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Effect of prematurity on genome wide methylation in the placenta.


ABSTRACT: BACKGROUND:Preterm birth is a significant clinical problem and an enormous burden on society, affecting one in eight pregnant women and their newborns. Despite decades of research, the molecular mechanism underlying its pathogenesis remains unclear. Many studies have shown that preterm birth is associated with health risks across the later life course. The "fetal origins" hypothesis postulates that adverse intrauterine exposures are associated with later disease susceptibility. Our recent studies have focused on the placental epigenome at term. We extended these studies to genome-wide placental DNA methylation across a wide range of gestational ages. We applied methylation dependent immunoprecipitation/DNA sequencing (MeDIP-seq) to 9 placentas with gestational age from 25?weeks to term to identify differentially methylated regions (DMRs). RESULTS:Enrichment analysis revealed 427 DMRs with nominally significant differences in methylation between preterm and term placentas (p?

SUBMITTER: Schuster J 

PROVIDER: S-EPMC6599230 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Effect of prematurity on genome wide methylation in the placenta.

Schuster Jessica J   Uzun Alper A   Stablia Joan J   Schorl Christoph C   Mori Mari M   Padbury James F JF  

BMC medical genetics 20190628 1


<h4>Background</h4>Preterm birth is a significant clinical problem and an enormous burden on society, affecting one in eight pregnant women and their newborns. Despite decades of research, the molecular mechanism underlying its pathogenesis remains unclear. Many studies have shown that preterm birth is associated with health risks across the later life course. The "fetal origins" hypothesis postulates that adverse intrauterine exposures are associated with later disease susceptibility. Our recen  ...[more]

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