Expanded directly binds conserved regions of Fat to restrain growth via the Hippo pathway

Author:

Fulford Alexander D.1ORCID,Enderle Leonie2ORCID,Rusch Jannette1ORCID,Hodzic Didier1ORCID,Holder Maxine V.3ORCID,Earl Alex1ORCID,Oh Robin Hyunseo2ORCID,Tapon Nicolas3ORCID,McNeill Helen12ORCID

Affiliation:

1. Washington University School of Medicine 1 Department of Developmental Biology, , St. Louis, USA

2. University of Toronto 2 Department of Molecular Genetics, , Toronto, Canada

3. Apoptosis and Proliferation Control Laboratory, The Francis Crick Institute 3 , London, UK

Abstract

The Hippo pathway is a conserved and critical regulator of tissue growth. The FERM protein Expanded is a key signaling hub that promotes activation of the Hippo pathway, thereby inhibiting the transcriptional co-activator Yorkie. Previous work identified the polarity determinant Crumbs as a primary regulator of Expanded. Here, we show that the giant cadherin Fat also regulates Expanded directly and independently of Crumbs. We show that direct binding between Expanded and a highly conserved region of the Fat cytoplasmic domain recruits Expanded to the apicolateral junctional zone and stabilizes Expanded. In vivo deletion of Expanded binding regions in Fat causes loss of apical Expanded and promotes tissue overgrowth. Unexpectedly, we find Fat can bind its ligand Dachsous via interactions of their cytoplasmic domains, in addition to the known extracellular interactions. Importantly, Expanded is stabilized by Fat independently of Dachsous binding. These data provide new mechanistic insights into how Fat regulates Expanded, and how Hippo signaling is regulated during organ growth.

Funder

National Institutes of Health

BJC

Francis Crick Institute

Cancer Research UK

UK Medical Research Council

Wellcome Trust

Publisher

Rockefeller University Press

Subject

Cell Biology

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