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The Evolution of Human Cells in Terms of Protein Innovation

Humans are composed of hundreds of cell types. As the genomic DNA of each somatic cell is identical, cell type is determined by what is expressed and when. Until recently, little has been reported about the determinants of human cell identity, particularly from the joint perspective of gene evolutio...

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Autores principales: Sardar, Adam J., Oates, Matt E., Fang, Hai, Forrest, Alistair R.R., Kawaji, Hideya, Gough, Julian, Rackham, Owen J.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032124/
https://www.ncbi.nlm.nih.gov/pubmed/24692656
http://dx.doi.org/10.1093/molbev/mst139
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author Sardar, Adam J.
Oates, Matt E.
Fang, Hai
Forrest, Alistair R.R.
Kawaji, Hideya
Gough, Julian
Rackham, Owen J.L.
author_facet Sardar, Adam J.
Oates, Matt E.
Fang, Hai
Forrest, Alistair R.R.
Kawaji, Hideya
Gough, Julian
Rackham, Owen J.L.
author_sort Sardar, Adam J.
collection PubMed
description Humans are composed of hundreds of cell types. As the genomic DNA of each somatic cell is identical, cell type is determined by what is expressed and when. Until recently, little has been reported about the determinants of human cell identity, particularly from the joint perspective of gene evolution and expression. Here, we chart the evolutionary past of all documented human cell types via the collective histories of proteins, the principal product of gene expression. FANTOM5 data provide cell-type–specific digital expression of human protein-coding genes and the SUPERFAMILY resource is used to provide protein domain annotation. The evolutionary epoch in which each protein was created is inferred by comparison with domain annotation of all other completely sequenced genomes. Studying the distribution across epochs of genes expressed in each cell type reveals insights into human cellular evolution in terms of protein innovation. For each cell type, its history of protein innovation is charted based on the genes it expresses. Combining the histories of all cell types enables us to create a timeline of cell evolution. This timeline identifies the possibility that our common ancestor Coelomata (cavity-forming animals) provided the innovation required for the innate immune system, whereas cells which now form the brain of human have followed a trajectory of continually accumulating novel proteins since Opisthokonta (boundary of animals and fungi). We conclude that exaptation of existing domain architectures into new contexts is the dominant source of cell-type–specific domain architectures.
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spelling pubmed-40321242014-06-18 The Evolution of Human Cells in Terms of Protein Innovation Sardar, Adam J. Oates, Matt E. Fang, Hai Forrest, Alistair R.R. Kawaji, Hideya Gough, Julian Rackham, Owen J.L. Mol Biol Evol Discoveries Humans are composed of hundreds of cell types. As the genomic DNA of each somatic cell is identical, cell type is determined by what is expressed and when. Until recently, little has been reported about the determinants of human cell identity, particularly from the joint perspective of gene evolution and expression. Here, we chart the evolutionary past of all documented human cell types via the collective histories of proteins, the principal product of gene expression. FANTOM5 data provide cell-type–specific digital expression of human protein-coding genes and the SUPERFAMILY resource is used to provide protein domain annotation. The evolutionary epoch in which each protein was created is inferred by comparison with domain annotation of all other completely sequenced genomes. Studying the distribution across epochs of genes expressed in each cell type reveals insights into human cellular evolution in terms of protein innovation. For each cell type, its history of protein innovation is charted based on the genes it expresses. Combining the histories of all cell types enables us to create a timeline of cell evolution. This timeline identifies the possibility that our common ancestor Coelomata (cavity-forming animals) provided the innovation required for the innate immune system, whereas cells which now form the brain of human have followed a trajectory of continually accumulating novel proteins since Opisthokonta (boundary of animals and fungi). We conclude that exaptation of existing domain architectures into new contexts is the dominant source of cell-type–specific domain architectures. Oxford University Press 2014-06 2014-03-29 /pmc/articles/PMC4032124/ /pubmed/24692656 http://dx.doi.org/10.1093/molbev/mst139 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), 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 Discoveries
Sardar, Adam J.
Oates, Matt E.
Fang, Hai
Forrest, Alistair R.R.
Kawaji, Hideya
Gough, Julian
Rackham, Owen J.L.
The Evolution of Human Cells in Terms of Protein Innovation
title The Evolution of Human Cells in Terms of Protein Innovation
title_full The Evolution of Human Cells in Terms of Protein Innovation
title_fullStr The Evolution of Human Cells in Terms of Protein Innovation
title_full_unstemmed The Evolution of Human Cells in Terms of Protein Innovation
title_short The Evolution of Human Cells in Terms of Protein Innovation
title_sort evolution of human cells in terms of protein innovation
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032124/
https://www.ncbi.nlm.nih.gov/pubmed/24692656
http://dx.doi.org/10.1093/molbev/mst139
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