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PMID: 12208963 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Flock house virus RNA polymerase is a transmembrane protein with amino-terminal sequences sufficient for mitochondrial localization and membrane insertion.

Journal of virology ·Vol. 76 ·No. 19 ·2002-10-00 ·Pages 9856-67

Miller DJ, Ahlquist P

Abstract

Localization of RNA replication to intracellular membranes is a universal feature of positive-strand RNA viruses. Replication complexes of flock house virus (FHV), the best-studied alphanodavirus, are located on outer mitochondrial membranes in infected Drosophila melanogaster cells and are associated with the formation of membrane-bound spherules, similar to structures found for many other positive-strand RNA viruses. To further study FHV replication complex formation, we investigated the subcellular localization, membrane association, and membrane topology of protein A, the FHV RNA-dependent RNA polymerase, in the yeast Saccharomyces cerevisiae, a host able to support full FHV RNA replication and virion formation. Confocal immunofluorescence revealed that protein A localized to mitochondria in yeast, as in Drosophila cells, and that this mitochondrial localization was independent of viral RNA synthesis. Nycodenz gradient flotation and dissociation assays showed that protein A behaved as an integral membrane protein, a finding consistent with a predicted N-proximal transmembrane domain. Protease digestion and selective permeabilization after differential epitope tagging demonstrated that protein A was inserted into the outer mitochondrial membrane with the N terminus in the inner membrane space or matrix and that the C terminus was exposed to the cytoplasm. Flotation and immunofluorescence studies with deletion mutants indicated that the N-proximal region of protein A was important for both membrane association and mitochondrial localization. Gain-of-function studies with green fluorescent protein fusions demonstrated that the N-terminal 46 amino acids of protein A were sufficient for mitochondrial localization and membrane insertion. We conclude that protein A targets and anchors FHV RNA replication complexes to outer mitochondrial membranes, in part through an N-proximal mitochondrial localization signal and transmembrane domain.

MeSH Terms
Amino Acid Sequence Animals DNA-Directed RNA Polymerases/chemistry Drosophila melanogaster/virology Membrane Proteins/chemistry Mitochondria/chemistry Molecular Sequence Data Nodaviridae/enzymology RNA, Viral/biosynthesis Rabbits Saccharomyces cerevisiae/chemistry Viral Proteins/chemistry
Chemicals
Membrane Proteins RNA, Viral Viral Proteins DNA-Directed RNA Polymerases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Miller David J
Department of Medicine. Institute for Molecular Virology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Ahlquist Paul
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
2002-10-00
Pages
9856-67
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC136485
Subset
IM
Grants
NIGMS NIH HHS · R01 GM035072 · United States
NIGMS NIH HHS · R37 GM035072 · United States
NIGMS NIH HHS · GM35072 · United States
NIAID NIH HHS · K08 AI01770-01 · United States
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