Cre-inducible site-specific recombination in zebrafish oligodendrocytes

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

BACKGROUND: The conditional Cre/lox system has recently emerged as a valuable tool for studies on both embryonic and adult Zebrafish. Temporal control and site-specific recombination are achieved by using the ligand-inducible CreERT2 and administration of the drug tamoxifen (TAM) or its active metabolite, 4-Hydroxytamoxifen (4-OHT).

RESULTS: Here we report the generation of a transgenic Zebrafish line, which expresses an mCherry-tagged variant of CreERT2 under the control of the myelin basic protein a (mbpa) promoter. Our analysis shows that larval and adult expression of the transgene recapitulates the endogenous mbpa expression pattern in oligodendrocytes. Furthermore, combination with a Cre-dependent EGFP reporter results in EGFP-expressing oligodendrocytes in the spinal cord, brain, and optic nerve in TAM- or 4-OHT-treated larvae and 4-month-old fish, but not in untreated controls.

CONCLUSIONS: The transgenic Zebrafish line Tg(mbpa:mCherry-T2A-CreERT2 ) elicits CreERT2 expression specifically in myelinating glia cells. Cre-inducible targeted recombination of genes in oligodendrocytes will be useful to elucidate cellular and molecular mechanisms of myelination in vivo during development (myelination) and regeneration (remyelination) after injury to the central nervous system (CNS). It will also allow targeted expression and overexpression of genes of interest (transgenes) in oligodendrocytes at defined developmental and adult stages. Developmental Dynamics 246:41-49, 2017. © 2016 Wiley Periodicals, Inc.

Details

Original languageEnglish
Pages (from-to)41-49
Number of pages9
JournalDevelopmental Dynamics
Volume246
Issue number1
Publication statusPublished - Jan 2017
Peer-reviewedYes

External IDs

Scopus 84991072775
ORCID /0000-0003-0283-0211/work/142257337

Keywords

Research priority areas of TU Dresden

Keywords

  • Animals, Animals, Genetically Modified, Demyelinating Diseases, Gene Expression Regulation, Developmental, Genes, Reporter, Integrases/metabolism, Myelin Basic Protein/genetics, Myelin Sheath/metabolism, Oligodendroglia/metabolism, Promoter Regions, Genetic, Recombination, Genetic, Transgenes, Zebrafish/embryology