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Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model
The evolution of complex skeletal traits in primates was likely influenced by both genetic and environmental factors. Because skeletal tissues are notoriously challenging to study using functional genomic approaches, they remain poorly characterized even in humans, let alone across multiple species....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936463/ https://www.ncbi.nlm.nih.gov/pubmed/35263340 http://dx.doi.org/10.1371/journal.pgen.1010073 |
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author | Housman, Genevieve Briscoe, Emilie Gilad, Yoav |
author_facet | Housman, Genevieve Briscoe, Emilie Gilad, Yoav |
author_sort | Housman, Genevieve |
collection | PubMed |
description | The evolution of complex skeletal traits in primates was likely influenced by both genetic and environmental factors. Because skeletal tissues are notoriously challenging to study using functional genomic approaches, they remain poorly characterized even in humans, let alone across multiple species. The challenges involved in obtaining functional genomic data from the skeleton, combined with the difficulty of obtaining such tissues from nonhuman apes, motivated us to consider an alternative in vitro system with which to comparatively study gene regulation in skeletal cell types. Specifically, we differentiated six human (Homo sapiens) and six chimpanzee (Pan troglodytes) induced pluripotent stem cell lines (iPSCs) into mesenchymal stem cells (MSCs) and subsequently into osteogenic cells (bone cells). We validated differentiation using standard methods and collected single-cell RNA sequencing data from over 100,000 cells across multiple samples and replicates at each stage of differentiation. While most genes that we examined display conserved patterns of expression across species, hundreds of genes are differentially expressed (DE) between humans and chimpanzees within and across stages of osteogenic differentiation. Some of these interspecific DE genes show functional enrichments relevant in skeletal tissue trait development. Moreover, topic modeling indicates that interspecific gene programs become more pronounced as cells mature. Overall, we propose that this in vitro model can be used to identify interspecific regulatory differences that may have contributed to skeletal trait differences between species. |
format | Online Article Text |
id | pubmed-8936463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89364632022-03-22 Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model Housman, Genevieve Briscoe, Emilie Gilad, Yoav PLoS Genet Research Article The evolution of complex skeletal traits in primates was likely influenced by both genetic and environmental factors. Because skeletal tissues are notoriously challenging to study using functional genomic approaches, they remain poorly characterized even in humans, let alone across multiple species. The challenges involved in obtaining functional genomic data from the skeleton, combined with the difficulty of obtaining such tissues from nonhuman apes, motivated us to consider an alternative in vitro system with which to comparatively study gene regulation in skeletal cell types. Specifically, we differentiated six human (Homo sapiens) and six chimpanzee (Pan troglodytes) induced pluripotent stem cell lines (iPSCs) into mesenchymal stem cells (MSCs) and subsequently into osteogenic cells (bone cells). We validated differentiation using standard methods and collected single-cell RNA sequencing data from over 100,000 cells across multiple samples and replicates at each stage of differentiation. While most genes that we examined display conserved patterns of expression across species, hundreds of genes are differentially expressed (DE) between humans and chimpanzees within and across stages of osteogenic differentiation. Some of these interspecific DE genes show functional enrichments relevant in skeletal tissue trait development. Moreover, topic modeling indicates that interspecific gene programs become more pronounced as cells mature. Overall, we propose that this in vitro model can be used to identify interspecific regulatory differences that may have contributed to skeletal trait differences between species. Public Library of Science 2022-03-09 /pmc/articles/PMC8936463/ /pubmed/35263340 http://dx.doi.org/10.1371/journal.pgen.1010073 Text en © 2022 Housman et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Housman, Genevieve Briscoe, Emilie Gilad, Yoav Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title | Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title_full | Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title_fullStr | Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title_full_unstemmed | Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title_short | Evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
title_sort | evolutionary insights into primate skeletal gene regulation using a comparative cell culture model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936463/ https://www.ncbi.nlm.nih.gov/pubmed/35263340 http://dx.doi.org/10.1371/journal.pgen.1010073 |
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