A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Reference Report

Reference
Citation Fuse, N., Hisata, K., Katzen, A.L., Matsuzaki, F. (2003). Heterotrimeric g proteins regulate daughter cell size asymmetry in Drosophila neuroblast divisions.  Curr. Biol. 13(11): 947--954. (Export to RIS)
FlyBase ID FBrf0159715
Publication Type Research paper
External Crossreferences
PubMed ID 12781133
PubMed Abstract Cell division often generates unequally sized daughter cells by off-center cleavages, which are due to either displacement of mitotic spindles or their asymmetry. Drosophila neuroblasts predominantly use the latter mechanism to divide into a large apical neuroblast and a small basal ganglion mother cell (GMC), where the neural fate determinants segregate. Apically localized components regulate both the spindle asymmetry and the localization of the determinants. Here, we show that asymmetric spindle formation depends on signaling mediated by the G beta subunit of heterotrimeric G proteins. G beta 13F distributes throughout the neuroblast cortex. Its lack induces a large symmetric spindle and causes division into nearly equal-sized cells with normal segregation of the determinants. In contrast, elevated G beta 13F activity generates a small spindle, suggesting that this factor suppresses spindle development. Depletion of the apical components also results in the formation of a small symmetric spindle at metaphase. Therefore, the apical components and G beta 13F affect the mitotic spindle shape oppositely. We propose that differential activation of G beta signaling biases spindle development within neuroblasts and thereby causes asymmetric spindles. Furthermore, the multiple equal cleavages of G beta mutant neuroblasts accompany neural defects; this finding suggests indispensable roles of eccentric division in assuring the stem cell properties of neuroblasts.
BIOSIS ID 2003.384254
Zoological Record ID
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2012_01
FB2011_10
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Associated Information
Comments
Text of Personal Communication
Associated Files
hide Other Information
Secondary IDs
Language of Publication English
Additional Languages of Abstract
ISBN
hide Parent Publication
Publication Type Journal
Abbreviation Curr. Biol.
Title Current Biology
Editors
Publication Year 1991-
ISBN/ISSN 0960-9822
hide Data from Reference
hideAlleles (16)
hideConstructs (9)
hideGenes (27)
hideInsertions (1)