Cargando…

Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans

A major concern in common disease epigenomics is distinguishing causal from consequential epigenetic variation. One means of addressing this issue is to identify the temporal origins of epigenetic variants via longitudinal analyses. However, prospective birth-cohort studies are expensive and time co...

Descripción completa

Detalles Bibliográficos
Autores principales: Beyan, Huriya, Down, Thomas A., Ramagopalan, Sreeram V., Uvebrant, Kristina, Nilsson, Anita, Holland, Michelle L., Gemma, Carolina, Giovannoni, Gavin, Boehm, Bernhard O., Ebers, George C., Lernmark, Åke, Cilio, Corrado M., Leslie, R. David, Rakyan, Vardhman K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483543/
https://www.ncbi.nlm.nih.gov/pubmed/22919074
http://dx.doi.org/10.1101/gr.134304.111
_version_ 1782248015808954368
author Beyan, Huriya
Down, Thomas A.
Ramagopalan, Sreeram V.
Uvebrant, Kristina
Nilsson, Anita
Holland, Michelle L.
Gemma, Carolina
Giovannoni, Gavin
Boehm, Bernhard O.
Ebers, George C.
Lernmark, Åke
Cilio, Corrado M.
Leslie, R. David
Rakyan, Vardhman K.
author_facet Beyan, Huriya
Down, Thomas A.
Ramagopalan, Sreeram V.
Uvebrant, Kristina
Nilsson, Anita
Holland, Michelle L.
Gemma, Carolina
Giovannoni, Gavin
Boehm, Bernhard O.
Ebers, George C.
Lernmark, Åke
Cilio, Corrado M.
Leslie, R. David
Rakyan, Vardhman K.
author_sort Beyan, Huriya
collection PubMed
description A major concern in common disease epigenomics is distinguishing causal from consequential epigenetic variation. One means of addressing this issue is to identify the temporal origins of epigenetic variants via longitudinal analyses. However, prospective birth-cohort studies are expensive and time consuming. Here, we report DNA methylomics of archived Guthrie cards for the retrospective longitudinal analyses of in-utero-derived DNA methylation variation. We first validate two methodologies for generating comprehensive DNA methylomes from Guthrie cards. Then, using an integrated epigenomic/genomic analysis of Guthrie cards and follow-up samplings, we identify interindividual DNA methylation variation that is present both at birth and 3 yr later. These findings suggest that disease-relevant epigenetic variation could be detected at birth, i.e., before overt clinical disease. Guthrie card methylomics offers a potentially powerful and cost-effective strategy for studying the dynamics of interindividual epigenomic variation in a range of common human diseases.
format Online
Article
Text
id pubmed-3483543
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-34835432013-05-01 Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans Beyan, Huriya Down, Thomas A. Ramagopalan, Sreeram V. Uvebrant, Kristina Nilsson, Anita Holland, Michelle L. Gemma, Carolina Giovannoni, Gavin Boehm, Bernhard O. Ebers, George C. Lernmark, Åke Cilio, Corrado M. Leslie, R. David Rakyan, Vardhman K. Genome Res Research A major concern in common disease epigenomics is distinguishing causal from consequential epigenetic variation. One means of addressing this issue is to identify the temporal origins of epigenetic variants via longitudinal analyses. However, prospective birth-cohort studies are expensive and time consuming. Here, we report DNA methylomics of archived Guthrie cards for the retrospective longitudinal analyses of in-utero-derived DNA methylation variation. We first validate two methodologies for generating comprehensive DNA methylomes from Guthrie cards. Then, using an integrated epigenomic/genomic analysis of Guthrie cards and follow-up samplings, we identify interindividual DNA methylation variation that is present both at birth and 3 yr later. These findings suggest that disease-relevant epigenetic variation could be detected at birth, i.e., before overt clinical disease. Guthrie card methylomics offers a potentially powerful and cost-effective strategy for studying the dynamics of interindividual epigenomic variation in a range of common human diseases. Cold Spring Harbor Laboratory Press 2012-11 /pmc/articles/PMC3483543/ /pubmed/22919074 http://dx.doi.org/10.1101/gr.134304.111 Text en © 2012, Published by Cold Spring Harbor Laboratory Press This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Beyan, Huriya
Down, Thomas A.
Ramagopalan, Sreeram V.
Uvebrant, Kristina
Nilsson, Anita
Holland, Michelle L.
Gemma, Carolina
Giovannoni, Gavin
Boehm, Bernhard O.
Ebers, George C.
Lernmark, Åke
Cilio, Corrado M.
Leslie, R. David
Rakyan, Vardhman K.
Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title_full Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title_fullStr Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title_full_unstemmed Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title_short Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
title_sort guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483543/
https://www.ncbi.nlm.nih.gov/pubmed/22919074
http://dx.doi.org/10.1101/gr.134304.111
work_keys_str_mv AT beyanhuriya guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT downthomasa guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT ramagopalansreeramv guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT uvebrantkristina guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT nilssonanita guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT hollandmichellel guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT gemmacarolina guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT giovannonigavin guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT boehmbernhardo guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT ebersgeorgec guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT lernmarkake guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT ciliocorradom guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT leslierdavid guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans
AT rakyanvardhmank guthriecardmethylomicsidentifiestemporallystableepiallelesthatarepresentatbirthinhumans