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Evolution of Neuronal and Endothelial Transcriptomes in Primates
The study of gene expression evolution in vertebrates has hitherto focused on the analysis of transcriptomes in tissues of different species. However, because a tissue is made up of different cell types, and cell types differ with respect to their transcriptomes, the analysis of tissues offers a com...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998193/ https://www.ncbi.nlm.nih.gov/pubmed/20624733 http://dx.doi.org/10.1093/gbe/evq018 |
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author | Giger, Thomas Khaitovich, Philipp Somel, Mehmet Lorenc, Anna Lizano, Esther Harris, Laura W. Ryan, Margaret M. Lan, Martin Wayland, Matthew T. Bahn, Sabine Pääbo, Svante |
author_facet | Giger, Thomas Khaitovich, Philipp Somel, Mehmet Lorenc, Anna Lizano, Esther Harris, Laura W. Ryan, Margaret M. Lan, Martin Wayland, Matthew T. Bahn, Sabine Pääbo, Svante |
author_sort | Giger, Thomas |
collection | PubMed |
description | The study of gene expression evolution in vertebrates has hitherto focused on the analysis of transcriptomes in tissues of different species. However, because a tissue is made up of different cell types, and cell types differ with respect to their transcriptomes, the analysis of tissues offers a composite picture of transcriptome evolution. The isolation of individual cells from tissue sections opens up the opportunity to study gene expression evolution at the cell type level. We have stained neurons and endothelial cells in human brains by antibodies against cell type-specific marker proteins, isolated the cells using laser capture microdissection, and identified genes preferentially expressed in the two cell types. We analyze these two classes of genes with respect to their expression in 62 different human tissues, with respect to their expression in 44 human “postmortem” brains from different developmental stages and with respect to between-species brain expression differences. We find that genes preferentially expressed in neurons differ less across tissues and developmental stages than genes preferentially expressed in endothelial cells. We also observe less expression differences within primate species for neuronal transcriptomes. In stark contrast, we see more gene expression differences between humans, chimpanzees, and rhesus macaques relative to within-species differences in genes expressed preferentially in neurons than in genes expressed in endothelial cells. This suggests that neuronal and endothelial transcriptomes evolve at different rates within brain tissue. |
format | Text |
id | pubmed-2998193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29981932010-12-07 Evolution of Neuronal and Endothelial Transcriptomes in Primates Giger, Thomas Khaitovich, Philipp Somel, Mehmet Lorenc, Anna Lizano, Esther Harris, Laura W. Ryan, Margaret M. Lan, Martin Wayland, Matthew T. Bahn, Sabine Pääbo, Svante Genome Biol Evol Letters The study of gene expression evolution in vertebrates has hitherto focused on the analysis of transcriptomes in tissues of different species. However, because a tissue is made up of different cell types, and cell types differ with respect to their transcriptomes, the analysis of tissues offers a composite picture of transcriptome evolution. The isolation of individual cells from tissue sections opens up the opportunity to study gene expression evolution at the cell type level. We have stained neurons and endothelial cells in human brains by antibodies against cell type-specific marker proteins, isolated the cells using laser capture microdissection, and identified genes preferentially expressed in the two cell types. We analyze these two classes of genes with respect to their expression in 62 different human tissues, with respect to their expression in 44 human “postmortem” brains from different developmental stages and with respect to between-species brain expression differences. We find that genes preferentially expressed in neurons differ less across tissues and developmental stages than genes preferentially expressed in endothelial cells. We also observe less expression differences within primate species for neuronal transcriptomes. In stark contrast, we see more gene expression differences between humans, chimpanzees, and rhesus macaques relative to within-species differences in genes expressed preferentially in neurons than in genes expressed in endothelial cells. This suggests that neuronal and endothelial transcriptomes evolve at different rates within brain tissue. Oxford University Press 2010 2010-05-07 /pmc/articles/PMC2998193/ /pubmed/20624733 http://dx.doi.org/10.1093/gbe/evq018 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Giger, Thomas Khaitovich, Philipp Somel, Mehmet Lorenc, Anna Lizano, Esther Harris, Laura W. Ryan, Margaret M. Lan, Martin Wayland, Matthew T. Bahn, Sabine Pääbo, Svante Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title | Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title_full | Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title_fullStr | Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title_full_unstemmed | Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title_short | Evolution of Neuronal and Endothelial Transcriptomes in Primates |
title_sort | evolution of neuronal and endothelial transcriptomes in primates |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998193/ https://www.ncbi.nlm.nih.gov/pubmed/20624733 http://dx.doi.org/10.1093/gbe/evq018 |
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