Dissection of zebrafish <i>shha</i> function using site-specific targeting with a Cre-dependent genetic switch.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28513431.
- Also identified by DOI 10.7554/eLife.24635 and PMC identifier 5435461.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Despite the extensive use of zebrafish as a model organism in developmental biology and regeneration research, genetic techniques enabling conditional analysis of gene function are limited. In this study, we generated <i>Zwitch</i>, a Cre-dependent invertible gene-trap cassette, enabling the establishment of conditional alleles in zebrafish by generating intronic insertions via in vivo homologous recombination. To demonstrate the utility of <i>Zwitch</i>, we generated a conditional <i>sonic hedgehog a</i> (<i>shha</i>) allele. Homozygous <i>shha</i> mutants developed normally; however, <i>shha</i> mutant embryos globally expressing Cre exhibited strong reductions in endogenous <i>shha</i> and <i>shha</i> target gene mRNA levels and developmental defects associated with null <i>shha</i> mutations. Analyzing a conditional <i>shha</i> mutant generated using an epicardium-specific inducible Cre driver revealed unique roles for epicardium-derived Shha in myocardial proliferation during heart development and regeneration. <i>Zwitch</i> will extend the utility of zebrafish in organ development and regeneration research and might be applicable to other model organisms.
Medical subject headings
- Gene Targeting
- Heart
- Hedgehog Proteins
- Zebrafish
- Zebrafish Proteins