Spermatocyte cytokinesis requires rapid membrane addition mediated by ARF6 on central spindle recycling endosomes

被引:82
作者
Dyer, Naomi
Rebollo, Elena
Dominguez, Paloma
Elkhatib, Nadia
Chavrier, Philippe
Daviet, Laurent
Gonzalez, Cayetano
Gonzalez-Gaitan, Marcos [1 ]
机构
[1] Max Planck Inst Mol Cell Biol Genet, D-01307 Dresden, Germany
[2] Univ Liverpool, Liverpool Sch Trop Med, Liverpool L3 5QA, Merseyside, England
[3] Inst Catalana Rec & Estudy Avancats, E-08028 Barcelona, Spain
[4] Inst Curie, CNRS, UMR 144, Membrane & Cytoskleton Dynam Grp, F-75005 Paris, France
[5] Hybrigen SA, F-75014 Paris, France
[6] Univ Geneva, Dept Biochem, CH-1211 Geneva, Switzerland
来源
DEVELOPMENT | 2007年 / 134卷 / 24期
关键词
Drosophila; meiosis; spermatogenesis; testis;
D O I
10.1242/dev.010983
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The dramatic cell shape changes during cytokinesis require the interplay between microtubules and the actomyosin contractile ring, and addition of membrane to the plasma membrane. Numerous membrane-trafficking components localize to the central spindle during cytokinesis, but it is still unclear how this machinery is targeted there and how membrane trafficking is coordinated with cleavage furrow ingression. Here we use an arf6 null mutant to show that the endosomal GTPase ARF6 is required for cytokinesis in Drosophila spermatocytes. ARF6 is enriched on recycling endosomes at the central spindle, but it is required neither for central spindle nor actomyosin contractile ring assembly, nor for targeting of recycling endosomes to the central spindle. However, in arf6 mutants the cleavage furrow regresses because of a failure in rapid membrane addition to the plasma membrane. We propose that ARF6 promotes rapid recycling of endosomal membrane stores during cytokinesis, which is critical for rapid cleavage furrow ingression.
引用
收藏
页码:4437 / 4447
页数:11
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