首页    期刊浏览 2024年10月04日 星期五
登录注册

文章基本信息

  • 标题:Specific Y14 domains mediate its nucleo-cytoplasmic shuttling and association with spliced mRNA
  • 本地全文:下载
  • 作者:Naoyuki Kataoka ; Michael D. Diem ; Mayumi Yoshida
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2011
  • 卷号:1
  • DOI:10.1038/srep00092
  • 出版社:Springer Nature
  • 摘要:

    Pre-mRNA splicing deposits multi-protein complexes, termed exon junction complexes (EJCs), on mRNAs near exon-exon junctions. The core of EJC consists of four proteins, eIF4AIII, MLN51, Y14 and Magoh. Y14 is a nuclear protein that can shuttle between the nucleus and the cytoplasm, and binds specifically to Magoh. Here we delineate a Y14 nuclear localization signal that also confers its nuclear export, which we name YNS. We further identified a 12-amino-acid peptide near Y14’s carboxyl terminus that is required for its association with spliced mRNAs, as well as for Magoh binding. Furthermore, the Y14 mutants, which are deficient in binding to Magoh, could still be localized to the nucleus, suggesting the existence of both the nuclear import pathway and function for Y14 unaccompanied by Magoh.

    .

    © 2011 Macmillan Publishers Limited. All rights reserved

国家哲学社会科学文献中心版权所有