Literature DB >> 11156606

The transcription factor Sox10 is a key regulator of peripheral glial development.

S Britsch1, D E Goerich, D Riethmacher, R I Peirano, M Rossner, K A Nave, C Birchmeier, M Wegner.   

Abstract

The molecular mechanisms that determine glial cell fate in the vertebrate nervous system have not been elucidated. Peripheral glial cells differentiate from pluripotent neural crest cells. We show here that the transcription factor Sox10 is a key regulator in differentiation of peripheral glial cells. In mice that carry a spontaneous or a targeted mutation of Sox10, neuronal cells form in dorsal root ganglia, but Schwann cells or satellite cells are not generated. At later developmental stages, this lack of peripheral glial cells results in a severe degeneration of sensory and motor neurons. Moreover, we show that Sox10 controls expression of ErbB3 in neural crest cells. ErbB3 encodes a Neuregulin receptor, and down-regulation of ErbB3 accounts for many changes in development of neural crest cells observed in Sox10 mutant mice. Sox10 also has functions not mediated by ErbB3, for instance in the melanocyte lineage. Phenotypes observed in heterozygous mice that carry a targeted Sox10 null allele reproduce those observed in heterozygous Sox10(Dom) mice. Haploinsufficiency of Sox10 can thus cause pigmentation and megacolon defects, which are also observed in Sox10(Dom)/+ mice and in patients with Waardenburg-Hirschsprung disease caused by heterozygous SOX10 mutations.

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Year:  2001        PMID: 11156606      PMCID: PMC312607          DOI: 10.1101/gad.186601

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  42 in total

Review 1.  Role of neuregulins in glial cell development.

Authors:  K Adlkofer; C Lai
Journal:  Glia       Date:  2000-01-15       Impact factor: 7.452

2.  Cysteine-rich domain isoforms of the neuregulin-1 gene are required for maintenance of peripheral synapses.

Authors:  D Wolpowitz; T B Mason; P Dietrich; M Mendelsohn; D A Talmage; L W Role
Journal:  Neuron       Date:  2000-01       Impact factor: 17.173

3.  Rescue of the cardiac defect in ErbB2 mutant mice reveals essential roles of ErbB2 in peripheral nervous system development.

Authors:  J K Morris; W Lin; C Hauser; Y Marchuk; D Getman; K F Lee
Journal:  Neuron       Date:  1999-06       Impact factor: 17.173

4.  Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos.

Authors:  R P Kapur
Journal:  Pediatr Dev Pathol       Date:  1999 Nov-Dec

5.  Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3.

Authors:  D J Epstein; M Vekemans; P Gros
Journal:  Cell       Date:  1991-11-15       Impact factor: 41.582

6.  A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies.

Authors:  N Bondurand; K Kuhlbrodt; V Pingault; J Enderich; M Sajus; N Tommerup; M Warburg; R C Hennekam; A P Read; M Wegner; M Goossens
Journal:  Hum Mol Genet       Date:  1999-09       Impact factor: 6.150

7.  Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development.

Authors:  M T Woldeyesus; S Britsch; D Riethmacher; L Xu; E Sonnenberg-Riethmacher; F Abou-Rebyeh; R Harvey; P Caroni; C Birchmeier
Journal:  Genes Dev       Date:  1999-10-01       Impact factor: 11.361

8.  The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.

Authors:  E M Southard-Smith; M Angrist; J S Ellison; R Agarwala; A D Baxevanis; A Chakravarti; W J Pavan
Journal:  Genome Res       Date:  1999-03       Impact factor: 9.043

9.  Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation.

Authors:  K Inoue; Y Tanabe; J R Lupski
Journal:  Ann Neurol       Date:  1999-09       Impact factor: 10.422

10.  The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor.

Authors:  C Pusch; E Hustert; D Pfeifer; P Südbeck; R Kist; B Roe; Z Wang; R Balling; N Blin; G Scherer
Journal:  Hum Genet       Date:  1998-08       Impact factor: 4.132

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  319 in total

1.  Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10.

Authors:  C Claus Stolt; Stephan Rehberg; Marius Ader; Petra Lommes; Dieter Riethmacher; Melitta Schachner; Udo Bartsch; Michael Wegner
Journal:  Genes Dev       Date:  2002-01-15       Impact factor: 11.361

2.  Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8.

Authors:  E Sock; K Schmidt; I Hermanns-Borgmeyer; M R Bösl; M Wegner
Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

3.  Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice.

Authors:  Sarah R Anderson; Inyoul Lee; Christine Ebeling; Dennis A Stephenson; Kelsey M Schweitzer; David Baxter; Tara M Moon; Sarah LaPierre; Benjamin Jaques; Derek Silvius; Michael Wegner; Leroy E Hood; George Carlson; Teresa M Gunn
Journal:  Mamm Genome       Date:  2014-11-16       Impact factor: 2.957

Review 4.  New insights into signaling during myelination in zebrafish.

Authors:  Alya R Raphael; William S Talbot
Journal:  Curr Top Dev Biol       Date:  2011       Impact factor: 4.897

Review 5.  Signals that determine Schwann cell identity.

Authors:  K R Jessen; R Mirsky
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

6.  Sox10 is an active nucleocytoplasmic shuttle protein, and shuttling is crucial for Sox10-mediated transactivation.

Authors:  Stephan Rehberg; Peter Lischka; Gabi Glaser; Thomas Stamminger; Michael Wegner; Olaf Rosorius
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

7.  The Sox9 transcription factor determines glial fate choice in the developing spinal cord.

Authors:  C Claus Stolt; Petra Lommes; Elisabeth Sock; Marie-Christine Chaboissier; Andreas Schedl; Michael Wegner
Journal:  Genes Dev       Date:  2003-07-01       Impact factor: 11.361

8.  Calcineurin/NFAT signaling is required for neuregulin-regulated Schwann cell differentiation.

Authors:  Shih-Chu Kao; Hai Wu; Jianming Xie; Ching-Pin Chang; Jeffrey A Ranish; Isabella A Graef; Gerald R Crabtree
Journal:  Science       Date:  2009-01-30       Impact factor: 47.728

9.  Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.

Authors:  Nadege Bondurand; Florence Dastot-Le Moal; Laure Stanchina; Nathalie Collot; Viviane Baral; Sandrine Marlin; Tania Attie-Bitach; Irina Giurgea; Laurent Skopinski; William Reardon; Annick Toutain; Pierre Sarda; Anis Echaieb; Marilyn Lackmy-Port-Lis; Renaud Touraine; Jeanne Amiel; Michel Goossens; Veronique Pingault
Journal:  Am J Hum Genet       Date:  2007-10-22       Impact factor: 11.025

10.  Hirschsprung-like disease is exacerbated by reduced de novo GMP synthesis.

Authors:  Jonathan I Lake; Olga A Tusheva; Brittany L Graham; Robert O Heuckeroth
Journal:  J Clin Invest       Date:  2013-11       Impact factor: 14.808

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