Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation

被引:98
作者
Pidoux, AL
Richardson, W
Allshire, RC
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国惠康基金;
关键词
kinetochore; chromatin; centromere; silencing; chromosome segregation;
D O I
10.1083/jcb.200212110
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fission yeast centromeres are composed of two domains: the central core and the outer repeats. Although both regions are required for full centromere function, the central core has a distinct chromatin structure and is likely to underlie the kinetochore itself, as it is associated with centromere-specific proteins. Genes placed within either region are transcriptionally silenced, reflecting the formation of a functional kinetochore complex and flanking centromeric heterochromatin. Here, transcriptional silencing was exploited to identify components involved in central core silencing and kinetochore assembly or structure. The resulting sim (silencing in the middle of the centromere) mutants display severe chromosome segregation defects. sim2(+) encodes a known kinetochore protein, the centromere-specific histone H3 variant Cnp1(CENP-A). sim4(+) encodes a novel essential coiled-coil protein, which is specifically associated with the central core region and is required for the unusual chromatin structure of this region. Sim4 coimmunoprecipitates with the central core component Mis6 and, like Mis6, affects Cnp1(CENP-A) association with the central domain. Functional Mis6 is required for Sim4 localization at the kinetochore. Our analyses illustrate the fundamental link between silencing, chromatin structure, and kinetochore function, and establish defective silencing as a powerful approach for identifying proteins required to build a functional kinetochore.
引用
收藏
页码:295 / 307
页数:13
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