

The identification and characterization of the regulatory activity of genomic sequences is crucial for understanding how the information contained in genomes is translated into cellular function. The cis-regulatory sequences control when, where, and how much genes are transcribed and can activate (enhancers) or repress (silencers) gene expression. Here, we describe a novel Tol2 transposon-based vector for assessing enhancer activity in the zebrafish (Danio rerio). This Zebrafish Enhancer Detector (ZED) vector harbors several key improvements, among them a sensitive and specific minimal promoter chosen for optimal enhancer activity detection, insulator sequences to shield the minimal promoter from position effects, and a positive control for transgenesis. Additionally, we demonstrate that highly conserved noncoding sequences homologous between humans and zebrafish largely with enhancer activity largely retain their tissue-specific enhancer activity during vertebrate evolution. More strikingly, insulator sequences from mouse and chicken, but not conserved in zebrafish, maintain their insulator capacity when tested in this model. © 2009 Wiley-Liss, Inc.
| EMTREE drug terms: | proteinprotein Tol2unclassified drug |
|---|---|
| EMTREE medical terms: | animal experimentarticlecontrolled studyenhancer regiongene controlgene expressiongene sequencegene vectorgenomeinsulator elementnonhumanpriority journalpromoter regionsensitivity and specificitysequence homologytransgenicstransposonzebra fishzebrafish enhancer detection vector |
| MeSH: | AnimalsAnimals, Genetically ModifiedEnhancer Elements, GeneticGene Transfer TechniquesGenetic VectorsMiceZebrafish |
| Species Index: | Danio rerioVertebrata |
protein, 67254-75-5
Bessa, J.; Centro Andaluz de Biología del Desarrollo (CABD), CSIC-Universidad Pablo de Olavide, Campus UPO, Ctra. de Utrera km1, Spain;
© Copyright 2009 Elsevier B.V., All rights reserved.
© MEDLINE® is the source for the MeSH terms of this document.