Project/Area Number |
08408031
|
Research Category |
Grant-in-Aid for Scientific Research (A)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Molecular biology
|
Research Institution | KYOTO UNIVERSITY |
Principal Investigator |
OKADA Kiyotaka KYOTO UNIVERSITY,Grad.Sch.Sci., Professor, 大学院・理学研究科, 教授 (50101093)
|
Co-Investigator(Kenkyū-buntansha) |
ISHIGURO Sumie KYOTO UNIVERSITY,Grad.Sch.Sci., Research Associate, 大学院・理学研究科, 助手 (50260039)
|
Project Period (FY) |
1996 – 1998
|
Project Status |
Completed (Fiscal Year 1998)
|
Budget Amount *help |
¥29,900,000 (Direct Cost: ¥29,900,000)
Fiscal Year 1998: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1997: ¥10,000,000 (Direct Cost: ¥10,000,000)
Fiscal Year 1996: ¥17,200,000 (Direct Cost: ¥17,200,000)
|
Keywords | PLANT ORGANOGENESIS / CELL DIFFERENTIATION / INTERCELLULAR SIGNALING / ARABIDOPSIS / MUTANT ANALYSIS / ROOT HAIR FORMATION / TRANSCRIPTION FACTOR / FLOWER DEVELOPMENT / 表裏の軸決定 / 接触刺激 / プラズモデデスマ-タ / トランスジェニック植物 / mybドメイン / プラズモデスマ-タ |
Research Abstract |
This project aimed to clarify intercellular signaling mechanism in plant organogenesis using several mutants of Arabidopsis. Major results obtained in the 3-year project are : (1) We identified and cloned a positive regulator, CPC, promoting differentiation of the root hair cells. CPC encodes a small myb protein, and found to be expressed in non-hair cells. It is strongly suggested that CPC protein moves to the neighboring hair cells. (2) HY5 gene was shown to have a role in photomorphogenesis, cell elongation, cell division, and chloroplast development. We cloned HY5 and found it encodes a bZIP protein, and associates with other photomorphogenesis regulatory proteins COP1 and DET1. (3) We cloned a flower gene, FIL, and found it encodes a protein with a zinc-finger and a HMG-related domains. FIL was expressed at the abaxial side tissues of leaves and of floral organs. Transgenic plants showed FIL has a role in determination of the abaxial side of lateral organs. (4) We identified a mutant with aberrant structure in meristems, L12, has two mutations. One gene, L12a, was found to encode a HSP90-related protein.
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