2001 Fiscal Year Final Research Report Summary
Molecular Mechanisms Controlling Multicellular Organization of Plants
Project/Area Number |
10182103
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Research Category |
Grant-in-Aid for Scientific Research on Priority Areas
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Allocation Type | Single-year Grants |
Review Section |
Biological Sciences
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Research Institution | KYOTO UNIVERSITY |
Principal Investigator |
OKADA Kiyotaka Kyoto univ., Grad. Sch. Science, Professor, 大学院・理学研究科, 教授 (50101093)
|
Co-Investigator(Kenkyū-buntansha) |
FUKUDA Hiroo Univ Tokyo, Grad. Sch. Science. Professor, 大学院・理学系研究科, 教授 (10165293)
SHIMAMOTO Ko Nara Institure of Technology and Science, Professor, バイオサイエンス研究科, 教授 (10263427)
MACHIDA Yasunori Nagoya Univ., Grad, Sch. Science. Professor, 大学院・理学研究科, 教授 (80175596)
SUGIYAMA Tatsuo Riken Institutes, Plant science Center. Director, 植物科学研究センター, センター長 (50023453)
NAKAMURA Kenzo Nagoya Univ., Grad Sch. Agriculture, Professor, 大学院・生命農学研究科, 教授 (80164292)
|
Project Period (FY) |
2002
|
Keywords | multiple cellular organism / symposium / homepage / information exchange / workshop / group meeting / newsletter / open symposium |
Research Abstract |
This project aimed to understand the genetic regulatory systems which contribute to make up multi-cellular body of plants. The project was made up of three different research groups : the advisory group, the research group 1 and the research group 2. The research group 1 and 2 aimed to investigate the systems underlying the meristem formation and maintenance and the organ formation, respectively. The advisory group supported the research groups by sponsoring the meetings and workshops gathering the researchers, published newsletters, and organized the project. By the support of the advisory group, the research groups made a progress as briefly described below. 1. Analysis of a root meristem-defective mutant, hlr, showed that it has a mutation in a subunit of proteosome complex. This is a novel observation showing that programmed protein degradation is required for maintaining the root meristem structure and function. 2. Analysis of NPK1, a MAPKKKinase, and its activation factor, NACK1 kinesin-like protein form a complex and promote cell plate formation at the cell division. 3. A set of genes related to the circadian clock of a short-day plant, rice, was examined. 4. By using synchronized cell culture system of Xinnia and the tip-procedure, a large number of genes were identified which are required for vascular cell formation from leaf cells. Genes required for cell autolysis were cloned. 5. A set of genes were identified which respond to sugar. Mutants showing aberrant sugar-response were isolated from nealy 6,000 activation-tagged lines.
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Research Products
(15 results)