Abstract

The GTPase Ran/TC4 and the 14-kDa protein nuclear transport factor 2 (NTF2) are two of the cytosolic factors that mediate nuclear protein import in vertebrates. Previous biochemical studies have shown that NTF2 binds directly to the GDP-bound form of Ran/TC4 and to proteins of the nuclear pore complex that contain phenylalanine-glycine repeats. In the present study we have used molecular genetic approaches to study the Saccharomyces cerevisiae homologue of NTF2. The scNTF2 gene encodes a protein that is 44% identical to the human protein. We found that deletion of the scNTF2 gene is lethal and that repression of NTF2p expression by a regulatable promoter results in gross structural distortions of the nuclear envelope. In a screen for high copy number suppressors of a scNTF2 deletion, the only gene we isolated other than scNTF2 itself was GSP1, the S. cerevisiae homologue of Ran/TC4. Furthermore, we found that high levels of Ran/TC4 can relieve the requirement for NTF2 in a mammalian-permeabilized cell assay for nuclear protein import. These data suggest that certain of the nuclear protein import functions of NTF2 and Ran/TC4 are closely linked and that NTF2 may serve to modulate a transport step involving Ran/TC4.

Highlights

  • Exchange of macromolecules between the cytoplasm and nucleus is specified by signals encoded within transported proteins

  • A group of cytosolic factors that mediate nuclear import of proteins containing these basic-type nuclear localization signals (NLSs) has been identified. These include the ␣ subunit of the NLS receptor (␣ importin/␣ karyopherin; Refs. 2– 4) and its ␤ subunit (p97/␤ importin/␤ karyopherin; Refs. 5–7), the GTPase Ran/TC4 [8, 9], and the homodimeric protein nuclear transport factor 2 (NTF2/ p10; Refs. 10 and 11)

  • We have found that the scNTF2 gene is required for viability and that depletion of scNTF2p leads to nuclear structure defects similar to those observed with mutants of certain nuclear pore complex proteins

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Summary

Introduction

Exchange of macromolecules between the cytoplasm and nucleus is specified by signals encoded within transported proteins. A group of cytosolic factors that mediate nuclear import of proteins containing these basic-type NLSs has been identified These include the ␣ subunit of the NLS receptor According to current working models [1, 12], the pathway for import of proteins with basic-type NLSs begins in the cytoplasm, where the ␣ subunit of the receptor binds to the NLS of a protein destined for import. This complex binds to the cytoplasmic surface of the nuclear pore complex (NPC) via the ␤ subunit, an event that is referred to as the initial binding or docking step of transport. These data support the hypothesis that NTF2 serves to modulate a transport step(s) involving Ran/TC4

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