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Classical nuclear localization signals:: Definition, function, and interaction with importin α

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 282, Issue 8, Pages 5101-5105

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R600026200

Keywords

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Funding

  1. MRC [MC_U105178939] Funding Source: UKRI
  2. Medical Research Council [MC_U105178939] Funding Source: Medline
  3. NHGRI NIH HHS [R01 HG002898-03, R01 HG002898] Funding Source: Medline
  4. NIGMS NIH HHS [R01 GM058728] Funding Source: Medline
  5. Medical Research Council [MC_U105178939] Funding Source: researchfish

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The best understood system for the transport of macromolecules between the cytoplasm and the nucleus is the classical nuclear import pathway. In this pathway, a protein containing a classical basic nuclear localization signal (NLS) is imported by a heterodimeric import receptor consisting of the beta-karyopherin importin 13, which mediates interactions with the nuclear pore complex, and the adaptor protein importin a, which directly binds the classical NLS. Here we review recent studies that have advanced our understanding of this pathway and also take a bioinformatics approach to analyze the likely prevalence of this system in vivo. Finally, we describe how a predicted NLS within a protein of interest can be confirmed experimentally to be functionally important.

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