A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Lee, S., Zhou, L., Kim, J., Kalbfleisch, S., Schöck, F. (2008). Lasp anchors the Drosophila male stem cell niche and mediates spermatid individualization.  Mech. Dev. 125(9-10): 768--776. (Export to RIS)
FlyBase ID FBrf0207050
Publication Type Research paper
PubMed ID 18655828
PubMed Abstract Lasp family proteins contain an amino-terminal LIM domain, two actin-binding nebulin repeats and a carboxyl-terminal SH3 domain. Vertebrate Lasp-1 localizes to focal adhesions and the leading edge of migrating cells, and is required for cell migration. To assess the in vivo function of Lasp, we generated a null mutant in Drosophila Lasp. Lasp(1) is homozygous viable, but male sterile. In Lasp mutants the stem cell niche is no longer anchored to the apical tip of the testis, and actin cone migration is perturbed resulting in improper spermatid individualization. Hub cell mislocalization can by phenocopied by expressing Lasp or betaPS integrin RNAi transgenes in somatic cells, and Lasp genetically interacts with betaPS integrin, demonstrating that Lasp functions together with integrins in hub cells to anchor the stem cell niche. Finally, we show that the stem cell niche is maintained even if it is not properly localized.
DOI 10.1016/j.mod.2008.06.012
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Language of Publication English
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Publication Type Journal
Abbreviation Mech. Dev.
Title Mechanisms of Development
Publication Year 1990-
ISBN/ISSN 0925-4773
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