Hanai Ayako, Ohgi Minako, Yagi Chikako, Ueda Tomoko, Shin Hye-Won, Nakayama Kazuhisa
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan
J Biochem. 2016 Feb;159(2):201-8. doi: 10.1093/jb/mvv088. Epub 2015 Sep 1.
Small GTPases play important roles in various aspects of cell division as well as membrane trafficking. We and others previously showed that ADP-ribosylation factor 6 (Arf6) is locally activated around the ingressing cleavage furrow and recruited to the Flemming body in late cytokinesis phases, and involved in faithful completion of cytokinesis. However, knockout of the Arf6 gene or Arf6 depletion by siRNAs did not drastically influence cytokinesis. We here show that, in addition to Arf6, Class I Arfs (Arf1 and Arf3) are localized to the Flemming body, and that double knockdown of Arf1 and Arf3 moderately increases the proportion of multinucleate cells and simultaneous knockdown of Arf1, Arf3 and Arf6 leads to severe cytokinesis defects. These observations indicate that Arf1 and Arf3 as well as Arf6 play important roles in cytokinesis. We further show that EFA6 (exchange factor for Arf6) activates not only Arf6 but also Arf1 in the cell. Taken together with our previous data, these Arf GTPases are likely to be locally activated by EFA6 and in turn targeted to the Flemming body to complete cytokinesis.
小GTP酶在细胞分裂以及膜运输的各个方面都发挥着重要作用。我们和其他研究人员之前表明,ADP核糖基化因子6(Arf6)在进入的分裂沟周围局部激活,并在胞质分裂后期被招募到弗莱明体,参与胞质分裂的顺利完成。然而,Arf6基因敲除或通过小干扰RNA(siRNA)耗尽Arf6并没有对胞质分裂产生显著影响。我们在此表明,除了Arf6之外,I类Arf(Arf1和Arf3)也定位于弗莱明体,并且Arf1和Arf3的双重敲低适度增加了多核细胞的比例,而Arf1、Arf3和Arf6的同时敲低会导致严重的胞质分裂缺陷。这些观察结果表明,Arf1、Arf3以及Arf6在胞质分裂中发挥着重要作用。我们进一步表明,EFA6(Arf6的交换因子)在细胞中不仅激活Arf6,还激活Arf1。结合我们之前的数据,这些Arf GTP酶可能被EFA6局部激活,进而靶向弗莱明体以完成胞质分裂。