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

Published 18 February 2002. doi:10.1083/jcb1564rr1
This Article
Right arrow Full Text (PDF, 169K)
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.
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?

© The Rockefeller University Press, 0021-9525/2002/2/588 $5.00
The Journal of Cell Biology, Volume 156, Number 4, February 18, 2002 588-588


Research Roundup

Sex, Sox, and splicing


SRY (red) colocalizes with a splicing factor (green) in nuclear speckles.

Sassone-Corsi/NAS

Mammalian sex-determining factors with homology to DNA binding proteins are required for splicing, according to a study by Paolo Sassone-Corsi and coworkers at the Université Louis Pasteur (Strasbourg, France). Examination of high mobility group (HMG) domain containing SRY and Sox proteins demonstrated a surprising but clear association with splicing complexes.

SRY, the testis-determining factor found on the Y-chromosome in mice and humans, is one of several Sox family members involved in sexual development. It is known to bind DNA, in support of the proposal that HMG domain proteins act as architectural facilitators for building transcription complexes.

Sassone-Corsi's group thus expected to find Sox proteins colocalized in the nucleus with transcription factors. Instead, SRY and SOX6 proteins associated with splicing factors in nuclear speckle domains. Depletion of SOX6 in HeLa cell extracts blocked splicing of multiple substrates, and expression of the HMG domain only of either SOX6, SOX9, or SRY restored splicing in the extracts, indicating functional overlap of the proteins.

The group's results provide the first association between splicing and sex determination in mammals. The Drosophila genes transformer and sex-lethal encode mRNA splicing factors required for sex determination in flies, indicating that regulated splicing of sex-determining factors may be evolutionarily conserved. According to Sassone-Corsi, to complete the connection "the next step is to identify natural physiological substrates of the Sox and SRY proteins." He thinks the Sox proteins may control regulated splicing by determining which spliceosomal complexes are formed in different cell types, analogous to the way transcription factors can regulate the basal transcription machinery. {blacksquare}

Reference:

Ohe, K., et al. 2002. Proc. Natl. Acad. Sci. USA. 99:1146–1151.[Abstract/Free Full Text]

SRY (red) colocalizes with a splicing factor (green) in nuclear speckles.

Sassone-Corsi/NAS



Nicole LeBrasseur

labrasn{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?



This Article
Right arrow Full Text (PDF, 169K)
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.
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