11 research outputs found

    DNA methylation analysis from saliva samples for epidemiological studies

    No full text
    <p>Saliva is a non-invasive, easily accessible tissue, which is regularly collected in large epidemiological studies to examine genetic questions. Recently, it is becoming more common to use saliva to assess DNA methylation. However, DNA extracted from saliva is a mixture of both bacterial and human DNA derived from epithelial and immune cells in the mouth. Thus, there are unique challenges to using salivary DNA in methylation studies that can influence data quality. This study assesses: (1) quantification of human DNA after extraction; (2) delineation of human and bacterial DNA; (3) bisulfite conversion (BSC); (4) quantification of BSC DNA; (5) PCR amplification of BSC DNA from saliva and; (6) quantitation of DNA methylation with a targeted assay. The framework proposed will allow saliva samples to be more widely used in targeted epigenetic studies.</p

    Fetal DNA Methylation Associates with Early Spontaneous Preterm Birth and Gestational Age

    Get PDF
    <div><p>Spontaneous preterm birth (PTB, <37 weeks gestation) is a major public health concern, and children born preterm have a higher risk of morbidity and mortality throughout their lives. Recent studies suggest that fetal DNA methylation of several genes varies across a range of gestational ages (GA), but it is not yet clear if fetal epigenetic changes associate with PTB. The objective of this study is to interrogate methylation patterns across the genome in fetal leukocyte DNA from African Americans with early PTB (24<sup>1/7</sup>–34<sup>0/7</sup> weeks; N = 22) or term births (39<sup>0/7</sup>–40<sup>6/7</sup>weeks; N = 28) and to evaluate the association of each CpG site with PTB and GA. DNA methylation was assessed across the genome with the HumanMethylation450 BeadChip. For each individual sample and CpG site, the proportion of DNA methylation was estimated. The associations between methylation and PTB or GA were evaluated by fitting a separate linear model for each CpG site, adjusting for relevant covariates. Overall, 29 CpG sites associated with PTB (FDR<.05; 5.7×10<sup>−10</sup>−6) independent of GA. Also, 9637 sites associated with GA (FDR<.05; 9.5×10<sup>−16</sup>−3), with 61.8% decreasing in methylation with shorter GA. GA-associated CpG sites were depleted in the CpG islands of their respective genes (p<2.2×10<sup>−16</sup>). Gene set enrichment analysis (GSEA) supported enrichment of GA-associated CpG sites in genes that play a role in embryonic development as well as the extracellular matrix. Additionally, this study replicated the association of several CpG sites associated with gestational age in other studies (<i>CRHBP</i>, <i>PIK3CD</i> and <i>AVP</i>). Dramatic differences in fetal DNA methylation are evident in fetuses born preterm versus at term, and the patterns established at birth may provide insight into the long-term consequences associated with PTB.</p></div

    Enrichment analysis to examine whether there is a an enrichment in certain regions that associated with GA, or whether there is an enrichment of a certain direction of a t-statistic for associated CpG sites.

    No full text
    <p>Note that each row in the table represents a Fisher’s exact test that tests for enrichment of associated or unassociated sites for the relevant category (e.g. CpG islands).</p>*<p>NS indicates the p-value is not significant (p>.05).</p

    Manhattan plots depicting the association of all CpG sites with (A) PTB and with (B) GA.

    No full text
    <p>The y-axis is the negative log10 of the p-value for the association while the x-axis is position on each chromosome. The dashed line indicates experiment-wide significance. Genomic locations of each CpG site are in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0067489#pone.0067489.s003" target="_blank">Table S1</a>.</p
    corecore