| Literature DB >> 27512903 |
Dianne I Lou1, Eui Tae Kim2, Nicholas R Meyerson3, Neha J Pancholi4, Kareem N Mohni5, David Enard6, Dmitri A Petrov6, Sandra K Weller5, Matthew D Weitzman7, Sara L Sawyer8.
Abstract
Humans occasionally transmit herpes simplex virus 1 (HSV-1) to captive primates, who reciprocally harbor alphaherpesviruses poised for zoonotic transmission to humans. To understand the basis for the species-specific restriction of HSV-1 in primates, we simulated what might happen during the cross-species transmission of HSV-1 and found that the DNA repair protein Nbs1 from only some primate species is able to promote HSV-1 infection. The Nbs1 homologs that promote HSV-1 infection also interact with the HSV-1 ICP0 protein. ICP0 interaction mapped to a region of structural disorder in the Nbs1 protein. Chimeras reversing patterns of disorder in Nbs1 reversed titers of HSV-1 produced in the cell. By extending this analysis to 1,237 virus-interacting mammalian proteins, we show that proteins that interact with viruses are highly enriched in disorder, suggesting that viruses commonly interact with host proteins through intrinsically disordered domains.Entities:
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Year: 2016 PMID: 27512903 PMCID: PMC4982468 DOI: 10.1016/j.chom.2016.07.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023