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1 Department of Botany, University of British Columbia, Vancouver, BC, Canada
2 Pacific Agri-Food Research Centre, 4200 Highway 97, Summerland, BC, Canada V0H 1Z0
Correspondence
Hélène Sanfaçon
SanfaconH{at}agr.gc.ca
The putative NTP-binding protein (NTB) of Tomato ringspot nepovirus (ToRSV) contains a hydrophobic region at its C terminus consisting of two adjacent stretches of hydrophobic amino acids separated by a few amino acids. In infected plants, the NTBVPg polyprotein (containing the domain for the genome-linked protein) is associated with endoplasmic reticulum-derived membranes that are active in ToRSV replication. Recent results from proteinase K protection assays suggested a luminal location for the VPg domain in infected plants, providing support for the presence of a transmembrane domain at the C terminus of NTB. In this study, we have shown that NTBVPg associates with canine microsomal membranes in the absence of other viral proteins in vitro and adopts a topology similar to that observed in vivo in that the VPg is present in the lumen. Truncated proteins containing 60 amino acids at the C terminus of NTB and the entire VPg exhibited a similar topology, confirming that this region of the protein contains a functional transmembrane domain. Deletion of portions of the C-terminal hydrophobic region of NTB by mutagenesis and introduction of glycosylation sites to map the luminal regions of the protein revealed that only the first stretch of hydrophobic amino acids traverses the membrane, while the second stretch of hydrophobic amino acids is located in the lumen. Our results provide additional evidence supporting the hypothesis that the NTBVPg polyprotein acts as a membrane-anchor for the replication complex.
Present address: Southern Crop Protection and Food Research Centre, 1391 Sandford Street, London, Ontario, Canada, N5V 4T3.
Present address: The Hospital for Sick Children, Cancer Research Program, 555 University Avenue, Toronto, Ontario, Canada, M5G 1X8.
This article has been cited by other articles:
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G. Zhang and H. Sanfacon Characterization of Membrane Association Domains within the Tomato Ringspot Nepovirus X2 Protein, an Endoplasmic Reticulum-Targeted Polytopic Membrane Protein J. Virol., November 1, 2006; 80(21): 10847 - 10857. [Abstract] [Full Text] [PDF] |
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S. C. Zhang, G. Zhang, L. Yang, J. Chisholm, and H. Sanfacon Evidence that Insertion of Tomato Ringspot Nepovirus NTB-VPg Protein in Endoplasmic Reticulum Membranes Is Directed by Two Domains: a C-Terminal Transmembrane Helix and an N-Terminal Amphipathic Helix J. Virol., September 15, 2005; 79(18): 11752 - 11765. [Abstract] [Full Text] [PDF] |
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