کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6139008 | 1594236 | 2015 | 11 صفحه PDF | دانلود رایگان |
- We used an unbiased proteomics approach to identify RNA-associated proteins during HCMV infection.
- We confirmed changes in abundance and activity for two host RNA-binding proteins, DHX9 and DDX3.
- We identified and confirmed three HCMV-RNA binding proteins during infection, pUS22, pTRS1 and pp71.
- pp71 associated with host and viral mRNAs and associated with polysomes in infected cells, and increased protein synthesis.
Post-transcriptional events regulate herpesvirus gene expression, yet few herpesvirus RNA-binding proteins have been identified. We used an unbiased approach coupling oligo(dT) affinity capture with proteomics to identify viral RNA-associated proteins during infection. Using this approach, we identified and confirmed changes in the abundance or activity of two host RNA-associated proteins, DHX9 and DDX3, in cells infected with human cytomegalovirus (HCMV). We also identified and confirmed previously unreported activities for the HCMV US22 and pp71 proteins as RNA-associated viral proteins and confirmed that a known viral RNA-binding protein, pTRS1, associates with RNA in infected cells. Further, we found that HCMV pp71 co-sedimented with polysomes, associated with host and viral RNAs, and stimulated the overall rate of protein synthesis. These results demonstrate that oligo(dT) affinity capture coupled with proteomics provides a rapid and straightforward means to identify RNA-associated viral proteins during infection that may participate in the post-transcriptional control of gene expression.
Journal: Virology - Volume 481, July 2015, Pages 13-23