Post-transcriptional gene silencing activity of human GIGYF2

Biochem Biophys Res Commun. 2016 Jul 1;475(3):289-94. doi: 10.1016/j.bbrc.2016.05.022. Epub 2016 May 5.

Abstract

In mammalian post-transcriptional gene silencing, the Argonaute protein AGO2 indirectly recruits translation inhibitors, deadenylase complexes, and decapping factors to microRNA-targeted mRNAs, thereby repressing mRNA translation and accelerating mRNA decay. However, the exact composition and assembly pathway of the microRNA-induced silencing complex are not completely elucidated. As the GYF domain of human GIGYF2 was shown to bind AGO2 in pulldown experiments, we wondered whether GIGYF2 could be a novel protein component of the microRNA-induced silencing complex. Here we show that full-length GIGYF2 coimmunoprecipitates with AGO2 in human cells, and demonstrate that, upon tethering to a reporter mRNA, GIGYF2 exhibits strong, dose-dependent silencing activity, involving both mRNA destabilization and translational repression.

Keywords: Argonaute 2; GIGYF2; Post-transcriptional gene silencing; RNA-induced silencing complex; TNRC6.

MeSH terms

  • Argonaute Proteins / metabolism*
  • Carrier Proteins / metabolism*
  • Gene Silencing*
  • Genes, Reporter
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Protein Biosynthesis*
  • Protein Interaction Maps
  • RNA Stability
  • RNA, Messenger / chemistry
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism

Substances

  • AGO2 protein, human
  • Argonaute Proteins
  • Carrier Proteins
  • GIGYF2 protein, human
  • RNA, Messenger