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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |