A direct role for Sox10 in specification of neural crest-derived sensory neurons
Abstract
sox10 is necessary for development of neural and pigment cell derivatives of the neural crest (NC). However, whereas a direct role for Sox10 activity has been established in pigment and glial lineages, this is more controversial in NC-derived sensory neurons of the dorsal root ganglia (DRGs). We proposed that sox10 functioned in specification of sensory neurons, whereas others suggested that sensory neuronal defects were merely secondary to absence of glia. Here we provide evidence that in zebrafish,early DRG sensory neuron survival is independent of differentiated glia. Critically, we demonstrate that Sox10 is expressed transiently in the sensory neuron lineage, and specifies sensory neuron precursors by regulating the proneural gene neurogenin1. Consistent with this, we have isolated a novel sox10 mutant that lacks glia and yet displays a neurogenic DRG phenotype. In conjunction with previous findings, these data establish the generality of our model of Sox10 function in NC fate specification.
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sox10 and sox9b have been shown to be functionally redundant in DRG sensory neuron development.
“As members of the same SoxE group, it is not surprising that sox10 and sox9b have been shown to be functionally redundant in DRG sensory neuron development [22].”
From The MITF paralog tfec is required in neural crest development for fate specification of the iridophore lineage from a multipotent pigment cell progenitor (2021) · cites this paper as [22]
Sox10 and Sox9b have previously been reported to act redundantly during zebrafish development.
“Sox10 and Sox9b have previously been reported to act redundantly during zebrafish development [13, 22].”
From The MITF paralog tfec is required in neural crest development for fate specification of the iridophore lineage from a multipotent pigment cell progenitor (2021) · cites this paper as [22]
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Self-citation
- Authors
- Carney, T. J., Dutton, K. A., Greenhill, E., Delfino-Machín, M., Dufourcq, P., Blader, P., & Kelsh, R. N.
- Affiliations
- University of Bath (GB)
- Centre for Regenerative Medicine, Developmental Biology Programme, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
- Université Toulouse III - Paul Sabatier (FR)
- Corresponding author
- Kelsh, Robert N.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2006-12-01
- Volume
- 133
- Issue
- 23
- Pages
- 4619-4630
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2020788680
- Cited by
- 307
- References
- 0
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 14 · 2023: 15 · 2022: 15 · 2021: 36 · 2020: 13 · 2019: 17 · 2018: 21 · 2017: 14 · 2016: 14 · 2015: 14 · 2014: 11 · 2013: 24 · 2012: 19
- FWCI
- 3.67
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Development (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Wellcome Trust
- Biotechnology and Biological Sciences Research Council (BB/D000440/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Surgery › Congenital gastrointestinal and neural anomalies
- Keywords
- SOX10, neural crest, sensory neurons, dorsal root ganglia, neurogenin1, proneural genes, sensory neuron specification, sensory neuron survival, zebrafish
- MeSH terms
- Alleles, Animals, Base Sequence, Carrier Proteins, Cell Survival, DNA, Ganglia, Spinal, High Mobility Group Proteins, Models, Neurological, Mutation, Nerve Tissue Proteins, Neural Crest, Neurons, Afferent, Phenotype, Promoter Regions, Genetic, Recombinant Fusion Proteins, Stem Cells, Zebrafish, Gene Expression Regulation, Developmental, Zebrafish Proteins, Animals, Genetically Modified, Green Fluorescent Proteins, Basic Helix-Loop-Helix Proteins, SOXE Transcription Factors
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