| Project/Area Number |
15370023
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
植物生理・分子
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| Research Institution | Nara Institute of Science and Technology |
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Principal Investigator |
HASHIMOTO Takashi Nara Institute of Science and Technology, Graduate School of Biological Sciences, Professor, バイオサイエンス研究科, 教授 (80180826)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥14,000,000 (Direct Cost: ¥14,000,000)
Fiscal Year 2005: ¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2004: ¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 2003: ¥6,300,000 (Direct Cost: ¥6,300,000)
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| Keywords | MAP kinase / phosphatase / microtubule / twisting / Arabidopsis / cell elongation / 変異株 / 細胞伸長 |
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| Research Abstract |
We isolated a semi-dominant Arabidopsis thaliana mutant propyzamide hypersensitive 1-1 (phs1-1) which showed hypersensitivity toward a microtubule-depolymerizing drug, propyzamide, and demonstrated that PHS1 codes for a novel protein belonging to a mitogen-activated. protein kinase (MAPK) phosphatase family. The phosphatase in phs1-1 had an amino acid exchange at the conserved MAPK-interaction domain at the N-terminus, retained a phosphatase activity, and acted dominant negatively.
Several T-DNA insertion null alleles of PHS1 which lacked expression of the PHS1 protein grew normally and did not show any obvious phenotypic abnormalities. We isolated many genetic suppressors of phs1-1, and found 7 intragenic suppressor alleles of PHS1, further demonstrating that homozygous PHS1 null alleles do not show obvious phenotypes. Other phosphatases may have redundant functions. The suppressor screening also recovered several extragenic suppressor mutants. Some of these extragenic suppressor alleles were found to have mutations in tubulin genes. Responsible genes for the remaining suppressor mutants are being cloned by a map-based approach.
Expression of the PHS gene was analyzed in transgenic Arabidopsis plants in which a GUS reporter gene was inserted in the C-terminus of the PHS1 protein in the genomic region. Basal GUS activities were detected in almost all cell types but the strong expression was observed in rapidly elongating cells. When GFP-PHS1 was expressed under its own promoter and terminator, wild-type PHS1 was found uniformly in the cytosol whereas the phs1-1 version of PHS1 was localized in a dot-like pattern in the cytoplasm.
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