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BIG2和BIG1的冗余作用,这两种ADP核糖基化因子的鸟嘌呤核苷酸交换因子在反式高尔基体网络和内体之间的膜运输中发挥作用。

Redundant roles of BIG2 and BIG1, guanine-nucleotide exchange factors for ADP-ribosylation factors in membrane traffic between the trans-Golgi network and endosomes.

作者信息

Ishizaki Ray, Shin Hye-Won, Mitsuhashi Hiroko, Nakayama Kazuhisa

机构信息

Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan.

出版信息

Mol Biol Cell. 2008 Jun;19(6):2650-60. doi: 10.1091/mbc.e07-10-1067. Epub 2008 Apr 16.

Abstract

BIG2 and BIG1 are closely related guanine-nucleotide exchange factors (GEFs) for ADP-ribosylation factors (ARFs) and are involved in the regulation of membrane traffic through activating ARFs and recruiting coat protein complexes, such as the COPI complex and the AP-1 clathrin adaptor complex. Although both ARF-GEFs are associated mainly with the trans-Golgi network (TGN) and BIG2 is also associated with recycling endosomes, it is unclear whether BIG2 and BIG1 share some roles in membrane traffic. We here show that knockdown of both BIG2 and BIG1 by RNAi causes mislocalization of a subset of proteins associated with the TGN and recycling endosomes and blocks retrograde transport of furin from late endosomes to the TGN. Similar mislocalization and protein transport block, including furin, were observed in cells depleted of AP-1. Taken together with previous reports, these observations indicate that BIG2 and BIG1 play redundant roles in trafficking between the TGN and endosomes that involves the AP-1 complex.

摘要

BIG2和BIG1是与ADP核糖基化因子(ARF)密切相关的鸟嘌呤核苷酸交换因子(GEF),通过激活ARF和募集诸如COPI复合体和AP-1网格蛋白衔接复合体等衣被蛋白复合体参与膜运输的调控。尽管这两种ARF-GEF主要都与反式高尔基体网络(TGN)相关,且BIG2还与再循环内体相关,但尚不清楚BIG2和BIG1在膜运输中是否具有某些共同作用。我们在此表明,通过RNA干扰敲低BIG2和BIG1会导致与TGN和再循环内体相关的一部分蛋白质定位错误,并阻断弗林蛋白酶从晚期内体到TGN的逆行运输。在AP-1缺失的细胞中也观察到了类似的定位错误和蛋白质运输阻断,包括弗林蛋白酶。结合先前的报道,这些观察结果表明,BIG2和BIG1在涉及AP-1复合体的TGN和内体之间的运输中发挥冗余作用。

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