2010 Fiscal Year Final Research Report
Genome-wide analysis of C.elegans JNK cascade
Project/Area Number |
20570181
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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 |
Cell biology
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Research Institution | Nagoya University |
Principal Investigator |
HISAMOTO Naoki Nagoya University, 理学研究科, 准教授 (80283456)
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Project Period (FY) |
2008 – 2010
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Keywords | C.elegans / JNK / RNAi |
Research Abstract |
The JNK MAP kinase (MAPK) pathway plays a pivotal role in the various stress responses of evolutionarily diverse species. In C. elegans, a JNK-like MAPK pathway composed of MLK-1 MAPKKK, MEK-1 MAPKK and KGB-1 MAPK is known to act in a heavy metal stress response. However, the upstream or downstream components of this pathway remain unknown. It has been shown that the KGB-1 pathway is negatively regulated by VHP-1, a dual-specificity MAPK phosphatase, and that mutations defective in the KGB-1 pathway suppress the growth arrest caused by a loss-of-function mutation in the vhp-1 gene. Therefore, we performed genome-wide RNAi screening for vhp-1 suppressor to identify genes functioning in the KGB-1 pathway. As the result, we identified several genes including novel genes as vhp-1 suppressors. In addition, we identified an adaptor protein SHC-1, a protein kinase MAX-2 and a small G protein MIG-2 as upstream factors of MLK-1 and clarified their roles in KGB-1 cascade.
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[Journal Article] LRRK2 modulates vulnerability to mitochondrial dysfunction in Caenorhabditis elegans.2009
Author(s)
Saha S, Guillily MD, Ferree A, Lanceta J, Chan D, Ghosh J, Hsu CH, Segal L, Raghavan K, Matsumoto K, Hisamoto N, Kuwahara T, Iwatsubo T, Moore L, Goldstein L, Cookson M, Wolozin B.
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Journal Title
J.Neurosci. 29
Pages: 9210-9218.
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[Remarks] ホームページ等