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Functional human genes typically exhibit epigenetic conservation

Recent DepMap CRISPR-Cas9 single gene disruptions have identified genes more essential to proliferation in tissue culture. It would be valuable to translate these finding with measurements more practical for human tissues. Here we show that DepMap essential genes and other literature curated functio...

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Autores principales: Rud, Daniel, Marjoram, Paul, Siegmund, Kimberly, Shibata, Darryl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439480/
https://www.ncbi.nlm.nih.gov/pubmed/34520456
http://dx.doi.org/10.1371/journal.pone.0253250
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author Rud, Daniel
Marjoram, Paul
Siegmund, Kimberly
Shibata, Darryl
author_facet Rud, Daniel
Marjoram, Paul
Siegmund, Kimberly
Shibata, Darryl
author_sort Rud, Daniel
collection PubMed
description Recent DepMap CRISPR-Cas9 single gene disruptions have identified genes more essential to proliferation in tissue culture. It would be valuable to translate these finding with measurements more practical for human tissues. Here we show that DepMap essential genes and other literature curated functional genes exhibit cell-specific preferential epigenetic conservation when DNA methylation measurements are compared between replicate cell lines and between intestinal crypts from the same individual. Culture experiments indicate that epigenetic drift accumulates through time with smaller differences in more functional genes. In NCI-60 cell lines, greater targeted gene conservation correlated with greater drug sensitivity. These studies indicate that two measurements separated in time allow normal or neoplastic cells to signal through conservation which human genes are more essential to their survival in vitro or in vivo.
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spelling pubmed-84394802021-09-15 Functional human genes typically exhibit epigenetic conservation Rud, Daniel Marjoram, Paul Siegmund, Kimberly Shibata, Darryl PLoS One Research Article Recent DepMap CRISPR-Cas9 single gene disruptions have identified genes more essential to proliferation in tissue culture. It would be valuable to translate these finding with measurements more practical for human tissues. Here we show that DepMap essential genes and other literature curated functional genes exhibit cell-specific preferential epigenetic conservation when DNA methylation measurements are compared between replicate cell lines and between intestinal crypts from the same individual. Culture experiments indicate that epigenetic drift accumulates through time with smaller differences in more functional genes. In NCI-60 cell lines, greater targeted gene conservation correlated with greater drug sensitivity. These studies indicate that two measurements separated in time allow normal or neoplastic cells to signal through conservation which human genes are more essential to their survival in vitro or in vivo. Public Library of Science 2021-09-14 /pmc/articles/PMC8439480/ /pubmed/34520456 http://dx.doi.org/10.1371/journal.pone.0253250 Text en © 2021 Rud 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
Rud, Daniel
Marjoram, Paul
Siegmund, Kimberly
Shibata, Darryl
Functional human genes typically exhibit epigenetic conservation
title Functional human genes typically exhibit epigenetic conservation
title_full Functional human genes typically exhibit epigenetic conservation
title_fullStr Functional human genes typically exhibit epigenetic conservation
title_full_unstemmed Functional human genes typically exhibit epigenetic conservation
title_short Functional human genes typically exhibit epigenetic conservation
title_sort functional human genes typically exhibit epigenetic conservation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439480/
https://www.ncbi.nlm.nih.gov/pubmed/34520456
http://dx.doi.org/10.1371/journal.pone.0253250
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