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Tumor suppressor Interferon Regulatory Factor 1 selectively blocks expression of endogenous retrovirus.

K P Stoltz | C N Jondle | K Pulakanti | P A Sylvester | R Urrutia | S Rao | V L Tarakanova
Virology | 2019

Endogenous retroviruses (ERVs) comprise 10% of the genome, with many of these transcriptionally silenced post early embryogenesis. Several stimuli, including exogenous virus infection and cellular transformation can reactivate ERV expression via a poorly understood mechanism. We identified Interferon Regulatory Factor 1 (IRF-1), a tumor suppressor and an antiviral host factor, as a suppressor of ERV expression. IRF-1 decreased expression of a specific mouse ERV in vitro and in vivo. IRF-3, but not IRF-7, also decreased expression of distinct ERV families, suggesting that suppression of ERVs is a relevant biological function of the IRF family. Given the emerging appreciation of the physiological relevance of ERV expression in cancer, IRF-1-mediated suppression of specific ERVs may contribute to the overall tumor suppressor activity of this host factor.

Pubmed ID: 30342302

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA183593
  • Agency: NCI NIH HHS, United States
    Id: R01 CA203923
  • Agency: NCI NIH HHS, United States
    Id: R01 CA204231
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK052913

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