Loss of Git2 induces epithelial-mesenchymal transition by miR146a-Cnot6L-controlled expression of Zeb1

J Cell Sci. 2013 Jun 15;126(Pt 12):2740-6. doi: 10.1242/jcs.126367. Epub 2013 Apr 16.

Abstract

Epithelial-mesenchymal transition (EMT) can be induced by several pleiotropically activated transcription factors, including the zinc-finger E-box-binding protein Zeb1. Mechanisms regulating Zeb1 expression have been partly uncovered, showing a critical role for the miR-200 family members. In the present study, we show that Zeb1 is regulated by the Arf GTPase-activating protein (GAP) Git2. Following the loss of Git2, we found that miR-146a maturation is enhanced, which in turn promotes the expression of Zeb1 and induction of EMT. Furthermore, we found that Cnot6L, a validated target of miR-146a, affects the stability of Zeb1 mRNA through its deadenylase activity. Our results present evidence for a new role for loss of Git2 in promoting EMT through a novel regulatory pathway.

Keywords: EMT; Git2; Zeb1; miR-146a.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Epithelial Cells / metabolism
  • Epithelial-Mesenchymal Transition / genetics*
  • GTPase-Activating Proteins / genetics*
  • GTPase-Activating Proteins / metabolism
  • Gene Expression
  • Hep G2 Cells
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • RNA, Messenger / genetics
  • Ribonucleases / genetics*
  • Ribonucleases / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Zinc Finger E-box-Binding Homeobox 1

Substances

  • GIT2 protein, human
  • GTPase-Activating Proteins
  • Homeodomain Proteins
  • MicroRNAs
  • RNA, Messenger
  • Transcription Factors
  • ZEB1 protein, human
  • Zinc Finger E-box-Binding Homeobox 1
  • CNOT6L protein, human
  • Ribonucleases