Journal article
Genome-wide analysis of DNA methylation in human amnion
TheScientificWorld, Vol.2013, 678156
2013
DOI: 10.1155/2013/678156
PMCID: PMC3590748
PMID: 23533356
Abstract
The amnion is a specialized tissue in contact with the amniotic fluid, which is in a constantly changing state. To investigate the importance of epigenetic events in this tissue in the physiology and pathophysiology of pregnancy, we performed genome-wide DNA methylation profiling of human amnion from term (with and without labor) and preterm deliveries. Using the Illumina Infinium HumanMethylation27 BeadChip, we identified genes exhibiting differential methylation associated with normal labor and preterm birth. Functional analysis of the differentially methylated genes revealed biologically relevant enriched gene sets. Bisulfite sequencing analysis of the promoter region of the oxytocin receptor (OXTR) gene detected two CpG dinucleotides showing significant methylation differences among the three groups of samples. Hypermethylation of the CpG island of the solute carrier family 30 member 3 (SLC30A3) gene in preterm amnion was confirmed by methylation-specific PCR. This work provides preliminary evidence that DNA methylation changes in the amnion may be at least partially involved in the physiological process of labor and the etiology of preterm birth and suggests that DNA methylation profiles, in combination with other biological data, may provide valuable insight into the mechanisms underlying normal and pathological pregnancies.
Details
- Title: Subtitle
- Genome-wide analysis of DNA methylation in human amnion
- Creators
- Jinsil Kim - Department of Anatomy and Cell Biology, University of Iowa, 500 Newton Road, 2182 ML, Iowa City, IA 52242, USAMitchell M PitlickPaul J ChristineAmanda R SchaeferCesar SalemeBelén ComasViviana CosentinoEnrique GadowJeffrey C Murray
- Resource Type
- Journal article
- Publication Details
- TheScientificWorld, Vol.2013, 678156
- DOI
- 10.1155/2013/678156
- PMID
- 23533356
- PMCID
- PMC3590748
- NLM abbreviation
- ScientificWorldJournal
- ISSN
- 1537-744X
- eISSN
- 1537-744X
- Publisher
- United States
- Grant note
- R01 HD057192 / NICHD NIH HHS P30 ES005605 / NIEHS NIH HHS R01 HD052953 / NICHD NIH HHS HD57192 / NICHD NIH HHS
- Language
- English
- Date published
- 2013
- Academic Unit
- Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Dental Research
- Record Identifier
- 9984025349002771
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