Scrib module proteins: Control of epithelial architecture and planar spindle orientation.

Int J Biochem Cell Biol

Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai, Japan; Graduate School of Life Sciences, Tohoku University, Sendai, Japan. Electronic address:

Published: July 2021

AI Article Synopsis

  • Scrib module proteins (Scrib, Dlg, Lgl) are key regulators of cell polarity, initially identified as tumor suppressors in fruit flies and linked to cancer in mammals.
  • Recent research highlights their role in maintaining epithelial architecture, influencing aspects like cell polarity, junction formation, and spindle orientation during division.
  • This review emphasizes the molecular functions of Scrib module proteins and their significance in epithelial organization, based on recent in vivo studies.

Article Abstract

The Scrib module proteins, Scrib, Dlg, and Lgl, are conserved regulators of cell polarity in diverse biological contexts. Originally discovered as neoplastic tumor suppressors in the fruit fly Drosophila melanogaster, disruption of Scrib module components leads to tumorigenesis in mammalian epithelia and is associated with human cancers. With multiple protein interacting domains, Scrib module proteins function as determinants of basolateral identity in epithelial cells with apical-basal polarity while acting as signaling platform scaffold proteins. Recent studies have further revealed novel roles of the Scrib module in the control of epithelial architecture, ranging from polarity establishment and tricellular junction formation to planar spindle orientation during cell division. This review updates the current understanding of the molecular nature and physiological functions of the Scrib module with a focus on in vivo studies, providing a framework for how these protein dynamics affect the processes of epithelial organization.

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Source
http://dx.doi.org/10.1016/j.biocel.2021.106001DOI Listing

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