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


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search    

The fully linked HTML version of this article has now been published.
Development ePress online publication date 13 Aug 2008
doi: 10.1242/dev.021923


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.021923v1
135/18/3021    most recent
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 Similar articles in this journal
Right arrow Similar articles in PubMed
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chang, P.-J.
Right arrow Articles by Pi, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chang, P.-J.
Right arrow Articles by Pi, H.
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?

Research article

Negative-feedback regulation of proneural proteins controls the timing of neural precursor division


Pao-Ju Chang, Yun-Ling Hsiao, An-Chi Tien, Yi-Chen Li, and Haiwei Pi*
* Author for correspondence (e-mail: haiwei{at}mail.cgu.edu.tw)

Neurogenesis requires precise control of cell specification and division. In Drosophila, the timing of cell division of the sensory organ precursor (SOP) is under strict temporal control. But how the timing of mitotic entry is determined remains poorly understood. Here, we present evidence that the timing of the G2-M transition is determined by when proneural proteins are degraded from SOPs. This process requires the E3 ubiquitin ligase complex, including the RING protein Sina and the adaptor Phyl. In phyl mutants, proneural proteins accumulate, causing delay or arrest in the G2-M transition. The G2-M defect in phyl mutants is rescued by reducing the ac and sc gene doses. Misexpression of phyl downregulates proneural protein levels in a sina-dependent manner. Phyl directly associates with proneural proteins to act as a bridge between proneural proteins and Sina. As phyl is a direct transcriptional target of Ac and Sc, our data suggest that, in addition to mediating cell cycle arrest, proneural protein initiates a negative-feedback regulation to time the mitotic entry of neural precursors.


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?


This article has been cited by other articles:


Home page
GeneticsHome page
A. Garcia-Bellido and J. F. de Celis
The Complex Tale of the achaete-scute Complex: A Paradigmatic Case in the Analysis of Gene Organization and Function During Development
Genetics, July 1, 2009; 182(3): 631 - 639.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
P.-J. Chang, Y.-L. Hsiao, A.-C. Tien, Y.-C. Li, and H. Pi
Negative-feedback regulation of proneural proteins controls the timing of neural precursor division
J. Cell Sci., September 15, 2008; 121(18): e1806 - e1806.
[Full Text]




© The Company of Biologists Ltd 2008