A nuclear export signal is essential for the cytosolic localization of the ran binding protein, RanBP1

被引:135
|
作者
Richards, SA [1 ]
Lounsbury, KM [1 ]
Carey, KL [1 ]
Macara, IG [1 ]
机构
[1] UNIV VERMONT, DEPT MICROBIOL MOL GENET, BURLINGTON, VT 05405 USA
来源
JOURNAL OF CELL BIOLOGY | 1996年 / 134卷 / 05期
关键词
D O I
10.1083/jcb.134.5.1157
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RanBP1 is a Ran/TC4 binding protein that can promote the interaction between Ran and beta-importin/beta-karyopherin, a component of the docking complex for nuclear protein cargo. This interaction occurs through a Ran binding domain (RED). Here we show that RanBP1 is primarily cytoplasmic, but the isolated RED accumulates in the nucleus. A region COOH-terminal to the RED is responsible for this cytoplasmic localization. This domain acts heterologously, localizing a nuclear cyclin B1 mutant to the cytoplasm. The domain contains a nuclear export signal that is necessary but not sufficient for the nuclear export of a functional RED. In transiently transfected cells, epitope-tagged RanBP1 promotes dexamethasone-dependent nuclear accumulation of a glucocorticoid receptor-green fluorescent protein fusion, but the isolated RED potently inhibits this accumulation, The cytosolic location of RanBP1 may therefore be important for nuclear protein import. RanBP1 may provide a key link between the nuclear import and export pathways.
引用
收藏
页码:1157 / 1168
页数:12
相关论文
共 50 条
  • [41] Genomic organization, expression, and localization of murine Ran-binding protein 2 (RanBP2) gene
    Fauser, S
    Aslanukov, A
    Roepman, R
    Ferreira, PA
    MAMMALIAN GENOME, 2001, 12 (06) : 406 - 415
  • [42] Genomic organization, expression, and localization of murine Ran-binding protein 2 (RanBP2) gene
    S. Fauser
    A. Aslanukov
    R. Roepman
    P.A. Ferreira
    Mammalian Genome, 2001, 12 : 406 - 415
  • [43] Subnucleolar localization of signal recognition particle RNA and its relationship to the RAN-GTPase nuclear protein import/export pathway
    Politz, J
    Alavian, CN
    Pederson, T
    MOLECULAR BIOLOGY OF THE CELL, 2001, 12 : 104A - 105A
  • [44] Regulation of subcellular localization of the antiproliferative protein Tob by its nuclear export signal and bipartite nuclear localization signal sequences
    Maekawa, M
    Yamamoto, T
    Nishida, E
    EXPERIMENTAL CELL RESEARCH, 2004, 295 (01) : 59 - 65
  • [45] Isolated mammalian and Schizosaccharomyces pombe Ran-binding domains rescue S. pombe sbp1 (RanBP1) genomic mutants
    Novoa, I
    Rush, MG
    D'Eustachio, P
    MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (07) : 2175 - 2190
  • [46] A CRM1-Mediated Nuclear Export Signal Is Essential for Cytoplasmic Localization of Neurogenin 3 in Neurons
    Simon-Areces, Julia
    Acaz-Fonseca, Estefania
    Ruiz-Palmero, Isabel
    Garcia-Segura, Luis-Miguel
    Arevalo, Maria-Angeles
    PLOS ONE, 2013, 8 (01):
  • [47] RANBP1 promotes colorectal cancer progression by regulating pre-miRNA nuclear export via a positive feedback loop with YAP
    Zheng, Dandan
    Cao, Meng
    Zuo, Siyu
    Xia, Xin
    Zhi, Chunchun
    Lin, Yanbing
    Deng, Sitong
    Yuan, Xiaoqin
    ONCOGENE, 2022, 41 (07) : 930 - 942
  • [48] RANBP1 promotes colorectal cancer progression by regulating pre-miRNA nuclear export via a positive feedback loop with YAP
    Dandan Zheng
    Meng Cao
    Siyu Zuo
    Xin Xia
    Chunchun Zhi
    Yanbing Lin
    Sitong Deng
    Xiaoqin Yuan
    Oncogene, 2022, 41 : 930 - 942
  • [49] RanBP1 plays an essential role in directed migration of neural crest cells during development
    Barriga, Elias H.
    Alasaadi, Delan N.
    Mencarelli, Chiara
    Mayor, Roberto
    Pichaud, Franck
    DEVELOPMENTAL BIOLOGY, 2022, 492 : 79 - 86
  • [50] Coordinate regulation/localization of the carbohydrate responsive binding protein (ChREBP) by two nuclear export signal sites: Discovery of a new leucine-rich nuclear export signal site
    Fukasawa, Masashi
    Ge, Qing
    Wynn, R. Max
    Ishii, Seiji
    Uyeda, Kosaku
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (02) : 1166 - 1169