ichi Fujimura, Osamu Ohara, Tetsuro Toyoda, Arie P. Otte, Masaki Okano, Neil Brockdorff, Miguel Vidal, and Haruhiko Koseki
Development 2008 135: 1513-1524. [Abstract] [Full Text]  




This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Development
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?