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Phosphorylation by cellular casein kinase II is essential for transcriptional activity of vesicular stomatitis virus phosphoprotein P.
Author(s) -
Sailen Barik,
A K Banerjee
Publication year - 1992
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.89.14.6570
Subject(s) - casein kinase 2 , protein kinase r , phosphoprotein , vesicular stomatitis virus , casein kinase 1 , biology , cyclin dependent kinase 9 , map2k7 , cyclin dependent kinase 2 , mitogen activated protein kinase kinase , protein kinase a , casein kinase 2, alpha 1 , kinase , biochemistry , c raf , microbiology and biotechnology , rhabdoviridae , phosphorylation , virus , virology
We have previously shown that phosphorylation of vesicular stomatitis virus (VSV) phosphoprotein P by cellular protein kinase activity is an essential prerequisite for its transcriptional function. We have now purified this protein kinase by monitoring its ability to phosphorylate bacterially expressed, unphosphorylated P protein. Biochemical studies showed that the kinase is indistinguishable from casein kinase II, a ubiquitous cyclic AMP-independent protein kinase present in a wide variety of eukaryotic cells and tissues. Functional VSV transcription could be reconstituted with viral L protein, N-RNA template, and P protein phosphorylated by either purified cellular protein kinase or purified casein kinase II. The unusual role of casein kinase II in the transcription process of a nonsegmented negative-strand RNA virus would have important implications in host-virus interactions and antiviral therapy.

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