Gemone instability induced by non-coding RNA expression
| Project/Area Number |
21770193
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Molecular biology
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| Research Institution | National Institute of Genetics |
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Principal Investigator |
IIDA Tetsushi National Institute of Genetics, 細胞遺伝研究系, 助教 (60391851)
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| Project Period (FY) |
2009 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2009: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
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| Keywords | ノンコーディングRNA / サイレンシング / RNA干渉 / 分裂酵母 |
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| Research Abstract |
Cryptic transcripts transcribed from everywhere in eukaryotic chromosomes are rapidly degraded by RNA surveillance mechanisms before translation. Defects in RNA surveillance mechanisms result in aberrant accumulation of noncoding RNAs (ncRNAs) and genome instability. Conversely, how excessively transcribed ncRNAs affect genome stability and gene expression is not known. In this study, we developed an artificial ncRNA-expression system of the ura4^+ reporter gene in fission yeast. One of the strongest promoters, nmt1p, induced antisense RNA of the ura4^+ gene and ura4^+ gene silencing. The ncRNA-induced silencing did not associate with hinstone-H3K9 methylation or accumulation of heterochromatin protein, Swi6, at silenced locus. These results suggest that the ncRNA-induced silencing is regulated by different mechanisms from the heterochromatic silencing. However, interestingly, the RNAi machineries involved in heterochromatic silencing were required for not ncRNA-induced silencing but normal growth of cells excessively expressing ncRNAs. This study proposed that the RNAi mechanism contribute to the RNA surveillance and suppression of genome instability.
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Report
(3 results)
Research Products
(3 results)
