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Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis

The success of marker-based approaches for dissecting haematopoiesis in mouse and human is reliant on the presence of well-defined cell surface markers specific for diverse progenitor populations. An inherent problem with this approach is that the presence of specific cell surface markers does not d...

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Autores principales: Athanasiadis, Emmanouil I., Botthof, Jan G., Andres, Helena, Ferreira, Lauren, Lio, Pietro, Cvejic, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725498/
https://www.ncbi.nlm.nih.gov/pubmed/29229905
http://dx.doi.org/10.1038/s41467-017-02305-6
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author Athanasiadis, Emmanouil I.
Botthof, Jan G.
Andres, Helena
Ferreira, Lauren
Lio, Pietro
Cvejic, Ana
author_facet Athanasiadis, Emmanouil I.
Botthof, Jan G.
Andres, Helena
Ferreira, Lauren
Lio, Pietro
Cvejic, Ana
author_sort Athanasiadis, Emmanouil I.
collection PubMed
description The success of marker-based approaches for dissecting haematopoiesis in mouse and human is reliant on the presence of well-defined cell surface markers specific for diverse progenitor populations. An inherent problem with this approach is that the presence of specific cell surface markers does not directly reflect the transcriptional state of a cell. Here, we used a marker-free approach to computationally reconstruct the blood lineage tree in zebrafish and order cells along their differentiation trajectory, based on their global transcriptional differences. Within the population of transcriptionally similar stem and progenitor cells, our analysis reveals considerable cell-to-cell differences in their probability to transition to another committed state. Once fate decision is executed, the suppression of transcription of ribosomal genes and upregulation of lineage-specific factors coordinately controls lineage differentiation. Evolutionary analysis further demonstrates that this haematopoietic programme is highly conserved between zebrafish and higher vertebrates.
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spelling pubmed-57254982017-12-14 Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis Athanasiadis, Emmanouil I. Botthof, Jan G. Andres, Helena Ferreira, Lauren Lio, Pietro Cvejic, Ana Nat Commun Article The success of marker-based approaches for dissecting haematopoiesis in mouse and human is reliant on the presence of well-defined cell surface markers specific for diverse progenitor populations. An inherent problem with this approach is that the presence of specific cell surface markers does not directly reflect the transcriptional state of a cell. Here, we used a marker-free approach to computationally reconstruct the blood lineage tree in zebrafish and order cells along their differentiation trajectory, based on their global transcriptional differences. Within the population of transcriptionally similar stem and progenitor cells, our analysis reveals considerable cell-to-cell differences in their probability to transition to another committed state. Once fate decision is executed, the suppression of transcription of ribosomal genes and upregulation of lineage-specific factors coordinately controls lineage differentiation. Evolutionary analysis further demonstrates that this haematopoietic programme is highly conserved between zebrafish and higher vertebrates. Nature Publishing Group UK 2017-12-11 /pmc/articles/PMC5725498/ /pubmed/29229905 http://dx.doi.org/10.1038/s41467-017-02305-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Athanasiadis, Emmanouil I.
Botthof, Jan G.
Andres, Helena
Ferreira, Lauren
Lio, Pietro
Cvejic, Ana
Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title_full Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title_fullStr Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title_full_unstemmed Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title_short Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
title_sort single-cell rna-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725498/
https://www.ncbi.nlm.nih.gov/pubmed/29229905
http://dx.doi.org/10.1038/s41467-017-02305-6
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