Molecular cloning and cell cycle-dependent expression of mammalian CRM1, a protein involved in nuclear export of proteins

被引:186
|
作者
Kudo, N
Khochbin, S
Nishi, K
Kitano, K
Yanagida, M
Yoshida, M
Horinouchi, S
机构
[1] UNIV TOKYO, GRAD SCH AGR & LIFE SCI, DEPT BIOTECHNOL, BUNKYO KU, TOKYO 113, JAPAN
[2] FAC MED, INST ALBERT BONNIOT, INSERM, U309, LA TRONCHE, FRANCE
[3] TAKEDA CHEM IND LTD, PHARMACEUT DISCOVERY RES DIV, TSUKUBA, IBARAKI 30042, JAPAN
[4] KYOTO UNIV, FAC SCI, DEPT BIOPHYS, SAKYO KU, KYOTO 60601, JAPAN
关键词
D O I
10.1074/jbc.272.47.29742
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crm1 of Schizosaccharomyces pombe, a nuclear protein essential for proliferation and chromosome region maintenance, is a possible target of leptomycin B, an antifungal and antitumor antibiotic with cell cycle-arresting activity, cDNA encoding a human homolog of Crm1 was cloned, Human CRM1 (hCRM1) consisted of 1071 amino acids, of which the sequence showed 52% homology with S. pombe Crm1. hCRM1 weakly complemented the cold sensitive mutation of S. pombe crm1-809, as did S. pombe crm1(+), Overproduction of hCRM1 under the control of a series of nmt1 promoters suppressed cell proliferation in wild-type S. pombe in an expression level-dependent manner, A similar inhibitory effect was also observed for crm1(+). Cells overproducing either hCRM1 or S. pombe Crm1 were distinctly larger than uninduced cells and contained compacted and fragmented nuclei, Furthermore, calcofluor stain ing demonstrated that most of these cells formed two septa per cell and accumulated a large amount of chitin or its related polysaccharides around the septa, Closely similar phenotypes between hCRM1- and S. pombe Crm1-induced cells indicate that the cloned cDNA encodes a functional homolog of S. pombe crm1(+). Northern blot analyses with RNAs isolated from synchronized mammalian cells showed that the expression of mammalian CRM1 was initiated in late G(1) and reached a peak at G(2)/M, although its protein level unchanged during the cell cycle, Transient expression of hCRM1 fused to the green fluorescent protein (GFP) in NIH3T3 cells showed that hCRM1 was localized preferentially in the nuclear envelope and was also detectable in the nucleoplasm and the cytoplasm, A crm1 mutation of S. pombe caused nuclear import of a GFP fusion protein containing a nuclear export signal but no change in the distribution of a GFP fusion protein containing a nuclear localization signal, All of these data suggest that CRM1 is a novel cell-cycle regulated gene that is essential for the nuclear export signal-dependent nuclear export of proteins.
引用
收藏
页码:29742 / 29751
页数:10
相关论文
共 50 条
  • [21] Novel selective inhibitors of nuclear export CRM1 antagonists for therapy in mantle cell lymphoma
    Zhang, Kejie
    Wang, Michael
    Tamayo, Archito T.
    Shacham, Sharon
    Kauffman, Michael
    Lee, John
    Zhang, Liang
    Ou, Zhishuo
    Li, Changping
    Sun, Luhong
    Ford, Richard J.
    Pham, Lan V.
    EXPERIMENTAL HEMATOLOGY, 2013, 41 (01) : 67 - 78
  • [22] Regulation of NT-PGC-1α Subcellular Localization and Function by Protein Kinase A-dependent Modulation of Nuclear Export by CRM1
    Chang, Ji Suk
    Huypens, Peter
    Zhang, Yubin
    Black, Chelsea
    Kralli, Anastasia
    Gettys, Thomas W.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (23) : 18039 - 18050
  • [23] 4-Octyl itaconate reduces influenza A replication by targeting the nuclear export protein CRM1
    Ribo-Molina, Pau
    Weiss, Hauke J.
    Susma, Balasubramanian
    van Nieuwkoop, Stefan
    Persoons, Leentje
    Zheng, Yunan
    Ruzek, Melanie
    Daelemans, Dirk
    Fouchier, Ron A. M.
    O'Neill, Luke A. J.
    van den Hoogen, Bernadette G.
    JOURNAL OF VIROLOGY, 2023, 97 (10)
  • [24] Stimulated expression of mRNAs in activated T cells depends on a functional CRM1 nuclear export pathway
    Schuetz, Sylvia
    Chemnitz, Jan
    Spillner, Christiane
    Frohme, Marcus
    Hauber, Joachim
    Kehlenbach, Ralph H.
    JOURNAL OF MOLECULAR BIOLOGY, 2006, 358 (04) : 997 - 1009
  • [25] Discovery and validation of the nuclear export protein CRM1 (XPO1) as a new target for the treatment of renal cell carcinoma (RCC)
    Wettersten, Hiromi Inoue
    Kauffman, Michael
    Shacham, Sharon
    Landesman, Yosef
    Yang, Joy
    Evans, Christopher
    Weiss, Robert
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (06)
  • [26] Oxidative Stress Inhibits Nuclear Protein Export by Multiple Mechanisms That Target FG Nucleoporins and Crm1
    Crampton, Noah
    Kodiha, Mohamed
    Shrivastava, Sanhita
    Umar, Rehan
    Stochaj, Ursula
    MOLECULAR BIOLOGY OF THE CELL, 2009, 20 (24) : 5106 - 5116
  • [27] CRM1 mediates nuclear export of nonstructural protein 2 from parvovirus minute virus of mice
    Ohshima, T
    Nakajima, T
    Oishi, T
    Imamoto, N
    Yoneda, Y
    Fukamizu, A
    Yagami, K
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 264 (01) : 144 - 150
  • [28] Enhanced nuclear protein export in premature aging and rescue of the progeria phenotype by modulation of CRM1 activity
    Garcia-Aguirre, Ian
    Alamillo-Iniesta, Alma
    Rodriguez-Perez, Ruth
    Velez-Aguilera, Griselda
    Amaro-Encarnacion, Elianeth
    Jimenez-Gutierrez, Elizabeth
    Vasquez-Limeta, Alejandra
    Samuel Laredo-Cisneros, Marco
    Morales-Lazaro, Sara L.
    Tiburcio-Felix, Reynaldo
    Ortega, Arturo
    Magana, Jonathan J.
    Winder, Steve J.
    Cisneros, Bulmaro
    AGING CELL, 2019, 18 (05)
  • [29] Leptomycin B, an inhibitor of the nuclear export receptor CRM1, inhibits COX-2 expression
    Jang, BC
    Muñoz-Najar, U
    Paik, JH
    Claffey, K
    Yoshida, M
    Hla, T
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (05) : 2773 - 2776
  • [30] Cell cycle-dependent phosphorylation of mammalian protein phosphatase 1 by cdc2 kinase
    Kwon, YG
    Lee, SY
    Choi, YW
    Greengard, P
    Nairn, AC
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) : 2168 - 2173