Cargando…

Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition

The merlin-ERM (ezrin, radixin, moesin) family of proteins plays a central role in linking the cellular membranes to the cortical actin cytoskeleton. Merlin regulates contact inhibition and is an integral part of cell–cell junctions, while ERM proteins, ezrin, radixin and moesin, assist in the forma...

Descripción completa

Detalles Bibliográficos
Autores principales: Michie, Katharine A., Bermeister, Adam, Robertson, Neil O., Goodchild, Sophia C., Curmi, Paul M. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515277/
https://www.ncbi.nlm.nih.gov/pubmed/31018575
http://dx.doi.org/10.3390/ijms20081996
_version_ 1783418054633324544
author Michie, Katharine A.
Bermeister, Adam
Robertson, Neil O.
Goodchild, Sophia C.
Curmi, Paul M. G.
author_facet Michie, Katharine A.
Bermeister, Adam
Robertson, Neil O.
Goodchild, Sophia C.
Curmi, Paul M. G.
author_sort Michie, Katharine A.
collection PubMed
description The merlin-ERM (ezrin, radixin, moesin) family of proteins plays a central role in linking the cellular membranes to the cortical actin cytoskeleton. Merlin regulates contact inhibition and is an integral part of cell–cell junctions, while ERM proteins, ezrin, radixin and moesin, assist in the formation and maintenance of specialized plasma membrane structures and membrane vesicle structures. These two protein families share a common evolutionary history, having arisen and separated via gene duplication near the origin of metazoa. During approximately 0.5 billion years of evolution, the merlin and ERM family proteins have maintained both sequence and structural conservation to an extraordinary level. Comparing crystal structures of merlin-ERM proteins and their complexes, a picture emerges of the merlin-ERM proteins acting as switchable interaction hubs, assembling protein complexes on cellular membranes and linking them to the actin cytoskeleton. Given the high level of structural conservation between the merlin and ERM family proteins we speculate that they may function together.
format Online
Article
Text
id pubmed-6515277
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-65152772019-05-30 Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition Michie, Katharine A. Bermeister, Adam Robertson, Neil O. Goodchild, Sophia C. Curmi, Paul M. G. Int J Mol Sci Review The merlin-ERM (ezrin, radixin, moesin) family of proteins plays a central role in linking the cellular membranes to the cortical actin cytoskeleton. Merlin regulates contact inhibition and is an integral part of cell–cell junctions, while ERM proteins, ezrin, radixin and moesin, assist in the formation and maintenance of specialized plasma membrane structures and membrane vesicle structures. These two protein families share a common evolutionary history, having arisen and separated via gene duplication near the origin of metazoa. During approximately 0.5 billion years of evolution, the merlin and ERM family proteins have maintained both sequence and structural conservation to an extraordinary level. Comparing crystal structures of merlin-ERM proteins and their complexes, a picture emerges of the merlin-ERM proteins acting as switchable interaction hubs, assembling protein complexes on cellular membranes and linking them to the actin cytoskeleton. Given the high level of structural conservation between the merlin and ERM family proteins we speculate that they may function together. MDPI 2019-04-23 /pmc/articles/PMC6515277/ /pubmed/31018575 http://dx.doi.org/10.3390/ijms20081996 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Michie, Katharine A.
Bermeister, Adam
Robertson, Neil O.
Goodchild, Sophia C.
Curmi, Paul M. G.
Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title_full Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title_fullStr Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title_full_unstemmed Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title_short Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
title_sort two sides of the coin: ezrin/radixin/moesin and merlin control membrane structure and contact inhibition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515277/
https://www.ncbi.nlm.nih.gov/pubmed/31018575
http://dx.doi.org/10.3390/ijms20081996
work_keys_str_mv AT michiekatharinea twosidesofthecoinezrinradixinmoesinandmerlincontrolmembranestructureandcontactinhibition
AT bermeisteradam twosidesofthecoinezrinradixinmoesinandmerlincontrolmembranestructureandcontactinhibition
AT robertsonneilo twosidesofthecoinezrinradixinmoesinandmerlincontrolmembranestructureandcontactinhibition
AT goodchildsophiac twosidesofthecoinezrinradixinmoesinandmerlincontrolmembranestructureandcontactinhibition
AT curmipaulmg twosidesofthecoinezrinradixinmoesinandmerlincontrolmembranestructureandcontactinhibition