11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome

Background Prenatal growth restriction and low birth weight have been linked to long-term alterations of health, presumably via adaptive modifications of the epigenome. Recent studies indicate a plasticity of the 11p15 epigenotype in response to environmental changes during early stages of human dev...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: El Maarri, Osman (author)
مؤلفون آخرون: Schreiner, Felix (author), Gohlke, Bettina (author), Stutte, Sonja (author), Bartmann, Peter (author), Hecher, Kurt (author), Oldenburg, Johannes (author), Woelfle, Joachim (author)
التنسيق: article
منشور في: 2013
الوصول للمادة أونلاين:http://hdl.handle.net/10725/6195
https://doi.org/10.1186/1868-7083-6-6
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/1868-7083-6-6
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_version_ 1864513478886162432
author El Maarri, Osman
author2 Schreiner, Felix
Gohlke, Bettina
Stutte, Sonja
Bartmann, Peter
Hecher, Kurt
Oldenburg, Johannes
Woelfle, Joachim
author2_role author
author
author
author
author
author
author
author_facet El Maarri, Osman
Schreiner, Felix
Gohlke, Bettina
Stutte, Sonja
Bartmann, Peter
Hecher, Kurt
Oldenburg, Johannes
Woelfle, Joachim
author_role author
dc.creator.none.fl_str_mv El Maarri, Osman
Schreiner, Felix
Gohlke, Bettina
Stutte, Sonja
Bartmann, Peter
Hecher, Kurt
Oldenburg, Johannes
Woelfle, Joachim
dc.date.none.fl_str_mv 2013
2017-09-14T12:49:01Z
2017-09-14T12:49:01Z
2017-09-14
dc.identifier.none.fl_str_mv 1868-7083
http://hdl.handle.net/10725/6195
https://doi.org/10.1186/1868-7083-6-6
Schreiner, F., Gohlke, B., Stutte, S., Bartmann, P., Hecher, K., Oldenburg, J., ... & Woelfle, J. (2014). 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome. Clinical epigenetics, 6(1), 6.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/1868-7083-6-6
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Clinical Epigenetics
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Background Prenatal growth restriction and low birth weight have been linked to long-term alterations of health, presumably via adaptive modifications of the epigenome. Recent studies indicate a plasticity of the 11p15 epigenotype in response to environmental changes during early stages of human development. Study design We analyzed methylation levels at different 11p15 loci in 20 growth-discordant monozygotic twin pairs. Intrauterine development was discordant due to severe twin-to-twin transfusion syndrome (TTTS), which was treated by fetoscopic laser coagulation of communicating vessels before 25 weeks of gestation. Methylation levels at age 4 were determined in blood and buccal cell-derived DNA by the single nucleotide primer extension reaction ion pair reverse-phase high performance liquid chromatography (SNuPE IP RP HPLC) assay. Methylation at LINE-1 repeats was analyzed as an estimate of global methylation. Results In general, variance of locus-specific methylation levels appeared to be higher in buccal cell- as compared to blood cell-derived DNA samples. Paired analyses within the twin pairs revealed significant differences at only one CpG site (IGF2 dmr0 SN3 (blood), +1.9% in donors; P = 0.013). When plotting the twin pair-discordance in birth weight against the degree of discordance in site-specific methylation at age 4, only a few CpGs were found to interact (one CpG site each at IGF2dmr0 in blood/saliva DNA, one CpG at LINE-1 repeats in saliva DNA), with 26 to 36% of the intra-twin pair divergence at these sites explained by prenatal growth discordance. However, across the entire cohort of 40 children, site-specific methylation did not correlate with SD-scores for weight or length at birth. Insulin-like growth factor-II serum concentrations showed significant within-twin pair correlations at birth (R = 0.57) and at age 4 (R = 0.79), but did not differ between donors and recipients. They also did not correlate with the analyzed 11p15 methylation parameters. Conclusion In a cohort of 20 growth-discordant monozygotic twin pairs, severe alteration in placental blood supply due to TTTS appears to leave only weak, if any, epigenetic marks at the analyzed CpG sites at 11p15.
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identifier_str_mv 1868-7083
Schreiner, F., Gohlke, B., Stutte, S., Bartmann, P., Hecher, K., Oldenburg, J., ... & Woelfle, J. (2014). 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome. Clinical epigenetics, 6(1), 6.
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network_acronym_str LAURepo
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oai_identifier_str oai:laur.lau.edu.lb:10725/6195
publishDate 2013
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spelling 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndromeEl Maarri, OsmanSchreiner, FelixGohlke, BettinaStutte, SonjaBartmann, PeterHecher, KurtOldenburg, JohannesWoelfle, JoachimBackground Prenatal growth restriction and low birth weight have been linked to long-term alterations of health, presumably via adaptive modifications of the epigenome. Recent studies indicate a plasticity of the 11p15 epigenotype in response to environmental changes during early stages of human development. Study design We analyzed methylation levels at different 11p15 loci in 20 growth-discordant monozygotic twin pairs. Intrauterine development was discordant due to severe twin-to-twin transfusion syndrome (TTTS), which was treated by fetoscopic laser coagulation of communicating vessels before 25 weeks of gestation. Methylation levels at age 4 were determined in blood and buccal cell-derived DNA by the single nucleotide primer extension reaction ion pair reverse-phase high performance liquid chromatography (SNuPE IP RP HPLC) assay. Methylation at LINE-1 repeats was analyzed as an estimate of global methylation. Results In general, variance of locus-specific methylation levels appeared to be higher in buccal cell- as compared to blood cell-derived DNA samples. Paired analyses within the twin pairs revealed significant differences at only one CpG site (IGF2 dmr0 SN3 (blood), +1.9% in donors; P = 0.013). When plotting the twin pair-discordance in birth weight against the degree of discordance in site-specific methylation at age 4, only a few CpGs were found to interact (one CpG site each at IGF2dmr0 in blood/saliva DNA, one CpG at LINE-1 repeats in saliva DNA), with 26 to 36% of the intra-twin pair divergence at these sites explained by prenatal growth discordance. However, across the entire cohort of 40 children, site-specific methylation did not correlate with SD-scores for weight or length at birth. Insulin-like growth factor-II serum concentrations showed significant within-twin pair correlations at birth (R = 0.57) and at age 4 (R = 0.79), but did not differ between donors and recipients. They also did not correlate with the analyzed 11p15 methylation parameters. Conclusion In a cohort of 20 growth-discordant monozygotic twin pairs, severe alteration in placental blood supply due to TTTS appears to leave only weak, if any, epigenetic marks at the analyzed CpG sites at 11p15.PublishedN/A2017-09-14T12:49:01Z2017-09-14T12:49:01Z20132017-09-14Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1868-7083http://hdl.handle.net/10725/6195https://doi.org/10.1186/1868-7083-6-6Schreiner, F., Gohlke, B., Stutte, S., Bartmann, P., Hecher, K., Oldenburg, J., ... & Woelfle, J. (2014). 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome. Clinical epigenetics, 6(1), 6.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/1868-7083-6-6enClinical Epigeneticsinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/61952021-03-19T10:43:09Z
spellingShingle 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
El Maarri, Osman
status_str publishedVersion
title 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
title_full 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
title_fullStr 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
title_full_unstemmed 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
title_short 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
title_sort 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
url http://hdl.handle.net/10725/6195
https://doi.org/10.1186/1868-7083-6-6
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/1868-7083-6-6