Analysis of protein dynamics during cytokinesis in budding yeast

被引:8
|
作者
Okada, S. [1 ,2 ]
Wloka, C. [1 ,3 ]
Bi, E. [1 ]
机构
[1] Univ Penn, Philadelphia, PA 19104 USA
[2] Kyushu Univ, Fukuoka, Japan
[3] Univ Groningen, Groningen, Netherlands
来源
CYTOKINESIS | 2017年 / 137卷
关键词
MYOSIN-II; SACCHAROMYCES-CEREVISIAE; FISSION YEAST; CONTRACTILE RING; SEPTUM FORMATION; ACTIN-RING; MITOTIC EXIT; CELL-CYCLE; POLARITY; ACTOMYOSIN;
D O I
10.1016/bs.mcb.2016.04.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytokinesis is essential for development and survival of all organisms by increasing cell number and diversity. It is a highly regulated process that requires spatiotemporal coordination of hundreds of proteins functioning in the assembly, constriction, and disassembly of a contractile actomyosin ring, targeted vesicle fusion, and localized extracellular matrix remodeling. Cytokinesis has been studied in multiple systems with a wide range of technologies to learn the common principles. In this chapter, we describe the analysis of protein dynamics during cytokinesis in the budding yeast Saccharomyces cerevisiae by several live-cell imaging methods. This, in combination with the power of yeast genetics, has yielded novel insights into the mechanism of cytokinesis. Similar approaches are increasingly used to study this fundamental process in more complex systems.
引用
收藏
页码:25 / 45
页数:21
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