Structural basis for the nuclear export activity of Importin13

EMBO J. 2013 Mar 20;32(6):899-913. doi: 10.1038/emboj.2013.29. Epub 2013 Feb 22.

Abstract

Importin13 (Imp13) is a bidirectional karyopherin that can mediate both import and export of cargoes. Imp13 recognizes several import cargoes, which include the exon junction complex components Mago-Y14 and the E2 SUMO-conjugating enzyme Ubc9, and one known export cargo, the translation initiation factor 1A (eIF1A). To understand how Imp13 can perform double duty, we determined the 3.6-Å crystal structure of Imp13 in complex with RanGTP and with eIF1A. eIF1A binds at the inner surface of the Imp13 C-terminal arch adjacent and concomitantly to RanGTP illustrating how eIF1A can be exported by Imp13. Moreover, the 3.0-Å structure of Imp13 in its unbound state reveals the existence of an open conformation in the cytoplasm that explains export cargo release and completes the export branch of the Imp13 pathway. Finally, we demonstrate that Imp13 is able to bind and export eIF1A in vivo and that its function is essential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus* / genetics
  • Binding Sites / genetics
  • Cell Nucleus / metabolism*
  • Cytoplasm / metabolism
  • Eukaryotic Initiation Factor-1 / chemistry
  • Eukaryotic Initiation Factor-1 / genetics
  • Eukaryotic Initiation Factor-1 / metabolism
  • HeLa Cells
  • Humans
  • Karyopherins / chemistry*
  • Karyopherins / genetics
  • Karyopherins / metabolism*
  • Models, Biological
  • Models, Molecular
  • Nuclear Proteins / metabolism
  • Protein Interaction Domains and Motifs / genetics
  • Protein Interaction Domains and Motifs / physiology
  • Protein Structure, Quaternary
  • Protein Structure, Secondary
  • Protein Transport / genetics

Substances

  • Eukaryotic Initiation Factor-1
  • IPO13 protein, human
  • Karyopherins
  • Nuclear Proteins
  • eukaryotic peptide initiation factor-1A