Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons

型 bHLH 蛋白 Daughterless 和 Tcf4 通过抑制有丝分裂后神经元中的 Neuroxin 来限制神经突分支和突触形成

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作者:Mitchell D'Rozario, Ting Zhang, Edward A Waddell, Yonggang Zhang, Cem Sahin, Michal Sharoni, Tina Hu, Mohammad Nayal, Kaveesh Kutty, Faith Liebl, Wenhui Hu, Daniel R Marenda

Abstract

Proneural proteins of the class I/II basic-helix-loop-helix (bHLH) family are highly conserved transcription factors. Class I bHLH proteins are expressed in a broad number of tissues during development, whereas class II bHLH protein expression is more tissue restricted. Our understanding of the function of class I/II bHLH transcription factors in both invertebrate and vertebrate neurobiology is largely focused on their function as regulators of neurogenesis. Here, we show that the class I bHLH proteins Daughterless and Tcf4 are expressed in postmitotic neurons in Drosophila melanogaster and mice, respectively, where they function to restrict neurite branching and synapse formation. Our data indicate that Daughterless performs this function in part by restricting the expression of the cell adhesion molecule Neurexin. This suggests a role for these proteins outside of their established roles in neurogenesis.

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