A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Steinhauer, J., Gijón, M.A., Riekhof, W.R., Voelker, D.R., Murphy, R.C., Treisman, J.E. (2009). Drosophila Lysophospholipid Acyltransferases Are Specifically Required for Germ Cell Development.  Mol. Biol. Cell 20(24): 5224--5235. (Export to RIS)
FlyBase ID FBrf0209500
Publication Type Research paper
PubMed ID 19864461
PubMed Abstract Enzymes of the membrane-bound O-acyltransferase (MBOAT) family add fatty acyl chains to a diverse range of protein and lipid substrates. A chromosomal translocation disrupting human MBOAT1 results in a novel syndrome characterized by male sterility and brachydactyly. We have found that the Drosophila homologues of MBOAT1, Oysgedart (Oys), Nessy (Nes), and Farjavit (Frj), are lysophospholipid acyltransferases. When expressed in yeast, these MBOATs esterify specific lysophospholipids preferentially with unsaturated fatty acids. Generating null mutations for each gene allowed us to identify redundant functions for Oys and Nes in two distinct aspects of Drosophila germ cell development. Embryos lacking both oys and nes show defects in the ability of germ cells to migrate into the mesoderm, a process guided by lipid signals. In addition, oys nes double mutant adult males are sterile due to specific defects in spermatid individualization. oys nes mutant testes, as well as single, double, and triple mutant whole adult animals, show an increase in the saturated fatty acid content of several phospholipid species. Our findings suggest that lysophospholipid acyltransferase activity is essential for germline development and could provide a mechanistic explanation for the etiology of the human MBOAT1 mutation.
DOI 10.1091/mbc.E09-05-0382
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Language of Publication English
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Publication Type Journal
Abbreviation Mol. Biol. Cell
Title Molecular Biology of the Cell
Publication Year 1992-
ISBN/ISSN 1059-1524
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