Dyer Naomi, Rebollo Elena, Domínguez Paloma, Elkhatib Nadia, Chavrier Philippe, Daviet Laurent, González Cayetano, González-Gaitán Marcos
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.
Development. 2007 Dec;134(24):4437-47. doi: 10.1242/dev.010983.
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.
胞质分裂过程中细胞形状的剧烈变化需要微管与肌动球蛋白收缩环之间的相互作用,以及向质膜添加膜成分。许多膜运输成分在胞质分裂期间定位于中央纺锤体,但目前仍不清楚该机制是如何靶向到那里的,以及膜运输是如何与分裂沟的内陷协调的。在这里,我们使用arf6基因敲除突变体来表明内体GTP酶ARF6是果蝇精母细胞胞质分裂所必需的。ARF6在中央纺锤体的回收内体上富集,但它对于中央纺锤体或肌动球蛋白收缩环的组装不是必需的,也不是回收内体靶向中央纺锤体所必需的。然而,在arf6突变体中,由于无法快速向质膜添加膜,分裂沟会退缩。我们提出,ARF6在胞质分裂过程中促进内体膜储存的快速循环,这对于分裂沟的快速内陷至关重要。