The study of the synaptonemal complex component SYCP3 in meiotic recombination
Project/Area Number |
16H07295
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Genome biology
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Research Institution | Waseda University |
Principal Investigator |
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Project Period (FY) |
2016-08-26 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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Keywords | 相同組換え / シナプトネマ複合体 / SYCP3 / RAD51 / DMC1 / 相同的対合 / 減数分裂期組換え / 相同的対合反応 |
Outline of Final Research Achievements |
The purpose of this study is to elucidate the molecular mechanism of meiotic recombination by the synpatonemal complex component SYCP3. The synaptonemal complex is essential for the progression of meiotic recombination. However, the functions of SYCP3 in meiotic recombination remain elusive. We performed the biochemical and cell biology analyses to elucidate the mechanism by which SYCP3 regulates RAD51- and DMC1- homologous pairing. We found that SYCP3 significantly suppresses the RAD51-mediated homologous pairing, but not DMC1-mediated homologous pairing. In addition, we found that SYCP3 specifically binds to RAD51 and suppresses RAD51-mediated homologous pairing by competing with HOP2-MND1 complex.
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Report
(3 results)
Research Products
(12 results)
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[Journal Article] Replication stress induces accumulation of FANCD2 at central region of large fragile genes.2018
Author(s)
Okamoto Y, Iwasaki WM, Kugou K, Takahashi KK, Oda A, Sato K, Kobayashi W, Kawai H, Sakasai R, Takaori-Kondo A, Yamamoto T, Kanemaki MT, Taoka M, Isobe T, Kurumizaka H, Innan H, Ohta K, Ishiai M, Takata M.
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Journal Title
Nucleic Acids Res.
Volume: 46(6)
Issue: 6
Pages: 2932-2944
DOI
NAID
Related Report
Peer Reviewed / Open Access
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