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Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling

Developmental neuronal remodeling is an evolutionarily conserved mechanism required for precise wiring of nervous systems. Despite its fundamental role in neurodevelopment and proposed contribution to various neuropsychiatric disorders, the underlying mechanisms are largely unknown. Here, we uncover...

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Autores principales: Alyagor, Idan, Berkun, Victoria, Keren-Shaul, Hadas, Marmor-Kollet, Neta, David, Eyal, Mayseless, Oded, Issman-Zecharya, Noa, Amit, Ido, Schuldiner, Oren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179959/
https://www.ncbi.nlm.nih.gov/pubmed/30300589
http://dx.doi.org/10.1016/j.devcel.2018.09.013
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author Alyagor, Idan
Berkun, Victoria
Keren-Shaul, Hadas
Marmor-Kollet, Neta
David, Eyal
Mayseless, Oded
Issman-Zecharya, Noa
Amit, Ido
Schuldiner, Oren
author_facet Alyagor, Idan
Berkun, Victoria
Keren-Shaul, Hadas
Marmor-Kollet, Neta
David, Eyal
Mayseless, Oded
Issman-Zecharya, Noa
Amit, Ido
Schuldiner, Oren
author_sort Alyagor, Idan
collection PubMed
description Developmental neuronal remodeling is an evolutionarily conserved mechanism required for precise wiring of nervous systems. Despite its fundamental role in neurodevelopment and proposed contribution to various neuropsychiatric disorders, the underlying mechanisms are largely unknown. Here, we uncover the fine temporal transcriptional landscape of Drosophila mushroom body γ neurons undergoing stereotypical remodeling. Our data reveal rapid and dramatic changes in the transcriptional landscape during development. Focusing on DNA binding proteins, we identify eleven that are required for remodeling. Furthermore, we sequence developing γ neurons perturbed for three key transcription factors required for pruning. We describe a hierarchical network featuring positive and negative feedback loops. Superimposing the perturbation-seq on the developmental expression atlas highlights a framework of transcriptional modules that together drive remodeling. Overall, this study provides a broad and detailed molecular insight into the complex regulatory dynamics of developmental remodeling and thus offers a pipeline to dissect developmental processes via RNA profiling.
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spelling pubmed-61799592018-10-12 Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling Alyagor, Idan Berkun, Victoria Keren-Shaul, Hadas Marmor-Kollet, Neta David, Eyal Mayseless, Oded Issman-Zecharya, Noa Amit, Ido Schuldiner, Oren Dev Cell Article Developmental neuronal remodeling is an evolutionarily conserved mechanism required for precise wiring of nervous systems. Despite its fundamental role in neurodevelopment and proposed contribution to various neuropsychiatric disorders, the underlying mechanisms are largely unknown. Here, we uncover the fine temporal transcriptional landscape of Drosophila mushroom body γ neurons undergoing stereotypical remodeling. Our data reveal rapid and dramatic changes in the transcriptional landscape during development. Focusing on DNA binding proteins, we identify eleven that are required for remodeling. Furthermore, we sequence developing γ neurons perturbed for three key transcription factors required for pruning. We describe a hierarchical network featuring positive and negative feedback loops. Superimposing the perturbation-seq on the developmental expression atlas highlights a framework of transcriptional modules that together drive remodeling. Overall, this study provides a broad and detailed molecular insight into the complex regulatory dynamics of developmental remodeling and thus offers a pipeline to dissect developmental processes via RNA profiling. Cell Press 2018-10-08 /pmc/articles/PMC6179959/ /pubmed/30300589 http://dx.doi.org/10.1016/j.devcel.2018.09.013 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Alyagor, Idan
Berkun, Victoria
Keren-Shaul, Hadas
Marmor-Kollet, Neta
David, Eyal
Mayseless, Oded
Issman-Zecharya, Noa
Amit, Ido
Schuldiner, Oren
Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title_full Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title_fullStr Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title_full_unstemmed Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title_short Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling
title_sort combining developmental and perturbation-seq uncovers transcriptional modules orchestrating neuronal remodeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179959/
https://www.ncbi.nlm.nih.gov/pubmed/30300589
http://dx.doi.org/10.1016/j.devcel.2018.09.013
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