

Seville 41013, Spain In multicellular organisms, cis-regulation controls gene expression in space and time. Despite the essential implication of cisregulation in the development and evolution of organisms and in human diseases, our knowledge about regulatory sequences largely derives from analyzing their activity individually and outside their genomic context. Indeed, the contribution of these sequences to the expression of their target genes in their genomic context is still largely unknown. Here we present a novel genetic screen designed to visualize and interrupt gene regulatory landscapes in vertebrates. In this screen, based on the random insertion of an engineered Tol2 transposon carrying a strong insulator separating two fluorescent reporter genes, we isolated hundreds of zebrafish lines containing insertions that disrupt the cis-regulation of tissue-specific expressed genes. We therefore provide a new easy-to-handle tool that will help to disrupt and chart the regulatory activity spread through the vast noncoding regions of the vertebrate genome. © 2014 Bessa et al.
| EMTREE drug terms: | cre recombinasegreen fluorescent proteinred fluorescent protein |
|---|---|
| EMTREE medical terms: | articlechromosomedown regulationembryoenhancer regiongene controlgene expressiongenetic screeninghomozygosityin situ hybridizationinsulator elementinverse polymerase chain reactionLoxP sitemousenonhumannotochordphenotypepriority journalpromoter regionreporter geneSouthern blottingtransposonvertebratezebra fish |
| MeSH: | AnimalsAnimals, Genetically ModifiedDNA Transposable ElementsEnhancer Elements, GeneticFluorescenceGenes, ReporterGenomeHumansInsulator ElementsMiceMutagenesis, InsertionalVertebratesZebrafish |
red fluorescent protein, 251925-26-5
Bessa, J.; Centro Andaluz de Biología Del Desarrollo (CABD, CSIC-Universidad Pablo de Olavide-Junta de Andalucía, Spain;
© Copyright 2014 Elsevier B.V., All rights reserved.