Conserved features of cohesin binding along fission yeast chromosomes.

Conserved features of cohesin binding along fission yeast chromosomes.
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DOI:
10.1186/gb-2009-10-5-r52
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发表时间:
2009
期刊:
影响因子:
12.3
通讯作者:
Uhlmann F
Uhlmann F
中科院分区:
生物学1区
文献类型:
--
作者:
Schmidt CK;Brookes N;Uhlmann F

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High-resolution analysis of cohesin localization on fission yeast chromosomes reveals that several determinants, previously thought to be organism-specific, come together to shape overall distribution. Cohesin holds sister chromatids together to enable their accurate segregation in mitosis. How, and where, cohesin binds to chromosomes are still poorly understood, and recent genome-wide surveys have revealed an apparent disparity between its chromosomal association patterns in different organisms. Here, we present the high-resolution analysis of cohesin localization along fission yeast chromosomes. This reveals that several determinants, thought specific for different organisms, come together to shape the overall distribution. Cohesin is detected at chromosomal loading sites, characterized by the cohesin loader Mis4/Ssl3, in regions of strong transcriptional activity. Cohesin also responds to transcription by downstream translocation and accumulation at convergent transcriptional terminators surrounding the loading sites. As cells enter mitosis, a fraction of cohesin leaves chromosomes in a cleavage-independent reaction, while a substantial pool of cohesin dissociates when it is cleaved at anaphase onset. We furthermore observe that centromeric cohesin spreads out onto chromosome arms during mitosis, dependent on Aurora B kinase activity, emphasizing the plasticity of cohesin behavior. Our findings suggest that features that were thought to differentiate cohesin between organisms collectively define the overall behavior of fission yeast cohesin. Apparent differences between organisms might reflect an emphasis on different aspects, rather than different principles, of cohesin action.
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