Cargando…

A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs

Cell type specification during early nervous system development in Drosophila melanogaster requires precise regulation of gene expression in time and space. Resolving the programs driving neurogenesis has been a major challenge owing to the complexity and rapidity with which distinct cell population...

Descripción completa

Detalles Bibliográficos
Autores principales: McCorkindale, Alexandra L., Wahle, Philipp, Werner, Sascha, Jungreis, Irwin, Menzel, Peter, Shukla, Chinmay J., Abreu, Rúben Lopes Pereira, Irizarry, Rafael A., Meyer, Irmtraud M., Kellis, Manolis, Zinzen, Robert P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451322/
https://www.ncbi.nlm.nih.gov/pubmed/30923056
http://dx.doi.org/10.1242/dev.175265
_version_ 1783409175941873664
author McCorkindale, Alexandra L.
Wahle, Philipp
Werner, Sascha
Jungreis, Irwin
Menzel, Peter
Shukla, Chinmay J.
Abreu, Rúben Lopes Pereira
Irizarry, Rafael A.
Meyer, Irmtraud M.
Kellis, Manolis
Zinzen, Robert P.
author_facet McCorkindale, Alexandra L.
Wahle, Philipp
Werner, Sascha
Jungreis, Irwin
Menzel, Peter
Shukla, Chinmay J.
Abreu, Rúben Lopes Pereira
Irizarry, Rafael A.
Meyer, Irmtraud M.
Kellis, Manolis
Zinzen, Robert P.
author_sort McCorkindale, Alexandra L.
collection PubMed
description Cell type specification during early nervous system development in Drosophila melanogaster requires precise regulation of gene expression in time and space. Resolving the programs driving neurogenesis has been a major challenge owing to the complexity and rapidity with which distinct cell populations arise. To resolve the cell type-specific gene expression dynamics in early nervous system development, we have sequenced the transcriptomes of purified neurogenic cell types across consecutive time points covering crucial events in neurogenesis. The resulting gene expression atlas comprises a detailed resource of global transcriptome dynamics that permits systematic analysis of how cells in the nervous system acquire distinct fates. We resolve known gene expression dynamics and uncover novel expression signatures for hundreds of genes among diverse neurogenic cell types, most of which remain unstudied. We also identified a set of conserved long noncoding RNAs (lncRNAs) that are regulated in a tissue-specific manner and exhibit spatiotemporal expression during neurogenesis with exquisite specificity. lncRNA expression is highly dynamic and demarcates specific subpopulations within neurogenic cell types. Our spatiotemporal transcriptome atlas provides a comprehensive resource for investigating the function of coding genes and noncoding RNAs during crucial stages of early neurogenesis.
format Online
Article
Text
id pubmed-6451322
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-64513222019-04-25 A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs McCorkindale, Alexandra L. Wahle, Philipp Werner, Sascha Jungreis, Irwin Menzel, Peter Shukla, Chinmay J. Abreu, Rúben Lopes Pereira Irizarry, Rafael A. Meyer, Irmtraud M. Kellis, Manolis Zinzen, Robert P. Development Techniques and Resources Cell type specification during early nervous system development in Drosophila melanogaster requires precise regulation of gene expression in time and space. Resolving the programs driving neurogenesis has been a major challenge owing to the complexity and rapidity with which distinct cell populations arise. To resolve the cell type-specific gene expression dynamics in early nervous system development, we have sequenced the transcriptomes of purified neurogenic cell types across consecutive time points covering crucial events in neurogenesis. The resulting gene expression atlas comprises a detailed resource of global transcriptome dynamics that permits systematic analysis of how cells in the nervous system acquire distinct fates. We resolve known gene expression dynamics and uncover novel expression signatures for hundreds of genes among diverse neurogenic cell types, most of which remain unstudied. We also identified a set of conserved long noncoding RNAs (lncRNAs) that are regulated in a tissue-specific manner and exhibit spatiotemporal expression during neurogenesis with exquisite specificity. lncRNA expression is highly dynamic and demarcates specific subpopulations within neurogenic cell types. Our spatiotemporal transcriptome atlas provides a comprehensive resource for investigating the function of coding genes and noncoding RNAs during crucial stages of early neurogenesis. The Company of Biologists Ltd 2019-03-15 2019-03-28 /pmc/articles/PMC6451322/ /pubmed/30923056 http://dx.doi.org/10.1242/dev.175265 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Techniques and Resources
McCorkindale, Alexandra L.
Wahle, Philipp
Werner, Sascha
Jungreis, Irwin
Menzel, Peter
Shukla, Chinmay J.
Abreu, Rúben Lopes Pereira
Irizarry, Rafael A.
Meyer, Irmtraud M.
Kellis, Manolis
Zinzen, Robert P.
A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title_full A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title_fullStr A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title_full_unstemmed A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title_short A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs
title_sort gene expression atlas of embryonic neurogenesis in drosophila reveals complex spatiotemporal regulation of lncrnas
topic Techniques and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451322/
https://www.ncbi.nlm.nih.gov/pubmed/30923056
http://dx.doi.org/10.1242/dev.175265
work_keys_str_mv AT mccorkindalealexandral ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT wahlephilipp ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT wernersascha ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT jungreisirwin ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT menzelpeter ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT shuklachinmayj ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT abreurubenlopespereira ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT irizarryrafaela ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT meyerirmtraudm ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT kellismanolis ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT zinzenrobertp ageneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT mccorkindalealexandral geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT wahlephilipp geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT wernersascha geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT jungreisirwin geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT menzelpeter geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT shuklachinmayj geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT abreurubenlopespereira geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT irizarryrafaela geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT meyerirmtraudm geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT kellismanolis geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas
AT zinzenrobertp geneexpressionatlasofembryonicneurogenesisindrosophilarevealscomplexspatiotemporalregulationoflncrnas