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Mitotic phosphorylation of Exo84 disrupts exocyst assembly and arrests cell growth
被引:30
作者:
Luo, Guangzuo
[1
]
Zhang, Jian
[1
]
Luca, Francis C.
[2
]
Guo, Wei
[1
]
机构:
[1] Univ Penn, Dept Biol, Sch Arts & Sci, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Anim Biol, Sch Vet Med, Philadelphia, PA 19104 USA
关键词:
DEPENDENT KINASE CDK1;
SACCHAROMYCES-CEREVISIAE;
PLASMA-MEMBRANE;
PROTEIN-KINASE;
SECRETORY PATHWAY;
GOLGI-APPARATUS;
BUDDING YEAST;
ANIMAL-CELLS;
MITOSIS;
CYCLE;
D O I:
10.1083/jcb.201211093
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The rate of eukaryotic cell growth is tightly controlled for proper progression through each cell cycle stage and is important for cell size homeostasis. It was previously shown that cell growth is inhibited during mitosis when cells are preparing for division. However, the mechanism for growth arrest at this stage is unknown. Here we demonstrate that exocytosis of a select group of cargoes was inhibited before the metaphase-anaphase transition in the budding yeast Saccharomyces cerevisiae. The cyclin-dependent kinase, Cdk1, when bound to the mitotic cyclin Clb2, directly phosphorylated Exo84, a component of the exocyst complex essential for exocytosis. Mitotic phosphorylation of Exo84 disrupted the assembly of the exocyst complex, thereby affecting exocytosis and cell surface expansion. Our study demonstrates the coordination between membrane trafficking and cell cycle progression and provides a molecular mechanism by which cell growth is controlled during the cell division cycle.
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页码:97 / 111
页数:15
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