PUBLICATION

Redefining retinoic acid receptor expression in zebrafish embryos using Hybridization Chain Reaction

Authors
Gray, R., Lovely, C.B.
ID
ZDB-PUB-241204-9
Date
2024
Source
Differentiation; research in biological diversity   140: 100822 (Journal)
Registered Authors
Lovely, Ben
Keywords
Cranial neural crest, Development, Endoderm, Retinoic acid, Retinoic acid receptor, Zebrafish
MeSH Terms
  • Tretinoin*/metabolism
  • Tretinoin*/pharmacology
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
  • Gene Expression Regulation, Developmental*
  • Zebrafish*/embryology
  • Zebrafish*/genetics
  • Embryo, Nonmammalian/metabolism
  • Animals, Genetically Modified
  • Signal Transduction/genetics
  • Animals
  • Neural Crest*/cytology
  • Neural Crest*/growth & development
  • Neural Crest*/metabolism
  • Receptors, Retinoic Acid*/genetics
  • Receptors, Retinoic Acid*/metabolism
  • Retinoid X Receptors/genetics
  • Retinoid X Receptors/metabolism
  • Endoderm/cytology
  • Endoderm/metabolism
PubMed
39627912 Full text @ Differentiation
Abstract
Retinoic Acid (RA) is the key signaling molecule during embryonic development with the RA pathway playing multiple roles in throughout development. Previous work has shown RA signaling to be key in development of the craniofacial skeleton. RA signaling is driven by RA binding to the nuclear transcription factors, retinoic acid receptor (RAR) and retinoic X receptor (RXR). RARs and RXR heterodimerize to bind specific DNA sequences known as retinoic acid response elements or RAREs. Though the genes that code for these receptors are known to be involved during craniofacial development, in which tissues they are expressed remains uncharacterized, varying temporally and spatially. To address this, we used Hybridization Chain Reaction (HCR) to fluorescently visualize rar and rxr mRNA expression in tissue-specific transgenic zebrafish embryos. Here, we show the overall and tissue-specific expression of each receptor in the pharyngeal endoderm and Cranial Neural Crest Cells (CNCC), two cell types that have been shown to be sensitive to RA perturbations. Here we show that the expression of many of the rar/rxr genes overlap with the endoderm-specific sox17:eGFP and/or the CNCC-specific sox10:eGFP transgenic lines between 12 and 32 h post fertilization; time points that capture CNCC and endoderm migration and morphogenesis.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping