Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.

The mammalian epidermis is a continually renewing structure that provides the interface between the organism and an innately hostile environment. The keratinocyte is its principal cell. Keratinocyte proteins form a physical epithelial barrier, protect against microbial damage, and prepare immune res...

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Main Authors: Jennifer M Taylor, Teresa L Street, Lizhong Hao, Richard Copley, Martin S Taylor, Patrick J Hayden, Gina Stolper, Richard Mott, Jotun Hein, Miriam F Moffatt, William O C M Cookson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-10-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2766255?pdf=render
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spelling doaj-63ed74ac5e0e433a98ec98ab33d60b4d2020-11-25T02:05:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-10-01410e765110.1371/journal.pone.0007651Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.Jennifer M TaylorTeresa L StreetLizhong HaoRichard CopleyMartin S TaylorPatrick J HaydenGina StolperRichard MottJotun HeinMiriam F MoffattWilliam O C M CooksonThe mammalian epidermis is a continually renewing structure that provides the interface between the organism and an innately hostile environment. The keratinocyte is its principal cell. Keratinocyte proteins form a physical epithelial barrier, protect against microbial damage, and prepare immune responses to danger. Epithelial immunity is disordered in many common diseases and disordered epithelial differentiation underlies many cancers. In order to identify the genes that mediate epithelial development we used a tissue model of the skin derived from primary human keratinocytes. We measured global gene expression in triplicate at five times over the ten days that the keratinocytes took to fully differentiate. We identified 1282 gene transcripts that significantly changed during differentiation (false discovery rate <0.01%). We robustly grouped these transcripts by K-means clustering into modules with distinct temporal expression patterns, shared regulatory motifs, and biological functions. We found a striking cluster of late expressed genes that form the structural and innate immune defences of the epithelial barrier. Gene Ontology analyses showed that undifferentiated keratinocytes were characterised by genes for motility and the adaptive immune response. We systematically identified calcium-binding genes, which may operate with the epidermal calcium gradient to control keratinocyte division during skin repair. The results provide multiple novel insights into keratinocyte biology, in particular providing a comprehensive list of known and previously unrecognised major components of the epidermal barrier. The findings provide a reference for subsequent understanding of how the barrier functions in health and disease.http://europepmc.org/articles/PMC2766255?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jennifer M Taylor
Teresa L Street
Lizhong Hao
Richard Copley
Martin S Taylor
Patrick J Hayden
Gina Stolper
Richard Mott
Jotun Hein
Miriam F Moffatt
William O C M Cookson
spellingShingle Jennifer M Taylor
Teresa L Street
Lizhong Hao
Richard Copley
Martin S Taylor
Patrick J Hayden
Gina Stolper
Richard Mott
Jotun Hein
Miriam F Moffatt
William O C M Cookson
Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
PLoS ONE
author_facet Jennifer M Taylor
Teresa L Street
Lizhong Hao
Richard Copley
Martin S Taylor
Patrick J Hayden
Gina Stolper
Richard Mott
Jotun Hein
Miriam F Moffatt
William O C M Cookson
author_sort Jennifer M Taylor
title Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
title_short Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
title_full Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
title_fullStr Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
title_full_unstemmed Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
title_sort dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-10-01
description The mammalian epidermis is a continually renewing structure that provides the interface between the organism and an innately hostile environment. The keratinocyte is its principal cell. Keratinocyte proteins form a physical epithelial barrier, protect against microbial damage, and prepare immune responses to danger. Epithelial immunity is disordered in many common diseases and disordered epithelial differentiation underlies many cancers. In order to identify the genes that mediate epithelial development we used a tissue model of the skin derived from primary human keratinocytes. We measured global gene expression in triplicate at five times over the ten days that the keratinocytes took to fully differentiate. We identified 1282 gene transcripts that significantly changed during differentiation (false discovery rate <0.01%). We robustly grouped these transcripts by K-means clustering into modules with distinct temporal expression patterns, shared regulatory motifs, and biological functions. We found a striking cluster of late expressed genes that form the structural and innate immune defences of the epithelial barrier. Gene Ontology analyses showed that undifferentiated keratinocytes were characterised by genes for motility and the adaptive immune response. We systematically identified calcium-binding genes, which may operate with the epidermal calcium gradient to control keratinocyte division during skin repair. The results provide multiple novel insights into keratinocyte biology, in particular providing a comprehensive list of known and previously unrecognised major components of the epidermal barrier. The findings provide a reference for subsequent understanding of how the barrier functions in health and disease.
url http://europepmc.org/articles/PMC2766255?pdf=render
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