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Timing mechanism of sexually dimorphic nervous system differentiation.

Laura PereiraFlorian AeschimannChen WangHannah LawsonEsther Serrano-SaizDouglas S PortmanHelge GroßhansOliver Hobert
Published in: eLife (2019)
The molecular mechanisms that control the timing of sexual differentiation in the brain are poorly understood. We found that the timing of sexually dimorphic differentiation of postmitotic, sex-shared neurons in the nervous system of the Caenorhabditis elegans male is controlled by the temporally regulated miRNA let-7 and its target lin-41, a translational regulator. lin-41 acts through lin-29a, an isoform of a conserved Zn finger transcription factor, expressed in a subset of sex-shared neurons only in the male. Ectopic lin-29a is sufficient to impose male-specific features at earlier stages of development and in the opposite sex. The temporal, sexual and spatial specificity of lin-29a expression is controlled intersectionally through the lin-28/let-7/lin-41 heterochronic pathway, sex chromosome configuration and neuron-type-specific terminal selector transcription factors. Two Doublesex-like transcription factors represent additional sex- and neuron-type specific targets of LIN-41 and are regulated in a similar intersectional manner.
Keyphrases
  • transcription factor
  • dna binding
  • mental health
  • spinal cord
  • spinal cord injury
  • dna methylation
  • heavy metals
  • gene expression
  • mass spectrometry
  • genome wide
  • blood brain barrier