Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family

<p>Abstract</p> <p>Background</p> <p>Tight junctions are an intercellular adhesion complex of epithelial and endothelial cells, and form a paracellular barrier that restricts the diffusion of solutes on the basis of size and charge. Tight junctions are formed by multipr...

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Main Authors: Balda Maria S, Rodrigues Nelio TL, Steed Emily, Matter Karl
Format: Article
Language:English
Published: BMC 2009-12-01
Series:BMC Cell Biology
Online Access:http://www.biomedcentral.com/1471-2121/10/95
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spelling doaj-fe2016e4426b4760a68a61db738686692020-11-25T00:23:26ZengBMCBMC Cell Biology1471-21212009-12-011019510.1186/1471-2121-10-95Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin familyBalda Maria SRodrigues Nelio TLSteed EmilyMatter Karl<p>Abstract</p> <p>Background</p> <p>Tight junctions are an intercellular adhesion complex of epithelial and endothelial cells, and form a paracellular barrier that restricts the diffusion of solutes on the basis of size and charge. Tight junctions are formed by multiprotein complexes containing cytosolic and transmembrane proteins. How these components work together to form functional tight junctions is still not well understood and will require a complete understanding of the molecular composition of the junction.</p> <p>Results</p> <p>Here we identify a new transmembrane component of tight junctions: MarvelD3, a four-span transmembrane protein. Its predicted transmembrane helices form a Marvel (MAL and related proteins for vesicle traffic and membrane link) domain, a structural motif originally discovered in proteins involved in membrane apposition and fusion events, such as the tight junction proteins occludin and tricellulin. In mammals, MarvelD3 is expressed as two alternatively spliced isoforms. Both isoforms exhibit a broad tissue distribution and are expressed by different types of epithelial as well as endothelial cells. MarvelD3 co-localises with occludin at tight junctions in intestinal and corneal epithelial cells. RNA interference experiments in Caco-2 cells indicate that normal MarvelD3 expression is not required for the formation of functional tight junctions but depletion results in monolayers with increased transepithelial electrical resistance.</p> <p>Conclusions</p> <p>Our data indicate that MarvelD3 is a third member of the tight junction-associated occludin family of transmembrane proteins. Similar to occludin, normal expression of MarvelD3 is not essential for the formation of functional tight junctions. However, MarvelD3 functions as a determinant of epithelial paracellular permeability properties.</p> http://www.biomedcentral.com/1471-2121/10/95
collection DOAJ
language English
format Article
sources DOAJ
author Balda Maria S
Rodrigues Nelio TL
Steed Emily
Matter Karl
spellingShingle Balda Maria S
Rodrigues Nelio TL
Steed Emily
Matter Karl
Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
BMC Cell Biology
author_facet Balda Maria S
Rodrigues Nelio TL
Steed Emily
Matter Karl
author_sort Balda Maria S
title Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
title_short Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
title_full Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
title_fullStr Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
title_full_unstemmed Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family
title_sort identification of marveld3 as a tight junction-associated transmembrane protein of the occludin family
publisher BMC
series BMC Cell Biology
issn 1471-2121
publishDate 2009-12-01
description <p>Abstract</p> <p>Background</p> <p>Tight junctions are an intercellular adhesion complex of epithelial and endothelial cells, and form a paracellular barrier that restricts the diffusion of solutes on the basis of size and charge. Tight junctions are formed by multiprotein complexes containing cytosolic and transmembrane proteins. How these components work together to form functional tight junctions is still not well understood and will require a complete understanding of the molecular composition of the junction.</p> <p>Results</p> <p>Here we identify a new transmembrane component of tight junctions: MarvelD3, a four-span transmembrane protein. Its predicted transmembrane helices form a Marvel (MAL and related proteins for vesicle traffic and membrane link) domain, a structural motif originally discovered in proteins involved in membrane apposition and fusion events, such as the tight junction proteins occludin and tricellulin. In mammals, MarvelD3 is expressed as two alternatively spliced isoforms. Both isoforms exhibit a broad tissue distribution and are expressed by different types of epithelial as well as endothelial cells. MarvelD3 co-localises with occludin at tight junctions in intestinal and corneal epithelial cells. RNA interference experiments in Caco-2 cells indicate that normal MarvelD3 expression is not required for the formation of functional tight junctions but depletion results in monolayers with increased transepithelial electrical resistance.</p> <p>Conclusions</p> <p>Our data indicate that MarvelD3 is a third member of the tight junction-associated occludin family of transmembrane proteins. Similar to occludin, normal expression of MarvelD3 is not essential for the formation of functional tight junctions. However, MarvelD3 functions as a determinant of epithelial paracellular permeability properties.</p>
url http://www.biomedcentral.com/1471-2121/10/95
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