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2013 Fiscal Year Final Research Report

Understanding of molecular mechanism of the assembly of two RecA homologs, Rad51 and Dmc1

Research Project

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Project/Area Number 23247029
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Research Field Molecular biology
Research InstitutionOsaka University

Principal Investigator

SHINOHARA Akira  大阪大学, たんぱく質研究所, 教授 (00252578)

Project Period (FY) 2011-04-01 – 2014-03-31
Keywords組換え / 減数分裂 / ゲノム安定化 / Rad51
Outline of Final Research Achievements

During recombination, homology search between two DNA molecules is a key reaction which is mediated by the RecA homolog Rad51 during mitosis. On the other hand, homology search in meiotic recombination is catalyzed by a collaborative action of two RecA homolog, Rad51 and Dmc1. Both Rad51 and Dmc1 form a filament on the single-stranded DNAs which is regulated in a positive and negative way. We identified a new protein complex containing Psy3, Csm2, Shu1 and Shu2 for Rad51 assembly. We determined a crystal structure of a core component of this complex, Psy3-Csm2. Surprisingly, Psy3-Csm2 shows a structural similarity to Rad51 dimer, although there is little sequence similarity between the proteins. Based on the structure, we propose how the Psy3-Csm2 promotes Rad51 filament on the DNA. This is very novel finding to understand molecular mechanism on how Rad51 mediators facilitate Rad51 filament formation.

Free Research Field

基礎生物学

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Published: 2016-06-03   Modified: 2016-09-08  

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