Mechanism of meiotic DNA double strand break formation in chromatin structure
| Project/Area Number |
26440186
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Genetics/Chromosome dynamics
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| Research Institution | Chuo University |
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Principal Investigator |
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| Project Period (FY) |
2014-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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| Keywords | 減数分裂 / 相同組換え / クロマチン / DNA二重鎖切断 |
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| Outline of Final Research Achievements |
Meiotic recombination is initiated by programmed DNA double strand breaks (DSBs) formed at hotspots. Using fission yeast as a model system, we have been studying how DSBs are formed in chromatin structure, and previously reported that acetylated histone H3 lysine 9 (H3K9ac) and the histone H3 lysine 4 methyltransferase Set1 are involved in the event. Here, I have extended our analysis by examining roles of H3K9ac and Set1 and factors cooperating with these factors.
We found that transcription around the model hotspot ade6-3049 promotes H3K9ac at this hotspot. This tendency may be universal, as previously reported data sets suggested that transcripts are found in hotspots-surrounding regions. Our analyses also found that Set1 and the histone H2A.Z activates DSB formation in distinct pathways, and that H2A.Z facilitates DSB formation by modulating chromosome compaction to help DSB-related factors bind to chromatin.
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Report
(5 results)
Research Products
(13 results)
