1996 Fiscal Year Final Research Report Summary
Cell cycle regulation of a lympho-hematopoietic specific Rap1GTPase-activating protein, Spa-1 in lymphocyres.
Project/Area Number |
07670367
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Immunology
|
Research Institution | KYOTO UNIVERSITY |
Principal Investigator |
HATTORI Masakazu Kyoto University, Faculty of Medicine, Dept.of Immunology and Cell Biology, Assistant Researcher, 医学研究科, 助手 (40211479)
|
Co-Investigator(Kenkyū-buntansha) |
MINATO Nagahiro Kyoto University, Faculty of Medicine, Dept.of Immunology and Cell Biology, Prof, 医学研究科, 教授 (40137716)
|
Project Period (FY) |
1995 – 1996
|
Keywords | Spa-1 / Rap1 / GAP / cell cycle progression / 11q13.3 |
Research Abstract |
We have cloned a human homologue of mouse Spa-1 gene (SPA-1) which encodes a 130 kDa (p130) cytoplasmic protein with SH3-binding, Rap1GAP.PEST and leucine zipper/coiled coil domains. p130 expressed in a Baculovirus system exhibits a specfic GTPase-activating activity against Rap1. Overexpression of a truncated Spa-1cDNA in NIH3T3 cells apparently disturbed the entry into the cell cycle in the G0-arrested NIH3T3 cells following mitogenic stimulation, suggesting that the protein is critically involved in the cell cycle regulation via the interaction with Rap1. Genomic mapping indicated that Spa-1 is located at the most centromeric region of chromosome 19 in mouse and at the centrimieric neighborhood of CCND1/PRAD1, a presumed BCL1 oncogene, at 11q13.3 in human.
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Research Products
(10 results)