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From APOBEC to ZAP: Diverse mechanisms used by cellular restriction factors to inhibit virus infections.
Chemudupati, Mahesh; Kenney, Adam D; Bonifati, Serena; Zani, Ashley; McMichael, Temet M; Wu, Li; Yount, Jacob S.
Afiliação
  • Chemudupati M; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • Kenney AD; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • Bonifati S; Department of Veterinary Biosciences, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • Zani A; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • McMichael TM; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • Wu L; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Department of Veterinary Biosciences, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
  • Yount JS; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA. Electronic address: yount.37@osu.edu.
Biochim Biophys Acta Mol Cell Res ; 1866(3): 382-394, 2019 03.
Article em En | MEDLINE | ID: mdl-30290238
ABSTRACT
Antiviral restriction factors are cellular proteins that inhibit the entry, replication, or spread of viruses. These proteins are critical components of the innate immune system and function to limit the severity and host range of virus infections. Here we review the current knowledge on the mechanisms of action of several restriction factors that affect multiple viruses at distinct stages of their life cycles. For example, APOBEC3G deaminates cytosines to hypermutate reverse transcribed viral DNA; IFITM3 alters membranes to inhibit virus membrane fusion; MXA/B oligomerize on viral protein complexes to inhibit virus replication; SAMHD1 decreases dNTP intracellular concentrations to prevent reverse transcription of retrovirus genomes; tetherin prevents release of budding virions from cells; Viperin catalyzes formation of a nucleoside analogue that inhibits viral RNA polymerases; and ZAP binds virus RNAs to target them for degradation. We also discuss countermeasures employed by specific viruses against these restriction factors, and mention secondary functions of several of these factors in modulating immune responses. These important examples highlight the diverse strategies cells have evolved to combat virus infections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Viroses / Proteínas Nucleares / Fosfotransferases (Aceptor do Grupo Álcool) / Desaminases APOBEC Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Viroses / Proteínas Nucleares / Fosfotransferases (Aceptor do Grupo Álcool) / Desaminases APOBEC Idioma: En Ano de publicação: 2019 Tipo de documento: Article