Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.

In most animal species, males and females exhibit differences in behavior and morphology that relate to their respective roles in reproduction. DM (Doublesex/MAB-3) domain transcription factors are phylogenetically conserved regulators of sexual development. They are thought to establish sexual trai...

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Main Authors: Meagan S Siehr, Pamela K Koo, Amrita L Sherlekar, Xuelin Bian, Meredith R Bunkers, Renee M Miller, Douglas S Portman, Robyn Lints
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3206049?pdf=render
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author Meagan S Siehr
Pamela K Koo
Amrita L Sherlekar
Xuelin Bian
Meredith R Bunkers
Renee M Miller
Douglas S Portman
Robyn Lints
author_facet Meagan S Siehr
Pamela K Koo
Amrita L Sherlekar
Xuelin Bian
Meredith R Bunkers
Renee M Miller
Douglas S Portman
Robyn Lints
author_sort Meagan S Siehr
collection DOAJ
description In most animal species, males and females exhibit differences in behavior and morphology that relate to their respective roles in reproduction. DM (Doublesex/MAB-3) domain transcription factors are phylogenetically conserved regulators of sexual development. They are thought to establish sexual traits by sex-specifically modifying the activity of general developmental programs. However, there are few examples where the details of these interactions are known, particularly in the nervous system.In this study, we show that two C. elegans DM domain genes, dmd-3 and mab-23, regulate sensory and muscle cell development in a male neural circuit required for mating. Using genetic approaches, we show that in the circuit sensory neurons, dmd-3 and mab-23 establish the correct pattern of dopaminergic (DA) and cholinergic (ACh) fate. We find that the ETS-domain transcription factor gene ast-1, a non-sex-specific, phylogenetically conserved activator of dopamine biosynthesis gene transcription, is broadly expressed in the circuit sensory neuron population. However, dmd-3 and mab-23 repress its activity in most cells, promoting ACh fate instead. A subset of neurons, preferentially exposed to a TGF-beta ligand, escape this repression because signal transduction pathway activity in these cells blocks dmd-3/mab-23 function, allowing DA fate to be established. Through optogenetic and pharmacological approaches, we show that the sensory and muscle cell characteristics controlled by dmd-3 and mab-23 are crucial for circuit function.In the C. elegans male, DM domain genes dmd-3 and mab-23 regulate expression of cell sub-type characteristics that are critical for mating success. In particular, these factors limit the number of DA neurons in the male nervous system by sex-specifically regulating a phylogenetically conserved dopamine biosynthesis gene transcription factor. Homologous interactions between vertebrate counterparts could regulate sex differences in neuron sub-type populations in the brain.
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spelling doaj.art-999a1d8745a04c00b3be79713886f4c12022-12-22T01:15:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01611e2681110.1371/journal.pone.0026811Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.Meagan S SiehrPamela K KooAmrita L SherlekarXuelin BianMeredith R BunkersRenee M MillerDouglas S PortmanRobyn LintsIn most animal species, males and females exhibit differences in behavior and morphology that relate to their respective roles in reproduction. DM (Doublesex/MAB-3) domain transcription factors are phylogenetically conserved regulators of sexual development. They are thought to establish sexual traits by sex-specifically modifying the activity of general developmental programs. However, there are few examples where the details of these interactions are known, particularly in the nervous system.In this study, we show that two C. elegans DM domain genes, dmd-3 and mab-23, regulate sensory and muscle cell development in a male neural circuit required for mating. Using genetic approaches, we show that in the circuit sensory neurons, dmd-3 and mab-23 establish the correct pattern of dopaminergic (DA) and cholinergic (ACh) fate. We find that the ETS-domain transcription factor gene ast-1, a non-sex-specific, phylogenetically conserved activator of dopamine biosynthesis gene transcription, is broadly expressed in the circuit sensory neuron population. However, dmd-3 and mab-23 repress its activity in most cells, promoting ACh fate instead. A subset of neurons, preferentially exposed to a TGF-beta ligand, escape this repression because signal transduction pathway activity in these cells blocks dmd-3/mab-23 function, allowing DA fate to be established. Through optogenetic and pharmacological approaches, we show that the sensory and muscle cell characteristics controlled by dmd-3 and mab-23 are crucial for circuit function.In the C. elegans male, DM domain genes dmd-3 and mab-23 regulate expression of cell sub-type characteristics that are critical for mating success. In particular, these factors limit the number of DA neurons in the male nervous system by sex-specifically regulating a phylogenetically conserved dopamine biosynthesis gene transcription factor. Homologous interactions between vertebrate counterparts could regulate sex differences in neuron sub-type populations in the brain.http://europepmc.org/articles/PMC3206049?pdf=render
spellingShingle Meagan S Siehr
Pamela K Koo
Amrita L Sherlekar
Xuelin Bian
Meredith R Bunkers
Renee M Miller
Douglas S Portman
Robyn Lints
Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
PLoS ONE
title Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
title_full Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
title_fullStr Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
title_full_unstemmed Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
title_short Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit.
title_sort multiple doublesex related genes specify critical cell fates in a c elegans male neural circuit
url http://europepmc.org/articles/PMC3206049?pdf=render
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