Haas Alexander K, Yoshimura Shin-ichiro, Stephens David J, Preisinger Christian, Fuchs Evelyn, Barr Francis A
Cancer Research Centre, University of Liverpool, 200 London Road, Liverpool, L9 3AT, UK.
J Cell Sci. 2007 Sep 1;120(Pt 17):2997-3010. doi: 10.1242/jcs.014225. Epub 2007 Aug 7.
Rab GTPases control vesicle movement and tethering membrane events in membrane trafficking. We used the 38 human Rab GTPase activating proteins (GAPs) to identify which of the 60 Rabs encoded in the human genome function at the Golgi complex. Surprisingly, this screen identified only two GAPs, RN-tre and TBC1D20, disrupting both Golgi organization and protein transport. RN-tre is the GAP for Rab43, and controls retrograde transport into the Golgi from the endocytic pathway. TBC1D20 is the ER-localized GAP for Rab1, and is the only GAP blocking the delivery of secretory cargo from the ER to the cell surface. Strikingly, its expression causes the loss of the Golgi complex, highlighting the importance of Rab1 for Golgi biogenesis. These effects can be antagonized by reticulon, a binding partner for TBC1D20 in the ER. Together, these findings indicate that Rab1 and Rab43 are key Rabs required for the biogenesis and maintenance of a functional Golgi structure, and suggest that other Rabs acting at the Golgi complex are likely to be functionally redundant.
Rab GTP酶在膜运输过程中控制囊泡移动和膜系留事件。我们利用38种人类Rab GTP酶激活蛋白(GAP)来确定人类基因组中编码的60种Rab蛋白中哪些在高尔基体复合体发挥作用。令人惊讶的是,该筛选仅鉴定出两种GAP,即RN-tre和TBC1D20,它们会破坏高尔基体的组织和蛋白质运输。RN-tre是Rab43的GAP,控制从内吞途径逆向运输至高尔基体。TBC1D20是内质网定位的Rab1的GAP,是唯一阻断分泌性货物从内质网运输至细胞表面的GAP。引人注目的是,其表达会导致高尔基体复合体的丧失,突出了Rab1对高尔基体生物发生的重要性。这些效应可被网织蛋白拮抗,网织蛋白是TBC1D20在内质网中的结合伴侣。总之,这些发现表明Rab1和Rab43是功能性高尔基体结构生物发生和维持所需的关键Rab蛋白,并表明在高尔基体复合体发挥作用的其他Rab蛋白可能在功能上是冗余的。