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肿瘤抑制因子干扰素调节因子 1 选择性地阻断内源性逆转录病毒的表达。

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

机构信息

Microbiology and Immunology Department, Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Blood Research Institute, BloodCenter of Wisconsin, a Part of Versiti, 8727 West Watertown Plank Road, Milwaukee, WI 53226, United States.

出版信息

Virology. 2019 Jan 2;526:52-60. doi: 10.1016/j.virol.2018.10.003. Epub 2018 Oct 17.

Abstract

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.

摘要

内源性逆转录病毒 (ERV) 占基因组的 10%,其中许多在早期胚胎发生后转录沉默。多种刺激因素,包括外源病毒感染和细胞转化,可以通过一种尚未完全了解的机制重新激活 ERV 的表达。我们发现干扰素调节因子 1(IRF-1)作为一种肿瘤抑制因子和抗病毒宿主因子,可抑制 ERV 的表达。IRF-1 在体外和体内降低了特定的小鼠 ERV 的表达。IRF-3,但不是 IRF-7,也降低了不同 ERV 家族的表达,这表明抑制 ERV 是 IRF 家族的一个相关生物学功能。鉴于 ERV 表达在癌症中的生理相关性日益受到重视,IRF-1 介导的特定 ERV 的抑制可能有助于该宿主因子的整体肿瘤抑制活性。

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