2010 Fiscal Year Final Research Report
Analyses and applications of novel mechanism of phospho-independent regulation of lipid metabolism by Trypanosoma brucei 14-3-3
Project/Area Number |
20590434
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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 |
Parasitology (including Sanitary zoology)
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Research Institution | Kurume University |
Principal Investigator |
INOUE Masahiro Kurume University, 医学部, 教授 (00232562)
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Project Period (FY) |
2008 – 2010
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Keywords | 脂質代謝 / 蛋白リン酸化酵素 / 結合蛋白 / ブルーストリパノソーマ / 2014 / 03 / 03 |
Research Abstract |
Trypanosoma brucei is a causative agent of sleeping sickness. More than 30,000 infected patients died of this devastating disease. One of the aims for this research is to identify the molecular mechanisms by which T. brucei 14-3-3s control the motility, cytokinesis, and cell cycle focusing on the lipid metabolism controlled by Tb14-3-3s as we discovered. We found that Tb14-3-3s interact with the enzymes involved in sugar or lipid metabolism, and protein kinases. One of the protein kinases among them is found out to be critical for the regulation of the motility, cytokinesis and cell cycle.
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Research Products
(9 results)
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[Journal Article] Mutant p53 disrupts the stress MAPK activation circuit induced by ASK1-dependent stabilization of Daxx.2009
Author(s)
Kitamura T., Fukuyo Y., Inoue M., Horikoshi NT., Shindoh, M., Rogers BE., Usheva, A., Horikoshi, N.
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Journal Title
Cancer Res. 69(19)
Pages: 7681-7688
Peer Reviewed
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