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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Active Transport, Cell Nucleus
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Amino Acid Sequence
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Animals
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Cell Line
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Cell Nucleus / genetics
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Cell Nucleus / metabolism*
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Gene Expression Regulation*
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HeLa Cells
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Humans
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Mice
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Mice, Knockout
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Molecular Sequence Data
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Mutation / genetics
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Nuclear Pore / chemistry
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Nuclear Pore / metabolism
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Nuclear Pore Complex Proteins / chemistry
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Nuclear Pore Complex Proteins / deficiency
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Nuclear Pore Complex Proteins / genetics
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Nuclear Pore Complex Proteins / metabolism*
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Protein Binding
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Protein Structure, Tertiary
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Repetitive Sequences, Amino Acid
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Substrate Specificity
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Transcription, Genetic
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Viral Matrix Proteins / chemistry
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Viral Matrix Proteins / genetics
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Viral Matrix Proteins / metabolism*
Substances
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M protein, Vesicular stomatitis virus
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Nuclear Pore Complex Proteins
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RNA, Messenger
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Viral Matrix Proteins
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nuclear pore complex protein 98