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When Poly(A) Binding Proteins Meet Viral Infections, Including SARS-CoV-2.
Gao, Jie; Tang, Yan-Dong; Hu, Wei; Zheng, Chunfu.
  • Gao J; The State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia Universitygrid.411643.5, Hohhot, China.
  • Tang YD; State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Harbin, China.
  • Hu W; The State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia Universitygrid.411643.5, Hohhot, China.
  • Zheng C; State Key Laboratory of Genetic Engineering, Ministry of Education Key Laboratory of Contemporary Anthropology, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, China.
J Virol ; 96(7): e0013622, 2022 04 13.
Article in English | MEDLINE | ID: covidwho-1745828
ABSTRACT
Viruses have evolved diverse strategies to hijack the cellular gene expression system for their replication. The poly(A) binding proteins (PABPs), a family of critical gene expression factors, are viruses' common targets. PABPs act not only as a translation factor but also as a key factor of mRNA metabolism. During viral infections, the activities of PABPs are manipulated by various viruses, subverting the host translation machinery or evading the cellular antiviral defense mechanism. Viruses harness PABPs by modifying their stability, complex formation with other translation initiation factors, or subcellular localization to promote viral mRNAs translation while shutting off or competing with host protein synthesis. For the past decade, many studies have demonstrated the PABPs' roles during viral infection. This review summarizes a comprehensive perspective of PABPs' roles during viral infection and how viruses evade host antiviral defense through the manipulations of PABPs.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immune Evasion / Host Microbial Interactions / SARS-CoV-2 / COVID-19 Limits: Humans Language: English Journal: J Virol Year: 2022 Document Type: Article Affiliation country: Jvi.00136-22

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immune Evasion / Host Microbial Interactions / SARS-CoV-2 / COVID-19 Limits: Humans Language: English Journal: J Virol Year: 2022 Document Type: Article Affiliation country: Jvi.00136-22