| Literature DB >> 23591815 |
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.Entities:
Keywords: EMT; Git2; Zeb1; miR-146a
Mesh:
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Year: 2013 PMID: 23591815 DOI: 10.1242/jcs.126367
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285