Show simple item record

dc.creatorBalciunas, D
dc.creatorDavidson, AE
dc.creatorSivasubbu, S
dc.creatorHermanson, SB
dc.creatorWelle, Z
dc.creatorEkker, SC
dc.date.accessioned2021-02-01T22:29:15Z
dc.date.available2021-02-01T22:29:15Z
dc.date.issued2004-09-03
dc.identifier.issn1471-2164
dc.identifier.issn1471-2164
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/5638
dc.identifier.other15347431 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/5656
dc.description.abstractBackground: Among functional elements of a metazoan gene, enhancers are particularly difficult to find and annotate. Pioneering experiments in Drosophila have demonstrated the value of enhancer "trapping" using an invertebrate to address this functional genomics problem. Results: We modulated a Sleeping Beauty transposon-based transgenesis cassette to establish an enhancer trapping technique for use in a vertebrate model system, zebrafish Danio rerio. We established 9 lines of zebrafish with distinct tissue- or organ-specific GFP expression patterns from 90 founders that produced GFP-expressing progeny. We have molecularly characterized these lines and show that in each line, a specific GFP expression pattern is due to a single transposition event. Many of the insertions are into introns of zebrafish genes predicted in the current genome assembly. We have identified both previously characterized as well as novel expression patterns from this screen. For example, the ET7 line harbors a transposon insertion near the mkp3 locus and expresses GFP in the midbrain-hindbrain boundary, forebrain and the ventricle, matching a subset of the known FGF8-dependent mkp3 expression domain. The ET2 line, in contrast, expresses GFP specifically in caudal primary motoneurons due to an insertion into the poly(ADPribose) glycohydrolase (PARG) locus. This surprising expression pattern was confirmed using in situ hybridization techniques for the endogenous PARG mRNA, indicating the enhancer trap has replicated this unexpected and highly localized PARG expression with good fidelity. Finally, we show that it is possible to excise a Sleeping Beauty transposon from a genomic location in the zebrafish germline. Conclusions: This genomics tool offers the opportunity for large-scale biological approaches combining both expression and genomic-level sequence analysis using as a template an entire vertebrate genome. © 2004 Balciunas et al; licensee BioMed Central Ltd.
dc.format.extent62-
dc.language.isoen
dc.relation.haspartBMC Genomics
dc.relation.isreferencedbySpringer Science and Business Media LLC
dc.rightsCC BY
dc.subjectAnimals
dc.subjectDNA Transposable Elements
dc.subjectEmbryonic Development
dc.subjectEnhancer Elements, Genetic
dc.subjectGene Transfer Techniques
dc.subjectGenomics
dc.subjectGerm Cells
dc.subjectGlycoside Hydrolases
dc.subjectGreen Fluorescent Proteins
dc.subjectIn Situ Hybridization
dc.subjectMotor Neurons
dc.subjectPilot Projects
dc.subjectPolymerase Chain Reaction
dc.subjectPromoter Regions, Genetic
dc.subjectSequence Analysis, DNA
dc.subjectZebrafish
dc.titleEnhancer trapping in zebrafish using the Sleeping Beauty transposon
dc.typeArticle
dc.type.genreReview
dc.type.genreJournal
dc.relation.doi10.1186/1471-2164-5-62
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.creator.orcidBalciunas, Darius|0000-0003-1938-3243
dc.date.updated2021-02-01T22:29:11Z
refterms.dateFOA2021-02-01T22:29:15Z


Files in this item

Thumbnail
Name:
Enhancer trapping in zebrafish ...
Size:
2.123Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record