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

被引:106
作者
Miller, DJ
Ahlquist, P
机构
[1] Univ Wisconsin, Inst Mol Virol, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med, Madison, WI 53706 USA
[3] Univ Wisconsin, Howard Hughes Med Inst, Madison, WI 53706 USA
关键词
D O I
10.1128/JVI.76.19.9856-9867.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:9856 / 9867
页数:12
相关论文
共 63 条
[1]  
Ball LA, 1998, VIRUSES, P225
[2]   REQUIREMENTS FOR THE SELF-DIRECTED REPLICATION OF FLOCK HOUSE VIRUS-RNA-1 [J].
BALL, LA .
JOURNAL OF VIROLOGY, 1995, 69 (02) :720-727
[3]   BOOLARRA VIRUS - ULTRASTRUCTURE OF INTRACYTOPLASMIC VIRUS FORMATION IN CULTURED DROSOPHILA CELLS [J].
BASHIRUDDIN, JB ;
CROSS, GF .
JOURNAL OF INVERTEBRATE PATHOLOGY, 1987, 49 (03) :303-315
[4]  
BONIFACINO JS, 2000, CURRENT PROTOCOLS CE
[5]   The 5'-terminal region of a tombusvirus genome determines the origin of multivesicular bodies [J].
Burgyan, J ;
Rubino, L ;
Russo, M .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :1967-1974
[6]   STRUCTURE AND FUNCTION OF CYTOCHROME-C-OXIDASE [J].
CAPALDI, RA .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :569-596
[7]   Brome mosaic virus polymerase-like protein 2a is directed to the endoplasmic reticulum by helicase-like viral protein 1a [J].
Chen, JB ;
Ahlquist, P .
JOURNAL OF VIROLOGY, 2000, 74 (09) :4310-4318
[8]   Yeast-enhanced green fluorescent protein (yEGFP): A reporter of gene expression in Candida albicans [J].
Cormack, BP ;
Bertram, G ;
Egerton, M ;
Gow, NAR ;
Falkow, S ;
Brown, AJP .
MICROBIOLOGY-UK, 1997, 143 :303-311
[9]   Prediction of transmembrane alpha-helices in prokaryotic membrane proteins: the dense alignment surface method [J].
Cserzo, M ;
Wallin, E ;
Simon, I ;
vonHeijne, G ;
Elofsson, A .
PROTEIN ENGINEERING, 1997, 10 (06) :673-676
[10]   Identification of sequences in brome mosaic virus replicase protein 1a that mediate association with endoplasmic reticulum membranes [J].
den Boon, JA ;
Chen, JB ;
Ahlquist, P .
JOURNAL OF VIROLOGY, 2001, 75 (24) :12370-12381