ZFIN ID: ZDB-PUB-090714-1
Notch and MAML signaling drives Scl-dependent interneuron diversity in the spinal cord
Peng, C.Y., Yajima, H., Burns, C.E., Zon, L.I., Sisodia, S.S., Pfaff, S.L., and Sharma, K.
Date: 2007
Source: Neuron 53(6): 813-827 (Journal)
Registered Authors: Burns (Erter), Caroline, Zon, Leonard I.
Keywords: MOLNEURO, DEVBIO
MeSH Terms:
  • Animals
  • Animals, Genetically Modified
  • Bromodeoxyuridine/metabolism
  • Cell Communication
  • Chick Embryo
  • Electroporation/methods
  • Gene Expression Regulation, Developmental
  • Immunohistochemistry/methods
  • In Situ Hybridization/methods
  • Interneurons/classification
  • Interneurons/metabolism*
  • Mice
  • Models, Biological
  • Nerve Tissue Proteins/genetics
  • Receptors, Notch/metabolism*
  • Signal Transduction/physiology*
  • Spinal Cord/cytology*
  • Trans-Activators/metabolism*
  • Zebrafish
  • Zebrafish Proteins/genetics
PubMed: 17359917 Full text @ Neuron
FIGURES
ABSTRACT
The ventral spinal cord generates multiple inhibitory and excitatory interneuron subtypes from four cardinal progenitor domains (p0, p1, p2, p3). Here we show that cell-cell interactions mediated by the Notch receptor play a critical evolutionarily conserved role in the generation of excitatory v2aIN and inhibitory v2bIN interneurons. Lineage-tracing experiments show that the v2aIN and v2bIN develop from genetically identical p2 progenitors. The p2 daughter cell fate is controlled by Delta4 activation of Notch receptors together with MAML factors. Cells receiving Notch signals activate a transcription factor code that specifies the v2bIN fate, whereas cells deprived of Notch signaling express another code for v2aIN formation. Thus, our study provides insight into the cell-extrinsic signaling that controls combinatorial transcription factor profiles involved in regulating the process of interneuron subtype diversification.
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