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Rab11 和 Arf6 在调节有丝分裂细胞中 Rab11-FIP3/arfophilin-1 定位中的不同作用。

Distinct roles of Rab11 and Arf6 in the regulation of Rab11-FIP3/arfophilin-1 localization in mitotic cells.

机构信息

Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Japan.

出版信息

Genes Cells. 2011 Sep;16(9):938-50. doi: 10.1111/j.1365-2443.2011.01538.x. Epub 2011 Jul 25.

Abstract

Rab11 family interacting protein 3/arfophilin-1 is a dual effector of Rab11 and Arf6 and exhibits Rab11-dependent localization to recycling endosomes in interphase. Furthermore, FIP3 undergoes dynamic redistribution to the intercellular bridge during cytokinesis. However, regulation of FIP3 redistribution and its local function by Rab11 and Arf6 has remained controversial. In this study, we developed a procedure for detecting endogenous FIP3, Arf6, and Rab11 and determined that FIP3 is localized near the intercellular bridge during cytokinesis, and to the Flemming body (the midbody) immediately before abscission; Rab11 is localized near the intercellular bridge, but not to the Flemming body; and Arf6 is localized to the Flemming body. Time-lapse analyses showed that FIP3 is transported to the intercellular bridge during cytokinesis, together with Rab11; before abscission, FIP3 becomes localized to the Flemming body, where Arf6 is already present. After abscission, FIP3 and Arf6 are incorporated into one of the daughter cells as a Flemming body remnant. Based on these observations, we propose that FIP3 localization to recycling endosomes in interphase and their transport to the intercellular bridge during cytokinesis depend on Rab11, and targeting of FIP3-positive endosomal vesicles to the Flemming body in the abscission phase depends on Arf6.

摘要

Rab11 家族相互作用蛋白 3/arfophilin-1 是 Rab11 和 Arf6 的双重效应物,在细胞间期中表现出 Rab11 依赖性定位到再循环内体。此外,FIP3 在有丝分裂期间经历动态再分布到细胞间桥。然而,Rab11 和 Arf6 对 FIP3 再分布及其局部功能的调节仍存在争议。在这项研究中,我们开发了一种检测内源性 FIP3、Arf6 和 Rab11 的程序,并确定 FIP3 在有丝分裂期间定位于细胞间桥附近,并在分离前立即定位于 Fleming 体(中体);Rab11 定位于细胞间桥附近,但不定位于 Fleming 体;Arf6 定位于 Fleming 体。延时分析表明,FIP3 在有丝分裂期间与 Rab11 一起被运送到细胞间桥;在分离前,FIP3 被定位到 Fleming 体,那里已经存在 Arf6。分离后,FIP3 和 Arf6 作为 Fleming 体残余物之一被纳入一个子细胞中。基于这些观察结果,我们提出 FIP3 在细胞间期中定位于再循环内体及其在有丝分裂期间向细胞间桥的运输依赖于 Rab11,而 FIP3 阳性内体囊泡向分离期 Fleming 体的靶向依赖于 Arf6。

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