タナベ ケンジ
Tanabe Kenji
田邊 賢司 所属 研究施設 研究施設 職種 准教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Dynamin 2 associates with microtubules at mitosis and regulates cell cycle progression. |
掲載誌名 | 正式名:Cell Structure and Function |
巻・号・頁 | 36,pp.145-154 |
著者・共著者 | Ishida, Nobuhisa Nakamura, Yuichi Tanabe, Kenj i Li, Shun-Ai Takei, Kohji |
担当区分 | 筆頭著者,責任著者 |
発行年月 | 2011 |
概要 | Dynamin, a ~100 kDa large GTPase, is known as a key player for membrane traffic. Recent evidence shows that dynamin also regulates the dynamic instability of microtubules by a mechanism independent of membrane traffic. As microtubules are highly dynamic during mitosis, we investigated whether the regulation of microtubules by dynamin is essential for cell cycle progression. Dynamin 2 intensely localized at the mitotic spindle, and the localization depended on its proline-rich domain (PRD), which is required for microtubule association. The deletion of PRD resulted in the impairment of cytokinesis, whereby the mutant had less effect on endocytosis. Interestingly, dominant-negative dynamin (K44A), which blocks membrane traffic but has no effect on microtubules, also blocked cytokinesis. On the other hand, the deletion of the middle domain, which binds to γ-tubulin, impaired the entry into mitosis. As both deletion mutants had no significant effect on endocytosis, dynamin 2 may participate in cell cycle progression by regulating the microtubules. These data suggest that dynamin may play a key role for cell cycle progression by twodistinct pathways, membrane traffic and cytoskeleton. |