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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-4032124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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