4.7 Article

An Intrinsically Disordered Region of the DNA Repair Protein Nbs1 Is a Species-Specific Barrier to Herpes Simplex Virus 1 in Primates

Journal

CELL HOST & MICROBE
Volume 20, Issue 2, Pages 178-188

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2016.07.003

Keywords

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Funding

  1. National Institutes of Health [R01-GM-093086, R01-NS-082240]
  2. Investigator in the Pathogenesis of Infectious Disease award from the Burroughs Wellcome Fund
  3. NIH F30 award [F30 CA171715]
  4. NIH T32 award [T32 NS007180]

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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.

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