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Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body

Animal bodies comprise diverse arrays of cells. To characterize cellular identities across an entire body, we have compared the transcriptomes of single cells randomly picked from dissociated whole larvae of the marine annelid Platynereis dumerilii. We identify five transcriptionally distinct groups...

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Autores principales: Achim, Kaia, Eling, Nils, Vergara, Hernando Martinez, Bertucci, Paola Yanina, Musser, Jacob, Vopalensky, Pavel, Brunet, Thibaut, Collier, Paul, Benes, Vladimir, Marioni, John C, Arendt, Detlev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913682/
https://www.ncbi.nlm.nih.gov/pubmed/29373712
http://dx.doi.org/10.1093/molbev/msx336
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author Achim, Kaia
Eling, Nils
Vergara, Hernando Martinez
Bertucci, Paola Yanina
Musser, Jacob
Vopalensky, Pavel
Brunet, Thibaut
Collier, Paul
Benes, Vladimir
Marioni, John C
Arendt, Detlev
author_facet Achim, Kaia
Eling, Nils
Vergara, Hernando Martinez
Bertucci, Paola Yanina
Musser, Jacob
Vopalensky, Pavel
Brunet, Thibaut
Collier, Paul
Benes, Vladimir
Marioni, John C
Arendt, Detlev
author_sort Achim, Kaia
collection PubMed
description Animal bodies comprise diverse arrays of cells. To characterize cellular identities across an entire body, we have compared the transcriptomes of single cells randomly picked from dissociated whole larvae of the marine annelid Platynereis dumerilii. We identify five transcriptionally distinct groups of differentiated cells, each expressing a unique set of transcription factors and effector genes that implement cellular phenotypes. Spatial mapping of cells into a cellular expression atlas, and wholemount in situ hybridization of group-specific genes reveals spatially coherent transcriptional domains in the larval body, comprising, for example, apical sensory-neurosecretory cells versus neural/epidermal surface cells. These domains represent new, basic subdivisions of the annelid body based entirely on differential gene expression, and are composed of multiple, transcriptionally similar cell types. They do not represent clonal domains, as revealed by developmental lineage analysis. We propose that the transcriptional domains that subdivide the annelid larval body represent families of related cell types that have arisen by evolutionary diversification. Their possible evolutionary conservation makes them a promising tool for evo–devo research.
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spelling pubmed-59136822018-04-30 Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body Achim, Kaia Eling, Nils Vergara, Hernando Martinez Bertucci, Paola Yanina Musser, Jacob Vopalensky, Pavel Brunet, Thibaut Collier, Paul Benes, Vladimir Marioni, John C Arendt, Detlev Mol Biol Evol Fast Track Animal bodies comprise diverse arrays of cells. To characterize cellular identities across an entire body, we have compared the transcriptomes of single cells randomly picked from dissociated whole larvae of the marine annelid Platynereis dumerilii. We identify five transcriptionally distinct groups of differentiated cells, each expressing a unique set of transcription factors and effector genes that implement cellular phenotypes. Spatial mapping of cells into a cellular expression atlas, and wholemount in situ hybridization of group-specific genes reveals spatially coherent transcriptional domains in the larval body, comprising, for example, apical sensory-neurosecretory cells versus neural/epidermal surface cells. These domains represent new, basic subdivisions of the annelid body based entirely on differential gene expression, and are composed of multiple, transcriptionally similar cell types. They do not represent clonal domains, as revealed by developmental lineage analysis. We propose that the transcriptional domains that subdivide the annelid larval body represent families of related cell types that have arisen by evolutionary diversification. Their possible evolutionary conservation makes them a promising tool for evo–devo research. Oxford University Press 2018-05 2018-01-24 /pmc/articles/PMC5913682/ /pubmed/29373712 http://dx.doi.org/10.1093/molbev/msx336 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Fast Track
Achim, Kaia
Eling, Nils
Vergara, Hernando Martinez
Bertucci, Paola Yanina
Musser, Jacob
Vopalensky, Pavel
Brunet, Thibaut
Collier, Paul
Benes, Vladimir
Marioni, John C
Arendt, Detlev
Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title_full Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title_fullStr Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title_full_unstemmed Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title_short Whole-Body Single-Cell Sequencing Reveals Transcriptional Domains in the Annelid Larval Body
title_sort whole-body single-cell sequencing reveals transcriptional domains in the annelid larval body
topic Fast Track
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913682/
https://www.ncbi.nlm.nih.gov/pubmed/29373712
http://dx.doi.org/10.1093/molbev/msx336
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