期刊
SCIENCE
卷 319, 期 5862, 页码 469-472出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1148980
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资金
- NIGMS NIH HHS [R01GM063045-06] Funding Source: Medline
The chromosome passenger complex ( CPC) controls chromosome congression, kinetochore- microtubule attachments, and spindle checkpoint signaling during mitosis. Aurora- B kinase is the catalytic subunit of the CPC. To understand how a single kinase can regulate such diverse events, we have investigated the activation of Aurora- B and describe two distinct activation mechanisms. First, Aurora- B activation in vitro requires two cofactors, telophase disc-60kD ( TD-60) and microtubules. TD-60 is critical to localize both the CPC and Haspin kinase activity to centromeres and thus regulates Aurora- B at several levels. Second, Aurora- B substrates can inhibit kinase activation, and this is relieved by phosphorylation of these substrates by the centromeric kinases Plk1 and Haspin. These regulatory mechanisms suggest models for phosphorylation by Aurora- B of centromeric substrates at unaligned chromosomes and merotelic attachments.
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