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Heikkinen, A.

Publications and source records attributed to Heikkinen, A..

2 recordsLinked to original sources

DNA methylation sites in early adulthood characterised by pubertal timing and development: A twin study

BackgroundPuberty is a highly heritable and variable trait, with environmental factors having a role in its eventual timing and development. Early and late pubertal onset are both associated with various diseases developing later in life, and epigenetic characterisation of pubertal timing and development could lead to important insights. Blood DNA methylation, reacting to both genotype and environment, has been associated with puberty; however, such studies are relatively scarce. We investigated peripheral blood DNA methylation profiles (using Illumina 450K and EPIC platforms) of 1539 young adult Finnish twins associated with pubertal development scale (PDS) and pubertal age (PA). ResultsFixed effect meta-analysis of the two platforms on 347521 CpGs in common identified 58 CpG sites associated (p < 1 x 10-5) with either PDS or PA. All four CpGs associated with PA and 45 CpGs associated with PDS were sex specific. Thirteen CpGs had a high heritability (h2: 0.51-0.98), while one CpG site (mapped to GET4) had a high shared environmental component accounting for 68% of the overall variance in methylation at the site. Utilising twin discordance analysis, we found 6 CpG sites (5 associated with PDS and 1 with PA) that had an environmentally driven association with puberty. Furthermore, genes with PDS- or PA-associated CpGs were linked to various developmental processes and diseases, such as breast, prostate and ovarian cancer, while methylation quantitative trait loci (meQTLs) of associated CpG sites were enriched in immune pathways developing during puberty. ConclusionsBy identifying puberty-associated DNA methylation sites and examining the effects of sex, environment and genetics, we shed light on the intricate interplay between environment and genetics in the context of puberty. Through our comprehensive analysis, we not only deepen the understanding of the significance of both genetic and environmental factors in the complex processes of puberty and its timing but also gain insights into potential links with disease risks.

genomics↗

Methylation status of VTRNA2-1/nc886 is stable across human populations, monozygotic twin pairs and in majority of somatic tissues

Aims and methodsOur aim was to characterise the methylation level of a polymorphically imprinted gene, VTRNA2-1/nc886, in human populations and somatic tissues. We utilised 48 datasets, consisting of >30 different tissues and >30 000 individuals. ResultsWe show that the nc886 methylation status is associated with twin status and ethnic background, but the variation between populations is limited. Monozygotic twin pairs present concordant methylation, while [~]30% of dizygotic twin pairs present discordant methylation in the nc886 locus. The methylation levels of nc886 are uniform across somatic tissues, except in cerebellum and skeletal muscle. ConclusionWe hypothesize that the nc886 imprint is established in the oocyte and that after implantation, the methylation status is stable, excluding a few specific tissues.

molecular biology↗