DUB3 Deubiquitylating Enzymes Regulate Hippo Pathway Activity by Regulating the Stability of ITCH, LATS and AMOT Proteins

Research output: Contribution to journalJournal articleResearchpeer-review

  • Thanh Hung Nguyen
  • Jan-Michael Kugler
  • Stephen Michael Cohen
The YAP and TAZ transcriptional coactivators promote oncogenic transformation. Elevated YAP/TAZ activity has been documented in human tumors. YAP and TAZ are negatively regulated by the Hippo tumor suppressor pathway. The activity and stability of several Hippo pathway components, including YAP/TAZ, is regulated by ubiquitin mediated protein turnover and several ubiquitin ligase complexes have been implicated in human cancer. However, little is known about the deubiquitylating enzymes that counteract these ubiquitin ligases in regulation of the Hippo pathway. Here we identify the DUB3 family deubiquitylating enzymes as regulators of Hippo pathway activity. We provide evidence that DUB3 proteins regulate YAP/TAZ activity by controlling the stability of the E3 ligase ITCH, the LATS kinases and the AMOT family proteins. As a novel Hippo pathway regulator, DUB3 has the potential to act a tumor suppressor by limiting YAP activity
Original languageEnglish
Article numbere0169587
JournalPLOS ONE
Volume12
Issue number1
Number of pages15
ISSN1932-6203
DOIs
Publication statusPublished - 6 Jan 2017

Number of downloads are based on statistics from Google Scholar and www.ku.dk


No data available

ID: 172137890