Cargando…

In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system

The generation of the enormous diversity of neuronal cell types in a differentiating nervous system entails the activation of neuron type-specific gene batteries. To examine the regulatory logic that controls the expression of neuron type-specific gene batteries, we interrogate single cell expressio...

Descripción completa

Detalles Bibliográficos
Autores principales: Glenwinkel, Lori, Taylor, Seth R, Langebeck-Jensen, Kasper, Pereira, Laura, Reilly, Molly B, Basavaraju, Manasa, Rafi, Ibnul, Yemini, Eviatar, Pocock, Roger, Sestan, Nenad, Hammarlund, Marc, Miller, David M, Hobert, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225391/
https://www.ncbi.nlm.nih.gov/pubmed/34165430
http://dx.doi.org/10.7554/eLife.64906
_version_ 1783712080572973056
author Glenwinkel, Lori
Taylor, Seth R
Langebeck-Jensen, Kasper
Pereira, Laura
Reilly, Molly B
Basavaraju, Manasa
Rafi, Ibnul
Yemini, Eviatar
Pocock, Roger
Sestan, Nenad
Hammarlund, Marc
Miller, David M
Hobert, Oliver
author_facet Glenwinkel, Lori
Taylor, Seth R
Langebeck-Jensen, Kasper
Pereira, Laura
Reilly, Molly B
Basavaraju, Manasa
Rafi, Ibnul
Yemini, Eviatar
Pocock, Roger
Sestan, Nenad
Hammarlund, Marc
Miller, David M
Hobert, Oliver
author_sort Glenwinkel, Lori
collection PubMed
description The generation of the enormous diversity of neuronal cell types in a differentiating nervous system entails the activation of neuron type-specific gene batteries. To examine the regulatory logic that controls the expression of neuron type-specific gene batteries, we interrogate single cell expression profiles of all 118 neuron classes of the Caenorhabditis elegans nervous system for the presence of DNA binding motifs of 136 neuronally expressed C. elegans transcription factors. Using a phylogenetic footprinting pipeline, we identify cis-regulatory motif enrichments among neuron class-specific gene batteries and we identify cognate transcription factors for 117 of the 118 neuron classes. In addition to predicting novel regulators of neuronal identities, our nervous system-wide analysis at single cell resolution supports the hypothesis that many transcription factors directly co-regulate the cohort of effector genes that define a neuron type, thereby corroborating the concept of so-called terminal selectors of neuronal identity. Our analysis provides a blueprint for how individual components of an entire nervous system are genetically specified.
format Online
Article
Text
id pubmed-8225391
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-82253912021-06-28 In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system Glenwinkel, Lori Taylor, Seth R Langebeck-Jensen, Kasper Pereira, Laura Reilly, Molly B Basavaraju, Manasa Rafi, Ibnul Yemini, Eviatar Pocock, Roger Sestan, Nenad Hammarlund, Marc Miller, David M Hobert, Oliver eLife Neuroscience The generation of the enormous diversity of neuronal cell types in a differentiating nervous system entails the activation of neuron type-specific gene batteries. To examine the regulatory logic that controls the expression of neuron type-specific gene batteries, we interrogate single cell expression profiles of all 118 neuron classes of the Caenorhabditis elegans nervous system for the presence of DNA binding motifs of 136 neuronally expressed C. elegans transcription factors. Using a phylogenetic footprinting pipeline, we identify cis-regulatory motif enrichments among neuron class-specific gene batteries and we identify cognate transcription factors for 117 of the 118 neuron classes. In addition to predicting novel regulators of neuronal identities, our nervous system-wide analysis at single cell resolution supports the hypothesis that many transcription factors directly co-regulate the cohort of effector genes that define a neuron type, thereby corroborating the concept of so-called terminal selectors of neuronal identity. Our analysis provides a blueprint for how individual components of an entire nervous system are genetically specified. eLife Sciences Publications, Ltd 2021-06-24 /pmc/articles/PMC8225391/ /pubmed/34165430 http://dx.doi.org/10.7554/eLife.64906 Text en © 2021, Glenwinkel et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Glenwinkel, Lori
Taylor, Seth R
Langebeck-Jensen, Kasper
Pereira, Laura
Reilly, Molly B
Basavaraju, Manasa
Rafi, Ibnul
Yemini, Eviatar
Pocock, Roger
Sestan, Nenad
Hammarlund, Marc
Miller, David M
Hobert, Oliver
In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title_full In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title_fullStr In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title_full_unstemmed In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title_short In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system
title_sort in silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the c. elegans nervous system
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225391/
https://www.ncbi.nlm.nih.gov/pubmed/34165430
http://dx.doi.org/10.7554/eLife.64906
work_keys_str_mv AT glenwinkellori insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT taylorsethr insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT langebeckjensenkasper insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT pereiralaura insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT reillymollyb insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT basavarajumanasa insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT rafiibnul insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT yeminieviatar insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT pocockroger insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT sestannenad insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT hammarlundmarc insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT millerdavidm insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem
AT hobertoliver insilicoanalysisofthetranscriptionalregulatorylogicofneuronalidentityspecificationthroughoutthecelegansnervoussystem