Cargando…

EPI64 regulates microvillar subdomains and structure

EPI64 is a TBC domain–containing protein that binds the PDZ domains of EBP50, which binds ezrin, a major actin-binding protein of microvilli. High-resolution light microscopy revealed that ezrin and EBP50 localize exclusively to the membrane-surrounded region of microvilli, whereas EPI64 localizes t...

Descripción completa

Detalles Bibliográficos
Autores principales: Hanono, Abraham, Garbett, Damien, Reczek, David, Chambers, David N., Bretscher, Anthony
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064679/
https://www.ncbi.nlm.nih.gov/pubmed/17145964
http://dx.doi.org/10.1083/jcb.200604046
_version_ 1782137593774735360
author Hanono, Abraham
Garbett, Damien
Reczek, David
Chambers, David N.
Bretscher, Anthony
author_facet Hanono, Abraham
Garbett, Damien
Reczek, David
Chambers, David N.
Bretscher, Anthony
author_sort Hanono, Abraham
collection PubMed
description EPI64 is a TBC domain–containing protein that binds the PDZ domains of EBP50, which binds ezrin, a major actin-binding protein of microvilli. High-resolution light microscopy revealed that ezrin and EBP50 localize exclusively to the membrane-surrounded region of microvilli, whereas EPI64 localizes to variable regions in the structures. Overexpressing EPI64 results in its and EBP50's relocalization to the base of microvilli, including to the actin rootlet devoid of ezrin or plasma membrane. Uncoupling EPI64's binding to EBP50, expression of any construct mislocalizing its TBC domain, or knock down of EBP50 results in loss of microvilli. The TBC domain of EPI64 binds directly to Arf6-GTP. Overexpressing the TBC domain increases Arf6-GTP levels, and expressing dominant-active Arf6 results in microvillar loss. These data reveal that microvilli have distinct cytoskeletal subdomains and that EPI64 regulates microvillar structure.
format Text
id pubmed-2064679
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-20646792007-11-29 EPI64 regulates microvillar subdomains and structure Hanono, Abraham Garbett, Damien Reczek, David Chambers, David N. Bretscher, Anthony J Cell Biol Research Articles EPI64 is a TBC domain–containing protein that binds the PDZ domains of EBP50, which binds ezrin, a major actin-binding protein of microvilli. High-resolution light microscopy revealed that ezrin and EBP50 localize exclusively to the membrane-surrounded region of microvilli, whereas EPI64 localizes to variable regions in the structures. Overexpressing EPI64 results in its and EBP50's relocalization to the base of microvilli, including to the actin rootlet devoid of ezrin or plasma membrane. Uncoupling EPI64's binding to EBP50, expression of any construct mislocalizing its TBC domain, or knock down of EBP50 results in loss of microvilli. The TBC domain of EPI64 binds directly to Arf6-GTP. Overexpressing the TBC domain increases Arf6-GTP levels, and expressing dominant-active Arf6 results in microvillar loss. These data reveal that microvilli have distinct cytoskeletal subdomains and that EPI64 regulates microvillar structure. The Rockefeller University Press 2006-12-04 /pmc/articles/PMC2064679/ /pubmed/17145964 http://dx.doi.org/10.1083/jcb.200604046 Text en Copyright © 2006, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Hanono, Abraham
Garbett, Damien
Reczek, David
Chambers, David N.
Bretscher, Anthony
EPI64 regulates microvillar subdomains and structure
title EPI64 regulates microvillar subdomains and structure
title_full EPI64 regulates microvillar subdomains and structure
title_fullStr EPI64 regulates microvillar subdomains and structure
title_full_unstemmed EPI64 regulates microvillar subdomains and structure
title_short EPI64 regulates microvillar subdomains and structure
title_sort epi64 regulates microvillar subdomains and structure
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064679/
https://www.ncbi.nlm.nih.gov/pubmed/17145964
http://dx.doi.org/10.1083/jcb.200604046
work_keys_str_mv AT hanonoabraham epi64regulatesmicrovillarsubdomainsandstructure
AT garbettdamien epi64regulatesmicrovillarsubdomainsandstructure
AT reczekdavid epi64regulatesmicrovillarsubdomainsandstructure
AT chambersdavidn epi64regulatesmicrovillarsubdomainsandstructure
AT bretscheranthony epi64regulatesmicrovillarsubdomainsandstructure