TRACER: a resource to study the regulatory architecture of the mouse genome

被引:12
作者
Chen, Chao-Kung [1 ]
Symmons, Orsolya [2 ]
Uslu, Veli Vural [2 ]
Tsujimura, Taro [2 ]
Ruf, Sandra [2 ]
Smedley, Damian [1 ]
Spitz, Francois [2 ]
机构
[1] European Bioinformat Inst, European Mol Biol Lab, Cambridge CB10 1SD, England
[2] European Mol Biol Lab, Dev Biol Unit, D-69012 Heidelberg, Germany
来源
BMC GENOMICS | 2013年 / 14卷
关键词
Gene regulation and expression; Genome organisation; Regulatory landscapes; Chromosomal engineering; Mouse models of human structural variation; THUMB-POLYSYNDACTYLY SYNDROME; CONSERVED NONCODING ELEMENTS; SLEEPING-BEAUTY TRANSPOSON; GLOBAL CONTROL REGION; EMBRYONIC STEM-CELLS; LONG-RANGE; GENE-EXPRESSION; CHROMATIN INTERACTIONS; ENHANCER DETECTION; SHH ENHANCER;
D O I
10.1186/1471-2164-14-215
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
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页数:13
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