PUBLICATION

Generation of an Enhancer-Trapping Vector for Insertional Mutagenesis in Zebrafish

Authors
Liu, C., Song, G., Mao, L., Long, Y., Li, Q., Cui, Z.
ID
ZDB-PUB-151006-5
Date
2015
Source
PLoS One   10: e0139612 (Journal)
Registered Authors
Cui, Zongbin, Li, Qing, Liu, Chunyan, Long, Yong, Song, Guili
Keywords
Embryos, Zebrafish, Gene expression, Polymerase chain reaction, DNA transcription, Transposable elements, Introns, Comparative genomics
MeSH Terms
  • Organ Specificity
  • Pancreas/metabolism
  • Mutagenesis, Insertional*
  • Green Fluorescent Proteins/genetics
  • DNA Transposable Elements/genetics*
  • Animals, Genetically Modified
  • Central Nervous System/metabolism
  • Gene Expression Regulation
  • Kidney/metabolism
  • Real-Time Polymerase Chain Reaction
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Enhancer Elements, Genetic*
  • Genes, Reporter
  • Genes, Synthetic
  • Promoter Regions, Genetic/genetics
  • Zebrafish Proteins/biosynthesis
  • Zebrafish Proteins/genetics
  • Mice
  • Metallothionein/genetics
  • Genetic Vectors/genetics*
  • Animals
  • Crosses, Genetic
(all 23)
PubMed
26436547 Full text @ PLoS One
Abstract
Enhancer trapping (ET) is a powerful approach to establish tissue- or cell-specific reporters and identify expression patterns of uncharacterized genes. Although a number of enhancer-trapping vectors have been developed and a large library of fish lines with distinct tissue- or cell-specific expression of reporter genes have been generated, the specificity and efficiency of trapping vectors need to be improved because of the bias interaction of minimal promoters with genomic enhancers. Accordingly, we generated an enhancer-trapping vector pTME that contains a minimal mouse metallothionein gene (mMTI) promoter upstream of EGFP reporter. In the first round of screening, twelve zebrafish lines that carry a single copy of ET cassettes were characterized to have tissue- or cell-specific EGFP expression. One of the highly conserved noncoding elements near an insertion site of trapping cassettes was characterized as an enhancer that can specifically regulate the expression of EGFP in cells of the central nervous system. In addition, the pTME vector contains a mutation-cassette that is able to effectively block the transcription of an endogenous gene in an ET line with ubiquitous EGFP expression. Thus, the pTME vector can be used as an alternative tool for both enhancer trapping and mutagenesis across a target genome.
Genes / Markers
Marker Marker Type Name
esrrbGENEestrogen-related receptor beta
hs3st3b1bGENEheparan sulfate (glucosamine) 3-O-sulfotransferase 3B1b
kif7GENEkinesin family member 7
mecomGENEMDS1 and EVI1 complex locus
mmd2aGENEmonocyte to macrophage differentiation-associated 2a
napsaGENEnapsin A aspartic peptidase
si:ch211-243g18.3GENEsi:ch211-243g18.3
si:dkey-246i21.1GENEsi:dkey-246i21.1
skor2GENESKI family transcriptional corepressor 2
slc6a1bGENEsolute carrier family 6 member 1b
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Figures
Figure Gallery (7 images)
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
ihb204EtTransgenic Insertion
    ihb205EtTransgenic Insertion
      ihb206EtTransgenic Insertion
        ihb207EtTransgenic Insertion
          ihb208EtTransgenic Insertion
            zf1019EtTransgenic Insertion
              zf1020EtTransgenic Insertion
                zf1021EtTransgenic Insertion
                  zf1022EtTransgenic Insertion
                    zf1023EtTransgenic Insertion
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                      Human Disease / Model
                      No data available
                      Sequence Targeting Reagents
                      No data available
                      Fish
                      Antibodies
                      No data available
                      Orthology
                      No data available
                      Engineered Foreign Genes
                      Marker Marker Type Name
                      EGFPEFGEGFP
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                      Mapping
                      No data available