SGEF forms a complex with Scribble and Dlg1 and regulates epithelial junctions and contractility

Author:

Awadia Sahezeel1ORCID,Huq Farah2,Arnold Torey R.2,Goicoechea Silvia M.1,Sun Young Joo3ORCID,Hou Titus3ORCID,Kreider-Letterman Gabriel1ORCID,Massimi Paola4,Banks Lawrence4,Fuentes Ernesto J.3ORCID,Miller Ann L.2ORCID,Garcia-Mata Rafael1ORCID

Affiliation:

1. Department of Biological Sciences, The University of Toledo, Toledo, OH

2. Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI

3. Department of Biochemistry, University of Iowa, Iowa City, IA

4. International Center for Genetic Engineering and Biotechnology, Trieste, Italy

Abstract

The canonical Scribble polarity complex is implicated in regulation of epithelial junctions and apical polarity. Here, we show that SGEF, a RhoG-specific GEF, forms a ternary complex with Scribble and Dlg1, two members of the Scribble complex. SGEF targets to apical junctions in a Scribble-dependent fashion and functions in the regulation of actomyosin-based contractility and barrier function at tight junctions as well as E-cadherin–mediated formation of adherens junctions. Surprisingly, SGEF does not control the establishment of polarity. However, in 3D cysts, SGEF regulates the formation of a single open lumen. Interestingly, SGEF’s nucleotide exchange activity regulates the formation and maintenance of adherens junctions, and in cysts the number of lumens formed, whereas SGEF’s scaffolding activity is critical for regulation of actomyosin contractility and lumen opening. We propose that SGEF plays a key role in coordinating junctional assembly and actomyosin contractility by bringing together Scribble and Dlg1 and targeting RhoG activation to cell–cell junctions.

Funder

US Department of Energy

National Institutes of Health

National Science Foundation

American Heart Association

Associazione Italiana per la Ricerca sul Cancro

Publisher

Rockefeller University Press

Subject

Cell Biology

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