Analysis of Wnt signaling pathway mediated frizzled protein family
| Project/Area Number |
13680795
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Cell biology
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| Research Institution | Japanese Foundation for Cancer Research |
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Principal Investigator |
YAO Ryoji The JFCR-Cancer Institute, Dept Cell Blol. Researcher, 癌研究所・細胞生物部, 研究員 (80291095)
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| Project Period (FY) |
2001 – 2002
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| Project Status |
Completed (Fiscal Year 2002)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2002: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2001: ¥2,500,000 (Direct Cost: ¥2,500,000)
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| Keywords | frizzled / Wnt / GOPC / veslcle transport / wnt / Vesicle transport / PDZ domain / 細胞分裂 |
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| Research Abstract |
Frizzled proteins play a role as a Wnt receptor and involved in the regulation of gene expression as well as planar cell polarity. Since carboxyl temini of many frizzled family members contain PDZ binding motifs, we isolated several candidate molecules that potentially interact with frizzled.
One of these interacting proteins, fzip-1 , contains two coiled-coil motif and one PDZ domain. This molecule was named as Golgi-associated PDZ and coiled-coil motif containing protein (GOPC), as it was localized at the Golgi apparatus. A series of molecular studies indicates GOPC has a role in transport of frizzled form the Golgi apparatus to plasma membrane. Furthermore, Male GOPC knockout mouse was infertile due to abnormal acrosome formation. Electronmicrosopic analysis revealed that vesicle transport from the Golgi apparatus to acrosome was severely impaired. Thus it appears GOPC functions the vesicle transport to acrosome in addition to plasma membrane. We also found that the second interacting molecule; fzip-2, is involved in G protein dependent -JNK activation, whereas the third molecule, fzip-3, is suggested to function in cell division. We are currently investigating the molecular analysis of these molecules as well as their biological significance by gene targeting.
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Report
(3 results)
Research Products
(7 results)
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[Publications] Yao, R., Ito, T., Natsume, Y., Sugitani, Y., Yamanaka, H., Kuretake, S., Yanagida, K., Sato, A., Toshimori, K., Noda, T.: "Lack of acrosome formation in mice lacking a Golgi protein, GOPC"Proc.Natl.Acad.Sci., U.S.A.. 99. 11211-11216 (2002)
Description
「研究成果報告書概要(和文)」より
Related Report
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[Publications] Yao, R. Ito, C. Natsume, Y. Sugitani, Y. Yamanaka, H. Kuretake, S. Yanagida, K. Sato, A. Toshimori, K. and Noda, T.: "Lack of acrosome formation in mice lacking a Golgi protein,GOPC."Proc. Natl.Acad, Sci., U.S.A.. 99. 11211-11216 (2002)
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Publications] Yao, R., Ito, C., Natsume, Y., Sugitani, Y., Yamanaka, H., Kuretake, S., Yanagida, K., Sato, A., Toshimori, K., Noda, T.: "Lack of acrosome formation in mice lacking a Golgi protein, GOPC"Proc.Natl.Acad.Sci., U.S.A.. 99. 11211-11216 (2002)
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