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Journal of General Virology, Vol 78, 3327-3331, Copyright © 1997 by Society for General Microbiology
ARTICLES |
A Phelan and JB Clements
Institute of Virology, University of Glasgow, UK.
Herpes simplex virus type 1 (HSV-1) immediate early protein IE63, an essential nuclear protein, is pleiotropic in function and, at the post- transcriptional level, inhibits RNA splicing, interacts with cellular splicing small nuclear ribonucleoprotein particles (snRNPs), binds RNA and prevents the nucleocytoplasmic transport of intron-containing mRNAs. Here it is reported that IE63 is a nucleocytoplasmic shuttle protein able to travel from snRNP- and RNA-rich nuclear foci to the cytoplasm, where it accumulates during actinomycin D treatment. This newly identified property suggests that IE63 facilitates nuclear export of HSV-1 transcripts, in addition to retaining intron-containing transcripts in the nucleus. The mechanism by which IE63 controls RNA export has yet to be defined.
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Y. Zhi and R. M. Sandri-Goldin Analysis of the Phosphorylation Sites of Herpes Simplex Virus Type 1 Regulatory Protein ICP27 J. Virol., April 1, 1999; 73(4): 3246 - 3257. [Abstract] [Full Text] |
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