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Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system.

Abstract
Human SOX10 and mouse Sox10 have been cloned and shown to be expressed in the neural crest derivatives that contribute to formation of the peripheral nervous system during embryogenesis. Mutations in Sox10 have been identified as a cause of the Dominant megacolon mouse and Waardenburg-Shah syndrome in human, both of which include defects in the enteric nervous system and pigmentation (and in the latter, sometimes hearing). We have cloned a chick Sox10 ortholog (cSox10) in order to study its role in neural crest cell development. This cDNA reveals a 1383 bp open reading frame encoding 461 amino acids which is highly conserved with human SOX10 and mouse Sox10. In situ hybridization showed cSox10 is expressed in migrating neural crest cells just after the zinc finger transcription factor Slug, but is lost as cells undergo neuronal differentiation in ganglia of the peripheral nervous system. In addition, cSox10 is expressed in the developing otic vesicle, the developing central nervous system and pineal gland.
AuthorsY Cheng, M Cheung, M M Abu-Elmagd, A Orme, P J Scotting
JournalBrain research. Developmental brain research (Brain Res Dev Brain Res) Vol. 121 Issue 2 Pg. 233-41 (Jun 30 2000) ISSN: 0165-3806 [Print] Netherlands
PMID10876038 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA-Binding Proteins
  • High Mobility Group Proteins
  • RNA, Messenger
  • SOX10 protein, human
  • SOXE Transcription Factors
  • Sox10 protein, mouse
  • Transcription Factors
Topics
  • Animals
  • Auditory Pathways (chemistry, embryology, physiology)
  • Central Nervous System (chemistry, embryology, physiology)
  • Chick Embryo
  • Chickens
  • Cloning, Molecular
  • DNA-Binding Proteins (genetics)
  • Gene Expression Regulation, Developmental (physiology)
  • High Mobility Group Proteins (genetics)
  • Hirschsprung Disease (genetics)
  • Humans
  • In Situ Hybridization
  • Mice
  • Molecular Sequence Data
  • Neural Crest (chemistry, embryology, physiology)
  • Neuroglia (chemistry, physiology)
  • Neurons (chemistry, physiology)
  • Pineal Gland (chemistry, embryology, physiology)
  • RNA, Messenger (analysis)
  • SOXE Transcription Factors
  • Sequence Homology, Amino Acid
  • Transcription Factors (genetics)
  • Waardenburg Syndrome (genetics)

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