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Tissue-specific regulatory elements in mammalian promoters

Transcription factor-binding sites and the cis-regulatory modules they compose are central determinants of gene expression. We previously showed that binding site motifs and modules in proximal promoters can be used to predict a significant portion of mammalian tissue-specific transcription. Here, w...

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Detalles Bibliográficos
Autores principales: Smith, Andrew D, Sumazin, Pavel, Zhang, Michael Q
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800356/
https://www.ncbi.nlm.nih.gov/pubmed/17224917
http://dx.doi.org/10.1038/msb4100114
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author Smith, Andrew D
Sumazin, Pavel
Zhang, Michael Q
author_facet Smith, Andrew D
Sumazin, Pavel
Zhang, Michael Q
author_sort Smith, Andrew D
collection PubMed
description Transcription factor-binding sites and the cis-regulatory modules they compose are central determinants of gene expression. We previously showed that binding site motifs and modules in proximal promoters can be used to predict a significant portion of mammalian tissue-specific transcription. Here, we report on a systematic analysis of promoters controlling tissue-specific expression in heart, kidney, liver, pancreas, skeletal muscle, testis and CD4 T cells, for both human and mouse. We integrated multiple sources of expression data to compile sets of transcripts with strong evidence for tissue-specific regulation. The analysis of the promoters corresponding to these sets produced a catalog of predicted tissue-specific motifs and modules, and cis-regulatory elements. Predicted regulatory interactions are supported by statistical evidence, and provide a foundation for targeted experiments that will improve our understanding of tissue-specific regulatory networks. In a broader context, methods used to construct the catalog provide a model for the analysis of genomic regions that regulate differentially expressed genes.
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spelling pubmed-18003562007-03-26 Tissue-specific regulatory elements in mammalian promoters Smith, Andrew D Sumazin, Pavel Zhang, Michael Q Mol Syst Biol Report Transcription factor-binding sites and the cis-regulatory modules they compose are central determinants of gene expression. We previously showed that binding site motifs and modules in proximal promoters can be used to predict a significant portion of mammalian tissue-specific transcription. Here, we report on a systematic analysis of promoters controlling tissue-specific expression in heart, kidney, liver, pancreas, skeletal muscle, testis and CD4 T cells, for both human and mouse. We integrated multiple sources of expression data to compile sets of transcripts with strong evidence for tissue-specific regulation. The analysis of the promoters corresponding to these sets produced a catalog of predicted tissue-specific motifs and modules, and cis-regulatory elements. Predicted regulatory interactions are supported by statistical evidence, and provide a foundation for targeted experiments that will improve our understanding of tissue-specific regulatory networks. In a broader context, methods used to construct the catalog provide a model for the analysis of genomic regions that regulate differentially expressed genes. Nature Publishing Group 2007-01-16 /pmc/articles/PMC1800356/ /pubmed/17224917 http://dx.doi.org/10.1038/msb4100114 Text en Copyright © 2007, EMBO and Nature Publishing Group
spellingShingle Report
Smith, Andrew D
Sumazin, Pavel
Zhang, Michael Q
Tissue-specific regulatory elements in mammalian promoters
title Tissue-specific regulatory elements in mammalian promoters
title_full Tissue-specific regulatory elements in mammalian promoters
title_fullStr Tissue-specific regulatory elements in mammalian promoters
title_full_unstemmed Tissue-specific regulatory elements in mammalian promoters
title_short Tissue-specific regulatory elements in mammalian promoters
title_sort tissue-specific regulatory elements in mammalian promoters
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800356/
https://www.ncbi.nlm.nih.gov/pubmed/17224917
http://dx.doi.org/10.1038/msb4100114
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