| Literature DB >> 27050508 |
Mitchell D'Rozario1, Ting Zhang2, Edward A Waddell1, Yonggang Zhang2, Cem Sahin3, Michal Sharoni1, Tina Hu1, Mohammad Nayal1, Kaveesh Kutty1, Faith Liebl4, Wenhui Hu5, Daniel R Marenda6.
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.Entities:
Keywords: NMJ; Pitt-Hopkins; TCF4; bHLH; daughterless; proneural; schizophrenia
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Year: 2016 PMID: 27050508 PMCID: PMC4946342 DOI: 10.1016/j.celrep.2016.03.034
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423