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TRACER: a resource to study the regulatory architecture of the mouse genome
BACKGROUND: Mammalian genes are regulated through the action of multiple regulatory elements, often distributed across large regions. The mechanisms that control the integration of these diverse inputs into specific gene expression patterns are still poorly understood. New approaches enabling the di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618316/ https://www.ncbi.nlm.nih.gov/pubmed/23547943 http://dx.doi.org/10.1186/1471-2164-14-215 |
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author | Chen, Chao-Kung Symmons, Orsolya Uslu, Veli Vural Tsujimura, Taro Ruf, Sandra Smedley, Damian Spitz, François |
author_facet | Chen, Chao-Kung Symmons, Orsolya Uslu, Veli Vural Tsujimura, Taro Ruf, Sandra Smedley, Damian Spitz, François |
author_sort | Chen, Chao-Kung |
collection | PubMed |
description | BACKGROUND: Mammalian genes are regulated through the action of multiple regulatory elements, often distributed across large regions. The mechanisms that control the integration of these diverse inputs into specific gene expression patterns are still poorly understood. New approaches enabling the dissection of these mechanisms in vivo are needed. RESULTS: Here, we describe TRACER (http://tracerdatabase.embl.de), a resource that centralizes information from a large on-going functional exploration of the mouse genome with different transposon-associated regulatory sensors. Hundreds of insertions have been mapped to specific genomic positions, and their corresponding regulatory potential has been documented by analysis of the expression of the reporter sensor gene in mouse embryos. The data can be easily accessed and provides information on the regulatory activities present in a large number of genomic regions, notably in gene-poor intervals that have been associated with human diseases. CONCLUSIONS: TRACER data enables comparisons with the expression pattern of neighbouring genes, activity of surrounding regulatory elements or with other genomic features, revealing the underlying regulatory architecture of these loci. TRACER mouse lines can also be requested for in vivo transposition and chromosomal engineering, to analyse further regions of interest. |
format | Online Article Text |
id | pubmed-3618316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36183162013-04-07 TRACER: a resource to study the regulatory architecture of the mouse genome Chen, Chao-Kung Symmons, Orsolya Uslu, Veli Vural Tsujimura, Taro Ruf, Sandra Smedley, Damian Spitz, François BMC Genomics Database BACKGROUND: Mammalian genes are regulated through the action of multiple regulatory elements, often distributed across large regions. The mechanisms that control the integration of these diverse inputs into specific gene expression patterns are still poorly understood. New approaches enabling the dissection of these mechanisms in vivo are needed. RESULTS: Here, we describe TRACER (http://tracerdatabase.embl.de), a resource that centralizes information from a large on-going functional exploration of the mouse genome with different transposon-associated regulatory sensors. Hundreds of insertions have been mapped to specific genomic positions, and their corresponding regulatory potential has been documented by analysis of the expression of the reporter sensor gene in mouse embryos. The data can be easily accessed and provides information on the regulatory activities present in a large number of genomic regions, notably in gene-poor intervals that have been associated with human diseases. CONCLUSIONS: TRACER data enables comparisons with the expression pattern of neighbouring genes, activity of surrounding regulatory elements or with other genomic features, revealing the underlying regulatory architecture of these loci. TRACER mouse lines can also be requested for in vivo transposition and chromosomal engineering, to analyse further regions of interest. BioMed Central 2013-04-02 /pmc/articles/PMC3618316/ /pubmed/23547943 http://dx.doi.org/10.1186/1471-2164-14-215 Text en Copyright © 2013 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Chen, Chao-Kung Symmons, Orsolya Uslu, Veli Vural Tsujimura, Taro Ruf, Sandra Smedley, Damian Spitz, François TRACER: a resource to study the regulatory architecture of the mouse genome |
title | TRACER: a resource to study the regulatory architecture of the mouse genome |
title_full | TRACER: a resource to study the regulatory architecture of the mouse genome |
title_fullStr | TRACER: a resource to study the regulatory architecture of the mouse genome |
title_full_unstemmed | TRACER: a resource to study the regulatory architecture of the mouse genome |
title_short | TRACER: a resource to study the regulatory architecture of the mouse genome |
title_sort | tracer: a resource to study the regulatory architecture of the mouse genome |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618316/ https://www.ncbi.nlm.nih.gov/pubmed/23547943 http://dx.doi.org/10.1186/1471-2164-14-215 |
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