Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates

Development

Volumn 128, Issue 21, 2001, Pages 4113-4125

  Dutton, K A ^a   Pauliny, A ^a   Lopes, S S ^a   Elworthy, S ^a   Carney, T J ^a   Rauch, J ^a   Geisler, R ^a   Haffter, P ^a   Kelsh, R N ^a  

^a University of Bath   (United Kingdom)

Author keywords

Apoptosis; Danio rerio; Hirschsprung's disease; Melanophore; Pigment cells; Waardenburg Shah syndrome

Indexed keywords

GENE PRODUCT; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR SOX10; UNCLASSIFIED DRUG;

ALLELE; ANIMAL CELL; APOPTOSIS; ARTICLE; BIOLOGICAL MODEL; CELL COUNT; CELL DEATH; CELL FATE; CELL MIGRATION; CELL MUTANT; CONTROLLED STUDY; EMBRYO; FERTILIZATION; GENE DISRUPTION; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC CODE; HIRSCHSPRUNG DISEASE; INTESTINE INNERVATION; LESIONS AND DEFECTS; MELANOPHORE; MESENCHYME; MOLECULAR BIOLOGY; MUTANT; NERVE CELL DIFFERENTIATION; NEURAL CREST; NEURAL CREST CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PHENOTYPE; PIGMENT CELL; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; WAARDENBURG SYNDROME; ZEBRA FISH;

AMINO ACID SEQUENCE; ANIMALS; APOPTOSIS; CARRIER PROTEINS; CELL DIFFERENTIATION; CELL MOVEMENT; CHROMOSOME MAPPING; CLONING, MOLECULAR; DNA-BINDING PROTEINS; EMBRYO, NONMAMMALIAN; EMBRYONIC INDUCTION; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HIGH MOBILITY GROUP PROTEINS; HIRSCHSPRUNG DISEASE; LINKAGE (GENETICS); MELANOPHORES; MESODERM; MOLECULAR SEQUENCE DATA; MUTATION; NEURAL CREST; PIGMENTATION DISORDERS; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTORS; ZEBRAFISH; ZEBRAFISH PROTEINS;

ANIMALIA; DANIO RERIO; MELANOPHORA;

EID: 0035173002     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (64)

1. Combinatorial expression of three zebrafish genes related to distalless: Part of a homeobox gene code for the head
2. Cell lineage determination and the control of neuronal identity in the crest
3. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
4. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
5. The neurocristopathies: A unifying concept of disease arising in neural crest maldevelopment
6. Expression of the SOX10 gene during human development
7. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome
8. The transcription factor Sox10 is a key regulator of peripheral glial development
9. A morpholino phenocopy of the colourless mutant
10. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
11. The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio
12. Laser-induced gene expression in specific cells of transgenic zebrafish
13. Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease
14. A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
15. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
16. Radiation hybrid mapping of the zebrafish genome
17. Developmental activation of the capability to undergo checkpoint-induced apoptosis in the early zebrafish embryo
18. Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos
19. Zebrafish pigmentation mutations and the processes of neural crest development
20. The zebrafish colourless gene regulates development of non-ectomesenchymal neural crest derivatives
21. Expression of zebrafish fkd6 in neural crest-derived glia
22. Genetic analysis of melanophore development in zebrafish embryos
23. Stages of embryonic development of the zebrafish
24. A reference cross DNA panel for zebrafish (Danio rerio) anchored with simple sequence length polymorphisms
25. Sox10, a novel transcriptional modulator in glial cells
26. Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
27. Association of megacolon with a new dominant spotting gene (Dom) in the mouse
28. Direct regulation of the microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2
29. Nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate
30. Cell type-specific activation of neuronal nicotinic acetylcholine receptor subunit genes by Sox10
31. Mutations affecting development of the zebrafish ear
32. Hu neuronal proteins are expressed in proliferating neurogenic cells
33. The development of piebald spotting in mice
34. An experimental investigation of pattern development in lethal spotting and belted mouse embryos
35. Fork head domain genes in zebrafish
36. Melanocyte development in vivo and in neural crest cell cultures: Crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription
37. Zebrafish sparse corresponds to an orthologue of c-kit and is required for the morphogenesis of a subpopulation of melanocytes, but is not essential for hematopoiesis or primordial germ cell development
38. An orthologue of the kit-related gene fms is required for development of neural crest-derived xanthophores and a subpopulation of adult melanocytes in the zebrafish, Danio rerio
39. The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
40. The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences
41. Sox genes find their feet
42. SOX10 mutations in patients with Waardenburg-Hirschsprung disease
43. Transcription factor hierarchy in Waardenburg syndrome: Regulation of MITF expression by SOX10 and PAX3
44. A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
45. The SOX10/Sox10 gene from human and mouse: Sequence, expression, and transactivation by the encoded HMG domain transcription factor
46. Restriction of neural crest cell fate in the trunk of the embryonic zebrafish
47. Segregation and early dispersal of neural crest cells in the embryonic zebrafish
48. Wnt5 is required for tail formation in the zebrafish embryo
49. Development and Death of Zebrafish Rohon-Beard Spinal Sensory Neurons
50. Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo
51. No tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene
52. Trunk neural crest origin of caudal fin mesenchyme in the zebrafish Brachydanio rerio
53. Sox10 mutation disrupts neural crest development in DOM Hirschsprung mouse model
54. The Sox10(Dom) mouse: Modeling the genetic variation of Waardenburg-Shah (WS4) syndrome
55. Quartet puzzling: A quartet maximum-likelihood method for reconstructing tree topologies
56. Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics
57. Estimation of the number of nucleotide substitutions in the control region of mitochondrial-DNA in humans and chimpanzees
58. The CLUSTALwindows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools
59. Regulation of microphthalmia-associated transcription factor gene by the waardenburg syndrome type 4 Gene, Sox10
60. From head to toes: The multiple facets of Sox proteins
61. Soluble and cell-bound forms of steel factor activity play distinct roles in melanocyte precursor dispersal and survival on the lateral neural crest migration pathway
62. Receptor tyrosine kinase-dependent neural crest migration in response to differentially localized growth factors
63. Developmental-specific activity of the FGF-4 enhancer requires the synergistic action of Sox2 and Oct-3