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SARS-Cov-2 small viral RNA suppresses gene expression via complementary binding to mRNA 3' UTR.
Delcher, Haley A; DeMeis, Jeffrey D; Ghobar, Nicole; Godang, Noel L; Knight, Sierra L; Alqudah, Shahem Y; Nguyen, Kevin N; Watters, Brianna C; Borchert, Glen M.
Afiliação
  • Delcher HA; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • DeMeis JD; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Ghobar N; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Godang NL; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Knight SL; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Alqudah SY; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Nguyen KN; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Watters BC; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
  • Borchert GM; Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL.
MicroPubl Biol ; 20242024.
Article em En | MEDLINE | ID: mdl-38312351
ABSTRACT
SARS-CoV-2 (SC2) has been intensely studied since its emergence. However, the mechanisms of host immune dysregulation triggered by SC2 remain poorly understood. That said, it is well established that many prominent viral families encode microRNAs (miRNAs) or related small viral RNAs (svRNAs) capable of regulating human genes involved in immune function. Importantly, recent reports have shown that SC2 encodes its own svRNAs. In this study, we have identified 12 svRNAs expressed during SC2 infection and show that one of these svRNAs can regulate target gene expression via complementary binding to mRNA 3' untranslated regions (3'UTRs) much like human microRNAs.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article