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

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 func...

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Main Authors: 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
Format: Article
Language:English
Published: Elsevier 2016-04-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S221112471630290X
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author 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
author_facet 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
author_sort Mitchell D’Rozario
collection DOAJ
description 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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spelling doaj.art-030c7014471548abaa2e6ab34c59e9db2022-12-22T02:03:45ZengElsevierCell Reports2211-12472016-04-0115238639710.1016/j.celrep.2016.03.034Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic NeuronsMitchell D’Rozario0Ting Zhang1Edward A. Waddell2Yonggang Zhang3Cem Sahin4Michal Sharoni5Tina Hu6Mohammad Nayal7Kaveesh Kutty8Faith Liebl9Wenhui Hu10Daniel R. Marenda11Department of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USADepartment of Electrical and Computer Engineering, Drexel University, Philadelphia, PA 19104, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USADepartment of Biological Sciences, Southern Illinois University Edwardsville, Edwardsville, IL 62026, USADepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USADepartment of Biology, Drexel University, Philadelphia, PA 19104, USAProneural 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.http://www.sciencedirect.com/science/article/pii/S221112471630290XdaughterlessTCF4NMJproneuralbHLHPitt-Hopkinsschizophrenia
spellingShingle 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
Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
Cell Reports
daughterless
TCF4
NMJ
proneural
bHLH
Pitt-Hopkins
schizophrenia
title Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
title_full Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
title_fullStr Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
title_full_unstemmed Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
title_short Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons
title_sort type i bhlh proteins daughterless and tcf4 restrict neurite branching and synapse formation by repressing neurexin in postmitotic neurons
topic daughterless
TCF4
NMJ
proneural
bHLH
Pitt-Hopkins
schizophrenia
url http://www.sciencedirect.com/science/article/pii/S221112471630290X
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