AI Article Synopsis

  • * Bhlhb5 forms a repressor complex with Prdm8, which binds to specific DNA sequences to suppress target genes, a function critical for proper neuronal behavior and cellular organization.
  • * Mice lacking either Bhlhb5 or Prdm8 exhibit similar developmental issues, underscoring their partnership in regulating Cadherin-11 to ensure correct neural circuit formation.

Article Abstract

Although transcription factors that repress gene expression play critical roles in nervous system development, their mechanism of action remains to be understood. Here, we report that the Olig-related transcription factor Bhlhb5 (also known as Bhlhe22) forms a repressor complex with the PR/SET domain protein, Prdm8. We find that Bhlhb5 binds to sequence-specific DNA elements and then recruits Prdm8, which mediates the repression of target genes. This interaction is critical for repressor function since mice lacking either Bhlhb5 or Prdm8 have strikingly similar cellular and behavioral phenotypes, including axonal mistargeting by neurons of the dorsal telencephalon and abnormal itch-like behavior. We provide evidence that Cadherin-11 functions as target of the Prdm8/Bhlhb5 repressor complex that must be repressed for proper neural circuit formation to occur. These findings suggest that Prdm8 is an obligate partner of Bhlhb5, forming a repressor complex that directs neural circuit assembly in part through the precise regulation of Cadherin-11.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269007PMC
http://dx.doi.org/10.1016/j.neuron.2011.09.035DOI Listing

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