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Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior
Sex-specific synaptic connectivity is beginning to emerge as a remarkable, but little explored feature of animal brains. We describe here a novel mechanism that promotes sexually dimorphic neuronal function and synaptic connectivity in the nervous system of the nematode Caenorhabditis elegans. We de...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538159/ https://www.ncbi.nlm.nih.gov/pubmed/33021200 http://dx.doi.org/10.7554/eLife.59614 |
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author | Bayer, Emily A Stecky, Rebecca C Neal, Lauren Katsamba, Phinikoula S Ahlsen, Goran Balaji, Vishnu Hoppe, Thorsten Shapiro, Lawrence Oren-Suissa, Meital Hobert, Oliver |
author_facet | Bayer, Emily A Stecky, Rebecca C Neal, Lauren Katsamba, Phinikoula S Ahlsen, Goran Balaji, Vishnu Hoppe, Thorsten Shapiro, Lawrence Oren-Suissa, Meital Hobert, Oliver |
author_sort | Bayer, Emily A |
collection | PubMed |
description | Sex-specific synaptic connectivity is beginning to emerge as a remarkable, but little explored feature of animal brains. We describe here a novel mechanism that promotes sexually dimorphic neuronal function and synaptic connectivity in the nervous system of the nematode Caenorhabditis elegans. We demonstrate that a phylogenetically conserved, but previously uncharacterized Doublesex/Mab-3 related transcription factor (DMRT), dmd-4, is expressed in two classes of sex-shared phasmid neurons specifically in hermaphrodites but not in males. We find dmd-4 to promote hermaphrodite-specific synaptic connectivity and neuronal function of phasmid sensory neurons. Sex-specificity of DMD-4 function is conferred by a novel mode of posttranslational regulation that involves sex-specific protein stabilization through ubiquitin binding to a phylogenetically conserved but previously unstudied protein domain, the DMA domain. A human DMRT homolog of DMD-4 is controlled in a similar manner, indicating that our findings may have implications for the control of sexual differentiation in other animals as well. |
format | Online Article Text |
id | pubmed-7538159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75381592020-10-07 Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior Bayer, Emily A Stecky, Rebecca C Neal, Lauren Katsamba, Phinikoula S Ahlsen, Goran Balaji, Vishnu Hoppe, Thorsten Shapiro, Lawrence Oren-Suissa, Meital Hobert, Oliver eLife Neuroscience Sex-specific synaptic connectivity is beginning to emerge as a remarkable, but little explored feature of animal brains. We describe here a novel mechanism that promotes sexually dimorphic neuronal function and synaptic connectivity in the nervous system of the nematode Caenorhabditis elegans. We demonstrate that a phylogenetically conserved, but previously uncharacterized Doublesex/Mab-3 related transcription factor (DMRT), dmd-4, is expressed in two classes of sex-shared phasmid neurons specifically in hermaphrodites but not in males. We find dmd-4 to promote hermaphrodite-specific synaptic connectivity and neuronal function of phasmid sensory neurons. Sex-specificity of DMD-4 function is conferred by a novel mode of posttranslational regulation that involves sex-specific protein stabilization through ubiquitin binding to a phylogenetically conserved but previously unstudied protein domain, the DMA domain. A human DMRT homolog of DMD-4 is controlled in a similar manner, indicating that our findings may have implications for the control of sexual differentiation in other animals as well. eLife Sciences Publications, Ltd 2020-10-06 /pmc/articles/PMC7538159/ /pubmed/33021200 http://dx.doi.org/10.7554/eLife.59614 Text en © 2020, Bayer et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Bayer, Emily A Stecky, Rebecca C Neal, Lauren Katsamba, Phinikoula S Ahlsen, Goran Balaji, Vishnu Hoppe, Thorsten Shapiro, Lawrence Oren-Suissa, Meital Hobert, Oliver Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title_full | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title_fullStr | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title_full_unstemmed | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title_short | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
title_sort | ubiquitin-dependent regulation of a conserved dmrt protein controls sexually dimorphic synaptic connectivity and behavior |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538159/ https://www.ncbi.nlm.nih.gov/pubmed/33021200 http://dx.doi.org/10.7554/eLife.59614 |
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