Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783316584238940160 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5913682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT achimkaia wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT elingnils wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT vergarahernandomartinez wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT bertuccipaolayanina wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT musserjacob wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT vopalenskypavel wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT brunetthibaut wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT collierpaul wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT benesvladimir wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT marionijohnc wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody AT arendtdetlev wholebodysinglecellsequencingrevealstranscriptionaldomainsintheannelidlarvalbody |