2005 Fiscal Year Final Research Report Summary
basic research oriented for the gene therapy using of newly identified tumor suppressor human Scribble.
Project/Area Number |
16591645
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Obstetrics and gynecology
|
Research Institution | The University of Tokyo |
Principal Investigator |
NAKAGAWA Shunsuke The University of Tokyo, Faculty of Medicine, Research Associate, 医学部附属病院, 助手 (70270874)
|
Co-Investigator(Kenkyū-buntansha) |
YANO Tetsu The University of Tokyo, Faculty of Medicine, Associate Professor, 医学部附属病院, 助教授 (90251264)
|
Project Period (FY) |
2004 – 2005
|
Keywords | tumor suppressor / cell polarity / human papillomavirus / E6 oncoprotein / ubiquitin-mediated degradation / ubiquitin protein ligase / cell cycle / growth inhibition |
Research Abstract |
Drosophila tumor suppressor Scribble was identified as an apical-basolateral polarity determinant in epithelia. Human homologue of Drosophila Scribble, human Scribble (hScrib), has been identified as a protein targeted by human papillomavirus E6 for the ubiquitin-mediated degradation depending on E6AP, a cellular ubiquitin-protein ligase. Human Scribble is classified as a LAP protein, having leucine-rich repeats (LRRs) and PDZ domains. We investigated whether hScrib, which is thought to have a role in polarity determination based on the data of its Drosophila homologue, is involved in cell-cycle regulation and proliferation control of epithelia. Transfection of hScrib suppresses cell proliferation by blocking cell-cycle progression from G1 to S phase. We explored functional domain mapping to reveal which domains of hScrib are critical for its cellular proliferation control and localization at the basolateral membrane. We found that LRRs and PDZ domain 1 are indispensable for hScrib to inhibit cell growth by blocking cell-cycle progression and keep its proper localization. These data indicate that basolateral membrane localization of hScrib is closely related to its proliferation control. Our findings suggest the possibility that hScrib is involved in signal transduction to negatively regulate cell proliferation by localizing at basolateral membrane of epithelial cells through LRRs and PDZ domains.
|
-
[Journal Article] Human Scribble, a novel tumor suppressor identified as a target of high-risk HPV E6 for ubiquitin-mediated degradation, interacts with adenomatous polyposis coli2006
Author(s)
Takizawa S, Nagasaka K, Nakagawa S, Yano T, Matsumoto Y, Nakagawa K, Minaguchi T, Oda K, Hiraike-Wada O, Ooishi H, Matsumoto K, Yasugi T, Taketani Y
-
Journal Title
Genes to Cells. 2006 11
Pages: 453-464
Description
「研究成果報告書概要(和文)」より
-
[Journal Article] Involvement of a cellular ubiquitin-protein ligase E6AP in the ubiquitin-mediated degradation of extensive substrates of high-risk human papillomavirus E6.2006
Author(s)
Matsumoto Y, Nakagawa S, Yano T, Takizawa S, Nagasaka K, Nakagawa K, Minaguchi T, Wada O, Ooishi H, Matsumoto K, Yasugi T, Kanda T, Huibregtse JM, Taketani Y.
-
Journal Title
J Med Virol. 78(4)
Pages: 501-507
Description
「研究成果報告書概要(和文)」より
-
[Journal Article] The DNA mismatch repair gene hMSH2 is a potent coactivator of oestrogen receptor alpha2005
Author(s)
Wada-Hiraike O, Yano T, Nei T, Matsumoto Y, Nagasaka K, Takizawa S, Oishi H, Arimoto T, Nakagawa S, Yasugi T, Kato S, Taketani Y.
-
Journal Title
Br J Cancer. 2005 92(12)
Pages: 2286-91
Description
「研究成果報告書概要(和文)」より
-
-
[Journal Article] The DNA mismatch repair gene hMSH2 is a potent coactivator of oestrogen receptor alpha2005
Author(s)
Wada-Hiraike O, Yano T, Nei T, Matsumoto Y, Nagasaka K, Takizawa S, Oishi H, Arimoto T, Nakagawa S, Yasugi T, Kato S, Taketani Y.
-
Journal Title
Br J Cancer 92(12)
Pages: 2286-2291
Description
「研究成果報告書概要(欧文)」より
-
[Journal Article] Human Scribble, a novel tumor suppressor identified as a target of high-risk HPV E6 for ubiquitin-mediated degradation, interacts with adenomatous polyposis coli2005
Author(s)
Takizawa S, Nagasaka K, Nakagawa S, Yano T, Matsumoto Y, Nakagawa K, Minaguchi T, Oda K, Hiraike-Wada O, Ooishi H, Matsumoto K, Yasugi T, Taketani Y
-
Journal Title
Genes to Cells.
Pages: 453-464
Description
「研究成果報告書概要(欧文)」より
-
-