The Karyopherin-β family of proteins mediates nuclear transport of macromolecules. Nuclear versus cytoplasmic localization of proteins is often suggested by the presence of NLSs (nuclear localization signals) or NESs (nuclear export signals). Import-Karyopherin-βs or Importins bind to NLSs in their protein cargos to transport them through nuclear pore complexes into the nucleus. Until recently, only two classes of NLS had been biochemically and structurally characterized: the classical NLS, which is recognized by the Importin-α/β heterodimer and the PY-NLS (proline–tyrosine NLS), which is recognized by Karyopherin-β2 or Transportin-1. Structures of two other Karyopherin-βs, Kap121 and Transportin-SR2, in complex with their respective cargos were reported for the first time recently, revealing two new distinct classes of NLSs. The present paper briefly describes the classical NLS, reviews recent literature on the PY-NLS and provides in-depth reviews of the two newly discovered classes of NLSs that bind Kap121p and Transportin-SR respectively.
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June 2015
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Review Article|
June 15 2015
Nuclear localization signals for four distinct karyopherin-β nuclear import systems
Michael Soniat
;
Michael Soniat
*Department of Pharmacology, University of Texas Southwestern, Dallas, TX 75390, U.S.A.
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Yuh Min Chook
Yuh Min Chook
1
*Department of Pharmacology, University of Texas Southwestern, Dallas, TX 75390, U.S.A.
1To whom correspondence should be addressed (email yuhmin.chook@utsouthwestern.edu).
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Biochem J (2015) 468 (3): 353–362.
Article history
Received:
March 24 2015
Revision Received:
April 16 2015
Accepted:
April 20 2015
Citation
Michael Soniat, Yuh Min Chook; Nuclear localization signals for four distinct karyopherin-β nuclear import systems. Biochem J 15 June 2015; 468 (3): 353–362. doi: https://doi.org/10.1042/BJ20150368
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