Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.

In storing and transmitting epigenetic information, organisms must balance the need to maintain information about past conditions with the capacity to respond to information in their current and future environments. Some of this information is encoded by DNA methylation, which can be transmitted wit...

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Main Authors: Minseung Choi, Diane P Genereux, Jamie Goodson, Haneen Al-Azzawi, Shannon Q Allain, Noah Simon, Stan Palasek, Carol B Ware, Chris Cavanaugh, Daniel G Miller, Winslow C Johnson, Kevin D Sinclair, Reinhard Stöger, Charles D Laird
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-11-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5690686?pdf=render
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spelling doaj-b967721753764a2fae9f6e07de2743872020-11-25T00:53:56ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042017-11-011311e100706010.1371/journal.pgen.1007060Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.Minseung ChoiDiane P GenereuxJamie GoodsonHaneen Al-AzzawiShannon Q AllainNoah SimonStan PalasekCarol B WareChris CavanaughDaniel G MillerWinslow C JohnsonKevin D SinclairReinhard StögerCharles D LairdIn storing and transmitting epigenetic information, organisms must balance the need to maintain information about past conditions with the capacity to respond to information in their current and future environments. Some of this information is encoded by DNA methylation, which can be transmitted with variable fidelity from parent to daughter strand. High fidelity confers strong pattern matching between the strands of individual DNA molecules and thus pattern stability over rounds of DNA replication; lower fidelity confers reduced pattern matching, and thus greater flexibility. Here, we present a new conceptual framework, Ratio of Concordance Preference (RCP), that uses double-stranded methylation data to quantify the flexibility and stability of the system that gave rise to a given set of patterns. We find that differentiated mammalian cells operate with high DNA methylation stability, consistent with earlier reports. Stem cells in culture and in embryos, in contrast, operate with reduced, albeit significant, methylation stability. We conclude that preference for concordant DNA methylation is a consistent mode of information transfer, and thus provides epigenetic stability across cell divisions, even in stem cells and those undergoing developmental transitions. Broader application of our RCP framework will permit comparison of epigenetic-information systems across cells, developmental stages, and organisms whose methylation machineries differ substantially or are not yet well understood.http://europepmc.org/articles/PMC5690686?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Minseung Choi
Diane P Genereux
Jamie Goodson
Haneen Al-Azzawi
Shannon Q Allain
Noah Simon
Stan Palasek
Carol B Ware
Chris Cavanaugh
Daniel G Miller
Winslow C Johnson
Kevin D Sinclair
Reinhard Stöger
Charles D Laird
spellingShingle Minseung Choi
Diane P Genereux
Jamie Goodson
Haneen Al-Azzawi
Shannon Q Allain
Noah Simon
Stan Palasek
Carol B Ware
Chris Cavanaugh
Daniel G Miller
Winslow C Johnson
Kevin D Sinclair
Reinhard Stöger
Charles D Laird
Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
PLoS Genetics
author_facet Minseung Choi
Diane P Genereux
Jamie Goodson
Haneen Al-Azzawi
Shannon Q Allain
Noah Simon
Stan Palasek
Carol B Ware
Chris Cavanaugh
Daniel G Miller
Winslow C Johnson
Kevin D Sinclair
Reinhard Stöger
Charles D Laird
author_sort Minseung Choi
title Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
title_short Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
title_full Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
title_fullStr Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
title_full_unstemmed Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells.
title_sort epigenetic memory via concordant dna methylation is inversely correlated to developmental potential of mammalian cells.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2017-11-01
description In storing and transmitting epigenetic information, organisms must balance the need to maintain information about past conditions with the capacity to respond to information in their current and future environments. Some of this information is encoded by DNA methylation, which can be transmitted with variable fidelity from parent to daughter strand. High fidelity confers strong pattern matching between the strands of individual DNA molecules and thus pattern stability over rounds of DNA replication; lower fidelity confers reduced pattern matching, and thus greater flexibility. Here, we present a new conceptual framework, Ratio of Concordance Preference (RCP), that uses double-stranded methylation data to quantify the flexibility and stability of the system that gave rise to a given set of patterns. We find that differentiated mammalian cells operate with high DNA methylation stability, consistent with earlier reports. Stem cells in culture and in embryos, in contrast, operate with reduced, albeit significant, methylation stability. We conclude that preference for concordant DNA methylation is a consistent mode of information transfer, and thus provides epigenetic stability across cell divisions, even in stem cells and those undergoing developmental transitions. Broader application of our RCP framework will permit comparison of epigenetic-information systems across cells, developmental stages, and organisms whose methylation machineries differ substantially or are not yet well understood.
url http://europepmc.org/articles/PMC5690686?pdf=render
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