JCB logo
amgmicro.com
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 23 January 2006. doi:10.1083/jcb1723rr4
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 172, Number 3, 326-326
This Article
Right arrow Full Text (PDF, 837K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Katsnelson, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Katsnelson, A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Research Roundup

Hyperdynamic proteins keep stem cells on their toes



Figure 1
Chromatin protein dynamics (measured by fluorescence recovery) is fast in ES cells (white) but slower in differentiating (red) or differentiated (black) cells.

MISTELI/ELSEVIER

Chromatin has a staid and static image. But Eran Meshorer, Tom Misteli (National Cancer Institute, Bethesda, MD), and colleagues suggest that ES cells are kept pluripotent thanks to hyperactively mobile chromatin proteins.

Chromatin proteins provide architectural integrity to DNA. Despite their structural role, they do not stay statically bound but release and reform their bonds continuously. Using FRAP to measure protein dynamics, the group showed that chromatin proteins in differentiated cells are exchanged within minutes to hours, whereas ES cells contain a pool of such proteins that turns over at the rate of seconds. The fast-moving protein fraction is present in several types of pluripotent cells but strikingly absent in committed precursor cells. This quick exchange may be what keeps the genome breathing—open and ready to take on any fate.

Frenetic protein activity also seems to be necessary for differentiation. When chromatin proteins were mutated to bind more tightly to DNA, cells failed to differentiate, whereas mutations increasing the pool of loose proteins led to faster than normal differentiation. The team postulates that in ES cells the proteins may be acting as building blocks where regions of silent (nontranscribing) chromatin are formed as the cell differentiates and shuts down unused areas of the genome.

Misteli hints that chromatin protein dynamics is probably just the tip of the iceberg in the search for what distinguishes pluripotent cells from committed ones, and says the group is looking for other properties of chromatin, such as histone modifications, gene activity, and chromatin structure that may differ in ES cells. They are also examining the underlying question of what the mobility might mean for gene expression. "If [ES] chromatin is really more open," he says, "there might be more transcription."Formula

Reference:

Meshorer, E., et al. 2006. Dev. Cell. 10:105–116.[CrossRef][Medline]



Alla Katsnelson

akatsnelson{at}fastmail.fm


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 Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?



This Article
Right arrow Full Text (PDF, 837K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Katsnelson, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Katsnelson, A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents