JCB logo
Avanti Polar Lipids, Inc.
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published 13 September 2004. doi:10.1083/jcb1666iti3
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 166, Number 6, 761-761
This Article
Right arrow Full Text (PDF, 903K)
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 LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Related Collections
Right arrowRelated Article
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?

In This Issue

Hitched genes still independent



A gene's association with perinuclear heterochromatin (bars) is not restricted by its neighbor's location.

Transcribed genes move away from heterochromatin even if their silent neighbors do not, as shown by Zink et al. (page 815).

Transcriptional status is closely related to nuclear positioning. Silenced genes, for example, are often associated with heterochromatin at the nuclear periphery, whereas active genes occupy different nuclear domains. The new results show that even close linkage to genes that are not transcribed does not prevent an activated gene from leaving heterochromatin.

The authors imaged three adjacent genes, CFTR (mutations in which cause cystic fibrosis), and its closest neighbors, GASZ and CORTBP2, in various cell types. When none of the genes were expressed, all three were closely associated with the nuclear envelope and peripheral heterochromatin. In cells that transcribed only one or two of the genes, only the active ones were found in the nuclear interior, separated from heterochromatin.

Repositioning might be controlled by histone modifications, which can be stably inherited through mitosis. Chemically induced histone acetylation pushed CFTR from the periphery into the interior. CFTR transcription was not activated, at least in the short term, but positioning may be important for maintaining transcriptional status. If so, gene therapy strategies for cystic fibrosis may need to overcome this additional layer of complexity. {blacksquare}



Nicole LeBrasseur

lebrasn{at}rockefeller.edu


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?

Related Article

Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei
Daniele Zink, Margarida D. Amaral, Andreas Englmann, Susanne Lang, Luka A. Clarke, Carsten Rudolph, Felix Alt, Kathrin Luther, Carla Braz, Nicolas Sadoni, Joseph Rosenecker, and Dirk Schindelhauer
J. Cell Biol. 2004 166: 815-825. [Abstract] [Full Text] [PDF]




This Article
Right arrow Full Text (PDF, 903K)
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 LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Related Collections
Right arrowRelated Article
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