2011 Fiscal Year Final Research Report
Mechanism to establish cohesion specifically between sister chromatids
Project/Area Number |
22770005
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Genetics/Genome dynamics
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Research Institution | The University of Tokyo |
Principal Investigator |
TAKASHI Sutani 東京大学, 分子細胞生物学研究所, 助教 (30401524)
|
Project Period (FY) |
2010 – 2011
|
Keywords | ゲノム構築 / 再編 / 維持 |
Research Abstract |
Sister chromatids, products of DNA replication, are held together by cohesin complex, which is vital for faithful chromosome segregation. When the cohesion is established, replication-dependent acetylation of a cohesin subunit Smc3 by Eco1 acetylase plays a critical role. In this study, I investigated how the cohesin acetylation is regulated in the cell cycle and how Eco1's function is coupled with DNA replication. Using an antibody specifically recognizing acetylated Smc3, I found the following.(1) Cohesin is deacetylated specifically by Hos1. This deacetylation is important in recycling cohesion complex for the next cell cycle.(2) Efficient acetylation of cohesin in S phase requires the presence of Ctf18-RFC, Ctf4 and Chl1, all of which are implicated in DNA replication. Subsequent analyses suggested that coordinated replication machinery action, particularly lagging strand synthesis, may play an important role in coupling of cohesin acetylation to DNA replication
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