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