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

Journal of cell science (2013-04-18)
Wu Zhou, Jean Paul Thiery
RESUMEN

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.

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Sigma-Aldrich
Anti-GIT2 antibody produced in rabbit, affinity isolated antibody
Sigma-Aldrich
Monoclonal Anti-SNAI2 antibody produced in mouse, clone 3C12, purified immunoglobulin, buffered aqueous solution