Actin and Endocytosis in Budding Yeast

被引:163
|
作者
Goode, Bruce L. [1 ]
Eskin, Julian A. [1 ]
Wendland, Beverly [2 ]
机构
[1] Brandeis Univ, Dept Biol, Rosenstiel Ctr, Waltham, MA 02454 USA
[2] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
S; cerevisiae; Arp2/3; complex; clathrin; membrane; endocytosis; CLATHRIN-MEDIATED ENDOCYTOSIS; CYCLASE-ASSOCIATED PROTEIN; ACANTHAMOEBA ACTOPHORIN ADF/COFILIN; FILAMENT BRANCH FORMATION; ALDRICH-SYNDROME PROTEIN; MONOMER-BINDING-PROTEIN; FACTOR HOMOLOGY DOMAIN; ELONGATION-FACTOR; 1A; HUMAN ARP2/3 COMPLEX; SACCHAROMYCES-CEREVISIAE;
D O I
10.1534/genetics.112.145540
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Endocytosis, the process whereby the plasma membrane invaginates to form vesicles, is essential for bringing many substances into the cell and for membrane turnover. The mechanism driving clathrin-mediated endocytosis (CME) involves > 50 different protein components assembling at a single location on the plasma membrane in a temporally ordered and hierarchal pathway. These proteins perform precisely choreographed steps that promote receptor recognition and clustering, membrane remodeling, and force-generating actin-filament assembly and turnover to drive membrane invagination and vesicle scission. Many critical aspects of the CME mechanism are conserved from yeast to mammals and were first elucidated in yeast, demonstrating that it is a powerful system for studying endocytosis. In this review, we describe our current mechanistic understanding of each step in the process of yeast CME, and the essential roles played by actin polymerization at these sites, while providing a historical perspective of how the landscape has changed since the preceding version of the YeastBook was published 17 years ago (1997). Finally, we discuss the key unresolved issues and where future studies might be headed.
引用
收藏
页码:315 / 358
页数:44
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