The gene regulatory basis of genetic compensation during neural crest induction

Dooley, C.M., Wali, N., Sealy, I.M., White, R.J., Stemple, D.L., Collins, J.E., Busch-Nentwich, E.M.
PLoS Genetics   15: e1008213 (Journal)
Registered Authors
Busch-Nentwich, Elisabeth, Dooley, Christopher, Stemple, Derek L.
MeSH Terms
  • Animals
  • Cell Differentiation/genetics
  • Cell Lineage/genetics
  • Embryo, Nonmammalian
  • Embryonic Development/genetics*
  • Gene Expression Regulation, Developmental/genetics
  • Gene Regulatory Networks/genetics
  • Melanocytes/metabolism
  • Microphthalmia-Associated Transcription Factor/genetics
  • Neural Crest/growth & development*
  • Neural Crest/metabolism
  • Pigmentation/genetics
  • Protein Serine-Threonine Kinases/genetics
  • SOXE Transcription Factors/genetics*
  • Transcription Factor AP-2/genetics*
  • Zebrafish/genetics
  • Zebrafish/growth & development
  • Zebrafish Proteins/genetics*
31199790 Full text @ PLoS Genet.
The neural crest (NC) is a vertebrate-specific cell type that contributes to a wide range of different tissues across all three germ layers. The gene regulatory network (GRN) responsible for the formation of neural crest is conserved across vertebrates. Central to the induction of the NC GRN are AP-2 and SoxE transcription factors. NC induction robustness is ensured through the ability of some of these transcription factors to compensate loss of function of gene family members. However the gene regulatory events underlying compensation are poorly understood. We have used gene knockout and RNA sequencing strategies to dissect NC induction and compensation in zebrafish. We genetically ablate the NC using double mutants of tfap2a;tfap2c or remove specific subsets of the NC with sox10 and mitfa knockouts and characterise genome-wide gene expression levels across multiple time points. We find that compensation through a single wild-type allele of tfap2c is capable of maintaining early NC induction and differentiation in the absence of tfap2a function, but many target genes have abnormal expression levels and therefore show sensitivity to the reduced tfap2 dosage. This separation of morphological and molecular phenotypes identifies a core set of genes required for early NC development. We also identify the 15 somites stage as the peak of the molecular phenotype which strongly diminishes at 24 hpf even as the morphological phenotype becomes more apparent. Using gene knockouts, we associate previously uncharacterised genes with pigment cell development and establish a role for maternal Hippo signalling in melanocyte differentiation. This work extends and refines the NC GRN while also uncovering the transcriptional basis of genetic compensation via paralogues.
Genes / Markers
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Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes