Cloning and characterization of human karyopherin β3

  1. Nabeel R. Yaseen*, and
  2. Günter Blobel*,
  1. *Laboratory of Cell Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021; and Department of Pathology, Cornell University Medical College, New York, NY 10021

Abstract

Nuclear import of classical nuclear localization sequence-bearing proteins is mediated by karyopherin α/β1 heterodimers. A second nuclear import pathway, mediated by karyopherin β2 (transportin), recently was described for mRNA-binding proteins. Here we report the cloning and characterization of human karyopherin β3, which may be involved in a third pathway for nuclear import. Karyopherin β3 was localized mainly to the cytosol and the nucleus, particularly the nuclear rim. It bound to several of the repeat-containing nucleoporins (Nup358, Nup214, Nup153, Nup98, and p62) in overlay and solution-binding assays and was competed away by karyopherin β1. For Nup98, we localized this binding to the peptide repeat-containing region. Karyopherin β3 contains two putative Ran-binding homology regions and bound to Ran-GTP in a solution-binding assay with much higher affinity than to Ran-GDP. Furthermore, it interacted with two ribosomal proteins in an overlay assay. We suggest that karyopherin β3 is a nuclear transport factor that may mediate the import of some ribosomal proteins into the nucleus.

Footnotes

  • To whom reprint requests should be addressed. e-mail: blobel{at}rockvax.rockefeller.edu.

  • Günter Blobel

  • Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. BankIt71891 U72761U72761).

  • ABBREVIATIONS:
    EST,
    expressed sequence tag;
    TBS-T,
    20 mM Tris/137 mM NaCl/0.1% Tween 20;
    TB-T/milk,
    transport buffer/0.1% Tween 20/5% milk;
    GST,
    glutathione S-transferase
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