Establishing neural crest identity: a gene regulatory recipe
Open accessAbstract
The neural crest is a stem/progenitor cell population that contributes to a wide variety of derivatives, including sensory and autonomic ganglia, cartilage and bone of the face and pigment cells of the skin. Unique to vertebrate embryos, it has served as an excellent model system for the study of cell behavior and identity owing to its multipotency, motility and ability to form a broad array of cell types. Neural crest development is thought to be controlled by a suite of transcriptional and epigenetic inputs arranged hierarchically in a gene regulatory network. Here, we examine neural crest development from a gene regulatory perspective and discuss how the underlying genetic circuitry results in the features that define this unique cell population.
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Our data formally establish tfec as a member of the GRN governing maintenance of NCC progenitors.
“Our data formally establish tfec as a member of the GRN governing maintenance of NCC progenitors [41].”
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 [41]
The study identifies upstream regulators of tfec in multipotent premigratory NC.
“Importantly, we identify its upstream regulators in the multipotent premigratory NC, thus for the first time placing the transcription factor in context in the NCC specification GRN [41].”
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 [41]
The neural crest specifier genes and Regulatory interactions in the migratory neural crest sections discuss regulators and premigratory neural crest, but the passages found do not identify upstream regulators of tfec. Searches for “tfec” and “tfec upstream regulators premigratory neural crest” found no passage addressing that specific claim. In the citing sentence, “we identify” also describes the citing authors’ own finding, rather than explicitly attributing it to this review. (LLM, conf=0.76)
Experimental — accuracy not yet measuredNR2F1 plays a role in regulating neural crest specifier genes and has undergone selection in AMH.
“NR2F1, which plays a role in regulating neural crest specifier genes and has undergone selection in AMH [64, 65]”
From Self-domestication in Homo sapiens: Insights from comparative genomics (2017) · cites this paper as [65]
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- Authors
- Simões-Costa, M., & Bronner, M. E.
- Affiliations
- California Institute of Technology (US)
- Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA
- ORCID
- Simões-Costa, Marcos
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2015-01-15
- Volume
- 142
- Issue
- 2
- Pages
- 242-257
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC4302844
- OpenAlex
- W2134374915
- Cited by
- 649
- References
- 162
- Citations by year
- 2026: 48 · 2025: 56 · 2024: 56 · 2023: 54 · 2022: 45 · 2021: 76 · 2020: 63 · 2019: 69 · 2018: 66 · 2017: 43 · 2016: 52 · 2015: 21
- FWCI
- 5.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Dental and Craniofacial Research (K99DE024232)
- 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
- neural crest, neural crest development, cell identity, gene regulatory networks, transcriptional regulation, epigenetic regulation, multipotency, cell motility, sensory ganglia, autonomic ganglia, pigment cells, stem/progenitor cells
- MeSH terms
- Animals, Cell Differentiation, Models, Biological, Neural Crest, Vertebrates, Gene Expression Regulation, Developmental, Epigenesis, Genetic, Gene Regulatory Networks
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