Literature DB >> 9182759

A distinct nuclear import pathway used by ribosomal proteins.

M P Rout1, G Blobel, J D Aitchison.   

Abstract

Protein transport into the nucleus is governed by the interaction of soluble transport factors with their import substrates and nuclear pore complexes. Here, we identify a major distinct nuclear import pathway, mediated by a previously uncharacterized yeast beta karyopherin Kap123p. The predominant substrates for this pathway are ribosomal proteins, which must be imported into the nucleus prior to assembly into pre-ribosomes. Kap123p binds directly to its transport substrates, repeat motif-containing nucleoporins, and Ran-GTP. We show that the related protein Pse1p is also a karyopherin and can functionally substitute for Kap123p; both are capable of specifically directing a ribosomal nuclear localization signal reporter to the nucleus in vivo.

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Year:  1997        PMID: 9182759     DOI: 10.1016/s0092-8674(00)80254-8

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  149 in total

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8.  Ran-binding protein 5 (RanBP5) is related to the nuclear transport factor importin-beta but interacts differently with RanBP1.

Authors:  R Deane; W Schäfer; H P Zimmermann; L Mueller; D Görlich; S Prehn; H Ponstingl; F R Bischoff
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

9.  In yeast, the 3' untranslated region or the presequence of ATM1 is required for the exclusive localization of its mRNA to the vicinity of mitochondria.

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10.  The importin beta/importin 7 heterodimer is a functional nuclear import receptor for histone H1.

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Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

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