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CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors

Fam49 proteins, now referred to as CYRI (CYFIP-related Rac Interactor), are evolutionarily conserved across many phyla. Their closest relative by amino acid sequence is CYFIP, as both proteins contain a domain of unknown function DUF1394. We recently showed that CYRI and the DUF1394 can mediate bind...

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Autores principales: Whitelaw, Jamie A., Lilla, Sergio, Paul, Nikki R., Fort, Loic, Zanivan, Sara, Machesky, Laura M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682259/
https://www.ncbi.nlm.nih.gov/pubmed/31413787
http://dx.doi.org/10.1080/19420889.2019.1643665
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author Whitelaw, Jamie A.
Lilla, Sergio
Paul, Nikki R.
Fort, Loic
Zanivan, Sara
Machesky, Laura M.
author_facet Whitelaw, Jamie A.
Lilla, Sergio
Paul, Nikki R.
Fort, Loic
Zanivan, Sara
Machesky, Laura M.
author_sort Whitelaw, Jamie A.
collection PubMed
description Fam49 proteins, now referred to as CYRI (CYFIP-related Rac Interactor), are evolutionarily conserved across many phyla. Their closest relative by amino acid sequence is CYFIP, as both proteins contain a domain of unknown function DUF1394. We recently showed that CYRI and the DUF1394 can mediate binding to Rac1 and evidence is building to suggest that CYRI plays important roles in cell migration, chemotaxis and pathogen entry into cells. Here we discuss how CYRI proteins fit into the current framework of the control of actin dynamics by positive and negative feedback loops containing Rac1, the Scar/WAVE Complex, the Arp2/3 Complex and branched actin. We also provide data regarding the interaction between Rac1 and CYRI in an unbiassed mass spectrometry screen for interactors of an active mutant of Rac1.
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spelling pubmed-66822592019-08-14 CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors Whitelaw, Jamie A. Lilla, Sergio Paul, Nikki R. Fort, Loic Zanivan, Sara Machesky, Laura M. Commun Integr Biol Commentary Fam49 proteins, now referred to as CYRI (CYFIP-related Rac Interactor), are evolutionarily conserved across many phyla. Their closest relative by amino acid sequence is CYFIP, as both proteins contain a domain of unknown function DUF1394. We recently showed that CYRI and the DUF1394 can mediate binding to Rac1 and evidence is building to suggest that CYRI plays important roles in cell migration, chemotaxis and pathogen entry into cells. Here we discuss how CYRI proteins fit into the current framework of the control of actin dynamics by positive and negative feedback loops containing Rac1, the Scar/WAVE Complex, the Arp2/3 Complex and branched actin. We also provide data regarding the interaction between Rac1 and CYRI in an unbiassed mass spectrometry screen for interactors of an active mutant of Rac1. Taylor & Francis 2019-07-23 /pmc/articles/PMC6682259/ /pubmed/31413787 http://dx.doi.org/10.1080/19420889.2019.1643665 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Whitelaw, Jamie A.
Lilla, Sergio
Paul, Nikki R.
Fort, Loic
Zanivan, Sara
Machesky, Laura M.
CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title_full CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title_fullStr CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title_full_unstemmed CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title_short CYRI/ Fam49 Proteins Represent a New Class of Rac1 Interactors
title_sort cyri/ fam49 proteins represent a new class of rac1 interactors
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682259/
https://www.ncbi.nlm.nih.gov/pubmed/31413787
http://dx.doi.org/10.1080/19420889.2019.1643665
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