期刊
GENOME RESEARCH
卷 14, 期 10B, 页码 2029-2033出版社
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gr.2583304
关键词
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Although cloned viral ORFeomes are particularly well suited for genome-wide interaction mapping due to the limited size of viral genomes, only a few such studies have been published. Here, we summarize virus interaction mapping projects involving vaccinia virus, hepatitis C virus (HCV), potato virus A (PVA), pea seed-borne mosaic: virus (PSbMV), and bacteriophage T7, as well as some projects in progress. The studies reported suggest that: virus-specific coding and replication strategies must be taken into account to yield accurate numbers of protein interactions. In particular, the number of false negatives call be significant for RNA viruses expressing precursor polyproteins (because interactions between full-length mature protein!; are often not detected due to incorrect processing) and for viruses replicating in the cytoplasm whose transcripts have not been selected for splicing signals. In conclusion, the studies on viral protein interaction maps suggest that cloned pathogen ORFeomes will contribute to a holistic picture of the pathogenesis of infectious diseases and are ideal starting points for new approaches ill systems biology. Both viral ORFeome and interaction mapping projects are being documented oil our Web site (http:/ /itgnivl.fzk.de/www/itg/uetz/virus/).
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