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2011 Fiscal Year Final Research Report

The splicing factor and diseases caused by its anomaly

Research Project

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Project/Area Number 21550162
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Chemistry related to living body
Research InstitutionOsaka City University

Principal Investigator

INOUE Akira  大阪市立大学, 大学院・医学研究科, 研究員 (50109857)

Co-Investigator(Kenkyū-buntansha) NAKAJIMA Koichi  大阪市立大学, 大学院・医学研究科, 教授 (00227787)
Co-Investigator(Renkei-kenkyūsha) KOJIMA Hirotada  大阪市立大学, 大学院・医学研究科, 助教 (40336772)
Project Period (FY) 2009 – 2011
KeywordsRNA / プロセシング
Research Abstract

(1) s1-1 suppressed cell death induced by anticancer agents. It regu-lated splicing, and produced an antiapoptotic Fas isoform.(2) Association of S1-1 with tumorigenesis was examined by S1-1 immunohistochemistry for 350 cancer tissue sections. However, S1-1 expression showed no correlation with cancer cell types or cancer malignancy.(3) S1-1 was also a transcription factor. It is noteworthy that S1-1 regulates both transcription and splicing.(4) Three nuclear localization sequences, and two sequences that sequester S1-1 into S1-1 nuclear bodies under reduced cellular transcriptional activity were identified in the S1-1 molecule. Manuscripts on these findings are in preparation.

  • Research Products

    (2 results)

All 2011 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Remarks (1 results)

  • [Journal Article] Phospho-Ser727 of STAT3 regulates STAT3 activity by enhancing dephosphory-lation of phospho-Tyr705 largely through TC452011

    • Author(s)
      Ryohei Wakahara, Hiroyuki Kunimoto, Kanae Tanino, Hirotada Kojima, Akira Inoue, Haruo Shintaku and Koichi Nakajima
    • Journal Title

      Genes to Cells

      Volume: 17 Pages: 132-145

    • DOI

      DOI:10.1111/j.1365-2443.2011.01575.x.

    • Peer Reviewed
  • [Remarks] 2009年春までの担当講座

    • URL

      http://www.med.osaka-cu.ac.jp/mmbiore/

URL: 

Published: 2013-07-31  

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