GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.
PMID:22553322
Citation |
Youn, S, Li, T, McCune, BT, Edeling, MA, Fremont, DH, Cristea, IM and Diamond, MS (2012) Evidence for a genetic and physical interaction between nonstructural proteins NS1 and NS4B that modulates replication of West Nile virus. J. Virol. 86:7360-71 |
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Abstract |
Flavivirus NS1 is a nonstructural glycoprotein that is expressed on the cell surface and secreted into the extracellular space. Despite its transit through the secretory pathway, NS1 is an essential gene linked to early viral RNA replication. How this occurs has remained a mystery given the disparate localization of NS1 and the viral RNA replication complex, as the latter is present on the cytosolic face of the endoplasmic reticulum (ER). We recently identified an N-terminal di-amino acid motif in NS1 that modulates protein targeting and affected viral replication. Exchange of two amino acids at positions 10 and 11 from dengue virus (DENV) into West Nile virus (WNV) NS1 (RQ10NK) changed its relative surface expression and secretion and attenuated infectivity. However, the phenotype of WNV containing NS1 RQ10NK was unstable, as within two passages heterogeneous plaque variants were observed. Here, using a mutant WNV encoding the NS1 RQ10NK mutation, we identified a suppressor mutation (F86C) in NS4B, a virally encoded transmembrane protein with loops on both the luminal and cytoplasmic sides of the ER membrane. Introduction of NS4B F86C specifically rescued RNA replication of mutant WNV but did not affect the wild-type virus. Mass spectrometry and coimmunoprecipitation studies established a novel physical interaction between NS1 and NS4B, suggesting a mechanism for how luminal NS1 conveys signals to the cytoplasm to regulate RNA replication. |
Links |
PubMed PMC3416313 Online version:10.1128/JVI.00157-12 |
Keywords |
Amino Acid Substitution; Animals; Cell Line; Cricetinae; Immunoprecipitation; Mass Spectrometry; Mutant Proteins/genetics; Mutant Proteins/metabolism; Mutation, Missense; Protein Binding; Protein Interaction Mapping; Suppression, Genetic; Viral Nonstructural Proteins/genetics; Viral Nonstructural Proteins/metabolism; Virus Replication; West Nile virus/physiology |
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Significance
Annotations
Gene product | Qualifier | GO Term | Evidence Code | with/from | Aspect | Extension | Notes | Status |
---|---|---|---|---|---|---|---|---|
GO:0045070: positive regulation of viral genome replication |
ECO:0000315: |
P |
Figure 3 and figure 4 for NS4B, but the expt was done in the presence of NS4 F86C mutation, but UniProt doesn't offer separate mature protein record for each component of the polyprotein from WNV. |
complete | ||||
involved_in |
GO:0045070: positive regulation of viral genome replication |
ECO:0000315: mutant phenotype evidence used in manual assertion |
P |
Seeded From UniProt |
complete | |||
See also
References
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