Literature DB >> 11106761

Vesicular stomatitis virus matrix protein inhibits host cell gene expression by targeting the nucleoporin Nup98.

J P Rodrigues, D Sitterlin, A Bachi, X Wu, M Wilm, M Carmo-Fonseca, E Izaurralde.   

Abstract

Vesicular stomatitis virus matrix protein (VSV M) has been shown to inhibit both transcription and nucleocytoplasmic transport. We have isolated a mutant form of M, termed M(D), lacking both inhibitory activities. HeLa cells expressing M, but not M(D), accumulate polyadenylated RNAs within the nucleus. Concomitantly, a fraction of M, but not of the M(D) mutant, localizes at the nuclear rim. Additionally, the nucleoporin Nup98 specifically interacts with M but not with M(D). In Nup98(-/-) cells, both the levels of M at the nuclear envelope and its inhibitory effects on host cell-directed expression of reporter genes were significantly reduced. Together, our data demonstrate that VSV M inhibits host cell gene expression by targeting a nucleoporin and primarily blocking nuclear export.

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Year:  2000        PMID: 11106761     DOI: 10.1016/s1097-2765(00)00120-9

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  128 in total

1.  Effects of poliovirus infection on nucleo-cytoplasmic trafficking and nuclear pore complex composition.

Authors:  K E Gustin; P Sarnow
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

2.  Matrix protein and another viral component contribute to induction of apoptosis in cells infected with vesicular stomatitis virus.

Authors:  S A Kopecky; M C Willingham; D S Lyles
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

3.  Multiple vesiculoviral matrix proteins inhibit both nuclear export and import.

Authors:  J M Petersen; L S Her; J E Dahlberg
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

4.  Genomic but not antigenomic hepatitis delta virus RNA is preferentially exported from the nucleus immediately after synthesis and processing.

Authors:  Thomas B Macnaughton; Michael M C Lai
Journal:  J Virol       Date:  2002-04       Impact factor: 5.103

5.  The nucleoporin Nup153 is required for nuclear pore basket formation, nuclear pore complex anchoring and import of a subset of nuclear proteins.

Authors:  T C Walther; M Fornerod; H Pickersgill; M Goldberg; T D Allen; I W Mattaj
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

6.  Inhibition of nuclear import and alteration of nuclear pore complex composition by rhinovirus.

Authors:  Kurt E Gustin; Peter Sarnow
Journal:  J Virol       Date:  2002-09       Impact factor: 5.103

7.  Intranuclear degradation of nonsense codon-containing mRNA.

Authors:  Marc Bühler; Miles F Wilkinson; Oliver Mühlemann
Journal:  EMBO Rep       Date:  2002-07       Impact factor: 8.807

8.  Structural and functional analysis of the interaction between the nucleoporin Nup98 and the mRNA export factor Rae1.

Authors:  Yi Ren; Hyuk-Soo Seo; Günter Blobel; André Hoelz
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-24       Impact factor: 11.205

9.  Vesicular stomatitis virus infection alters the eIF4F translation initiation complex and causes dephosphorylation of the eIF4E binding protein 4E-BP1.

Authors:  John H Connor; Douglas S Lyles
Journal:  J Virol       Date:  2002-10       Impact factor: 5.103

10.  Leader-induced phosphorylation of nucleoporins correlates with nuclear trafficking inhibition by cardioviruses.

Authors:  Frederick W Porter; Ann C Palmenberg
Journal:  J Virol       Date:  2008-12-10       Impact factor: 5.103

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