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Mammalian achaete-scute and atonal homologs regulate neuronal versus glial fate determination in the central nervous system.

Whereas vertebrate achaete-scute complex (as-c) and atonal (ato) homologs are required for neurogenesis, their neuronal determination activities in the central nervous system (CNS) are not yet supported by loss-of-function studies, probably because of genetic redundancy. Here, to address this problem, we generated mice double mutant for the as-c homolog Mash1 and the ato homolog Math3. Whereas in Mash1 or Math3 single mutants neurogenesis is only weakly affected, in the double mutants tectal neurons, two longitudinal columns of hindbrain neurons and retinal bipolar cells were missing and, instead, those cells that normally differentiate into neurons adopted the glial fate. These results indicated that Mash1 and Math3 direct neuronal versus glial fate determination in the CNS and raised the possibility that downregulation of these bHLH genes is one of the mechanisms to initiate gliogenesis.

Pubmed ID: 11032813


  • Tomita K
  • Moriyoshi K
  • Nakanishi S
  • Guillemot F
  • Kageyama R


The EMBO journal

Publication Data

October 16, 2000

Associated Grants


Mesh Terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Brain
  • Cell Differentiation
  • Central Nervous System
  • DNA-Binding Proteins
  • Gene Deletion
  • Gene Expression Regulation, Developmental
  • Genes, Homeobox
  • Helix-Loop-Helix Motifs
  • Immunohistochemistry
  • In Situ Hybridization
  • Mice
  • Mice, Knockout
  • Nerve Tissue Proteins
  • Neuroglia
  • Neurons
  • Organ Culture Techniques
  • RNA, Messenger
  • Retina
  • Sequence Homology, Amino Acid
  • Transcription Factors