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Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions

The Crk adaptor family of proteins comprises the alternatively spliced CrkI and CrkII isoforms, as well as the paralog Crk-like (CrkL) protein, which is encoded by a different gene. Initially thought to be involved in signaling during apoptosis and cell adhesion, this ubiquitously expressed family o...

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Autores principales: Martinez-Quiles, Narcisa, Feuerbacher, Leigh Ann, Benito-León, María, Hardwidge, Philip R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260429/
https://www.ncbi.nlm.nih.gov/pubmed/25506591
http://dx.doi.org/10.1155/2014/372901
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author Martinez-Quiles, Narcisa
Feuerbacher, Leigh Ann
Benito-León, María
Hardwidge, Philip R.
author_facet Martinez-Quiles, Narcisa
Feuerbacher, Leigh Ann
Benito-León, María
Hardwidge, Philip R.
author_sort Martinez-Quiles, Narcisa
collection PubMed
description The Crk adaptor family of proteins comprises the alternatively spliced CrkI and CrkII isoforms, as well as the paralog Crk-like (CrkL) protein, which is encoded by a different gene. Initially thought to be involved in signaling during apoptosis and cell adhesion, this ubiquitously expressed family of proteins is now known to play essential roles in integrating signals from a wide range of stimuli. In this review, we describe the structure and function of the different Crk proteins. We then focus on the emerging roles of Crk adaptors during Enterobacteriaceae pathogenesis, with special emphasis on the important human pathogens Salmonella, Shigella, Yersinia, and enteropathogenic Escherichia coli. Throughout, we remark on opportunities for future research into this intriguing family of proteins.
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spelling pubmed-42604292014-12-14 Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions Martinez-Quiles, Narcisa Feuerbacher, Leigh Ann Benito-León, María Hardwidge, Philip R. Biomed Res Int Review Article The Crk adaptor family of proteins comprises the alternatively spliced CrkI and CrkII isoforms, as well as the paralog Crk-like (CrkL) protein, which is encoded by a different gene. Initially thought to be involved in signaling during apoptosis and cell adhesion, this ubiquitously expressed family of proteins is now known to play essential roles in integrating signals from a wide range of stimuli. In this review, we describe the structure and function of the different Crk proteins. We then focus on the emerging roles of Crk adaptors during Enterobacteriaceae pathogenesis, with special emphasis on the important human pathogens Salmonella, Shigella, Yersinia, and enteropathogenic Escherichia coli. Throughout, we remark on opportunities for future research into this intriguing family of proteins. Hindawi Publishing Corporation 2014 2014-11-25 /pmc/articles/PMC4260429/ /pubmed/25506591 http://dx.doi.org/10.1155/2014/372901 Text en Copyright © 2014 Narcisa Martinez-Quiles et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Martinez-Quiles, Narcisa
Feuerbacher, Leigh Ann
Benito-León, María
Hardwidge, Philip R.
Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title_full Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title_fullStr Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title_full_unstemmed Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title_short Contribution of Crk Adaptor Proteins to Host Cell and Bacteria Interactions
title_sort contribution of crk adaptor proteins to host cell and bacteria interactions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260429/
https://www.ncbi.nlm.nih.gov/pubmed/25506591
http://dx.doi.org/10.1155/2014/372901
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