| Project/Area Number |
11306007
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
応用微生物学・応用生物化学
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| Research Institution | Hokkaido University |
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Principal Investigator |
TOMITA Fusao Hokkaido University, Graduate School of Agriculture, Professor, 大学院・農学研究科, 教授 (60217536)
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| Co-Investigator(Kenkyū-buntansha) |
YASUDA Nobuko National Agriculture Research Center, Researcher, 中央農業研究センター・北陸研究センター, 研究員 (00355504)
NAKAJIMA Toshihiko National Agriculture Research Center, Laboratory Head, 中央農業研究センター・北陸研究センター, 室長 (70355585)
ISHII Chizu Saitama University, Faculty of Science, Associate Professor, 理学部, 助教授 (00114215)
SONE Teruo Hokkaido University, Graduate School of Agriculture, Assistant Professor, 大学院・農学研究科, 助手 (00333633)
TSUJIMOTO Masako National Agriculture Research Center, Researcher, 中央農業研究センター・北陸研究センター, 研究員 (80355586)
犬飼 剛 北海道大学, 大学院・農学研究科, 助手 (90223239)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥40,040,000 (Direct Cost: ¥37,700,000、Indirect Cost: ¥2,340,000)
Fiscal Year 2001: ¥10,140,000 (Direct Cost: ¥7,800,000、Indirect Cost: ¥2,340,000)
Fiscal Year 2000: ¥7,300,000 (Direct Cost: ¥7,300,000)
Fiscal Year 1999: ¥22,600,000 (Direct Cost: ¥22,600,000)
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| Keywords | Avirulence genes / Magnaporthe grisea / Recombinational repair / RAD52 / RAD54 / MRE11 / Neurospora crassa / Mutation / Avirulence gene / Neurospora crassa / トランスポゾン / RFLP / Mre11 / Magnaporthe / いもち病 / AFLP / PCR / 変異株 / 組み換え |
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| Research Abstract |
(1) Analysis of avirulence genes in M. grisea
Three avirulence genes, Avr-pii, Avr-pia, Avr-Hattan3 was investigated using a cross between two Yunnang isolates. These avirulence genes were mapped onto the genetic map of the fungus. Along the Avr-Hattan 3, a BAC contig of 600kb in length was constructed. On the other hand, Avr-pia was identified also from a cross between Japanese isolate and rare hermaphloditic isolate Guy11. By utilization of the host specificity mutant, a DNA fragment named PM-01, which was tightly linked to the Avr-pia locus was isolated. One of the cosmid clone containing the PM-01 fragment was found to be able to complement the host specificity mutation, indicating that the clone containing the Avr-pia gene.
(2) Analysis of recombnational repair genes in M. grisea
Homologous genes for RAD52, RAD54, and MRE11 was cloned from M. grisea genome, and named Rhm52, Rhm54 and Mhm11, respectively. Among these homologs, Rhm54 was found to complement the phenotype of mus-23 mutant of N. crassa, and to be inducible by MMS treatment in M. grisea cells.
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