Thlo modification of yeast cytosolic tRNA is an iron-sulfur protein-dependent pathway
| Project/Area Number |
17570121
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Functional biochemistry
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| Research Institution | Osaka Medical College |
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Principal Investigator |
NAKAI Yumi Osaka Medical College, Faculty of Medicine, Assistant Professor, 医学部, 講師 (80268193)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2005: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | tRNA modification / yeast / mitochondria / cytosol / iron-sulfur cluster / cysteine desulfurase / Hela / sulfur / tRNA修飾 / システインデスルフラーゼ / Nfs1p / チオ修飾 / ミトコンドリアさ / 硫黄原子 |
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| Research Abstract |
Defects in yeast cysteine desulfurase, Nfs1p cause a severe impairment in 2-thio modification of uridine of the mitochondrial (mt-) tRNAs and the cytosolic (cy-) tRNAs. Nfs1 p can also provide the sulfur atoms of the iron-sulfur (Fe/S) clusters generated by the mitochondrial and cytosolic Fe/S cluster assembly machineries termed ISC and CIA, respectively. Therefore, a key question remains as to whether biosynthesis of Fe/S clusters is a prerequisite for the 2-thio modification of tRNAs in both subcellular compartments of yeast cells. To elucidate this question, we asked if mitochondrial ISC and/or cytosolic CIA components except Nfs1p would be involved in 2-thio modification of these tRNAs. We demonstrate here that the three CIA components, Cfd1p, Nbp35p, and Cia1p, are required for the 2-thio modification of cy-tRNAs but not of mt-tRNAs. Interestingly, the mitochondrial scaffold proteins lsu1p and Isu2p are required to the 2-thio modification of the cytosolic tRNAs but not of the mitochondrial tRNAs while mitochondrial Nfs1p is required for both 2-thio modifications. These results clearly indicate that the 2-thio modification of cytosolic tRNAs is Fe/S protein-dependent and thus requires both CIA and ISC machineries but that of mitochondrial tRNAs is Fe/S cluster-independent and does not require key mitochondrial ISC components except Nfs1p.
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Report
(3 results)
Research Products
(4 results)
