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DNA METHYLATION CLOCKS IN MOUSE

One of important limiting factors in aging research is the time required to measure the effect of an intervention on lifespan. But this situation is now changing due to a recent discovery of DNA methylation-based markers (DNAm clocks). We developed a whole lifespan multi-tissue DNAm clock for mice w...

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Detalles Bibliográficos
Autores principales: Meer, Margarita, Gladyshev, Vadim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845197/
http://dx.doi.org/10.1093/geroni/igz038.3516
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author Meer, Margarita
Gladyshev, Vadim
author_facet Meer, Margarita
Gladyshev, Vadim
author_sort Meer, Margarita
collection PubMed
description One of important limiting factors in aging research is the time required to measure the effect of an intervention on lifespan. But this situation is now changing due to a recent discovery of DNA methylation-based markers (DNAm clocks). We developed a whole lifespan multi-tissue DNAm clock for mice with R2 =0.89. We also carried out comparative analyses of the available mouse DNAm clocks (single- or multi-tissue, based on different number of sites, based on one genomic locus or multi-loci). In general, tissue specific clocks are more accurate than muti-tissue clocks. We applied these tools to a variety of experimental systems, ranging from interventions to rejuvenation approaches, and analyzed various mouse tissues and public datasets. We further applied DNAm clocks to newly sequenced sets of blood and liver samples. Multi-loci blood clock outperforms other clocks when applied to blood samples, and the liver and multi-tissue clocks show similar precision on liver.
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spelling pubmed-68451972019-11-18 DNA METHYLATION CLOCKS IN MOUSE Meer, Margarita Gladyshev, Vadim Innov Aging Session Lb3620 (Late Breaking Poster) One of important limiting factors in aging research is the time required to measure the effect of an intervention on lifespan. But this situation is now changing due to a recent discovery of DNA methylation-based markers (DNAm clocks). We developed a whole lifespan multi-tissue DNAm clock for mice with R2 =0.89. We also carried out comparative analyses of the available mouse DNAm clocks (single- or multi-tissue, based on different number of sites, based on one genomic locus or multi-loci). In general, tissue specific clocks are more accurate than muti-tissue clocks. We applied these tools to a variety of experimental systems, ranging from interventions to rejuvenation approaches, and analyzed various mouse tissues and public datasets. We further applied DNAm clocks to newly sequenced sets of blood and liver samples. Multi-loci blood clock outperforms other clocks when applied to blood samples, and the liver and multi-tissue clocks show similar precision on liver. Oxford University Press 2019-11-08 /pmc/articles/PMC6845197/ http://dx.doi.org/10.1093/geroni/igz038.3516 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Session Lb3620 (Late Breaking Poster)
Meer, Margarita
Gladyshev, Vadim
DNA METHYLATION CLOCKS IN MOUSE
title DNA METHYLATION CLOCKS IN MOUSE
title_full DNA METHYLATION CLOCKS IN MOUSE
title_fullStr DNA METHYLATION CLOCKS IN MOUSE
title_full_unstemmed DNA METHYLATION CLOCKS IN MOUSE
title_short DNA METHYLATION CLOCKS IN MOUSE
title_sort dna methylation clocks in mouse
topic Session Lb3620 (Late Breaking Poster)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845197/
http://dx.doi.org/10.1093/geroni/igz038.3516
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