Ipl1p-dependent phosphorylation of Mad3p is required for the spindle checkpoint response to lack of tension at kinetochores

被引:57
作者
King, Emma M. J.
Rachidi, Najma
Morrice, Nick
Hardwick, Kevin G.
Stark, Michael J. R.
机构
[1] Univ Dundee, Wellcone Trust Bioctr Complex, Med Sci inst, Coll Life Sci,Div Gene Regualt & Express, Dundee DD1 5EH, Scotland
[2] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Univ Dundee, Wellcone Trust Bioctr Complex, Med Sci inst, Coll Life Sci,Med Res Council Prot Phosphorylat U, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
Mad3; Aurora kinase; tension; spindle checkpoint;
D O I
10.1101/gad.431507
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The spindle checkpoint delays anaphase onset until all chromosomes are correctly attached to microtubules. Ipl1 protein kinase (Aurora B) is required to correct inappropriate kinetochore-microtubule attachments and for the response to lack of tension between sister kinetochores. Here we identify residues in the checkpoint protein Mad3p that are phosphorylated by Ipl1p. When phosphorylation of Mad3p at two sites is prevented, the cell's response to reduced kinetochore tension is dramatically curtailed. Our data provide strong evidence for a distinct checkpoint pathway responding to lack of sister kinetochore tension, in which Ipl1p-dependent phosphorylation of Mad3p is a key step.
引用
收藏
页码:1163 / 1168
页数:6
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