An allele-resolved nanopore-guided tour of the human placental methylome

The placenta is a temporary organ present during pregnancy that is responsible for coordinating all aspects of pregnancy between the mother and fetus. It has a distinct epigenetic, transcriptomic, and mutational landscape with low levels of methylation, high numbers of transcribed loci, and a high mutational burden relative to somatic tissues. We present this landscape through the application of nanopore sequencing technology to provide a more comprehensive picture of female placental genomics and methylomics along with integrated haplotype-resolved transcriptomic analyses across eight trios. Whole genome sequencing of trios allows robust phasing, permitting comprehensive genome-wide investigation of parent-of-origin methylation and transcription. This enhanced view facilitates identifications of many differentially methylated regions (DMRs), both conserved and differing between individuals, as well as previously unreported imprinted genes including ILDR2 and RASA1 which are potentially important for healthy placental and fetal development.

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Publication Details

Journal
Nature Communications
Published
2025-11-24
DOI
https://doi.org/10.1038/s41467-025-65337-3
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
0.00

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article

An allele-resolved nanopore-guided tour of the human placental methylome

Michaela Kindlova, Adam D. Ewing, Jade M Kubler, Danielle J. Borg et al.
Nature Communications
Genetic Syndromes and Imprinting
article

An allele-resolved nanopore-guided tour of the human placental methylome

Michaela Kindlova, Adam D. Ewing, Jade M Kubler, Danielle J. Borg, Jessica Whyte, Sarah E. Steane, Vicki Lee Clifton, Hannah Byrne
article en

Abstract

The placenta is a temporary organ present during pregnancy that is responsible for coordinating all aspects of pregnancy between the mother and fetus. It has a distinct epigenetic, transcriptomic, and mutational landscape with low levels of methylation, high numbers of transcribed loci, and a high mutational burden relative to somatic tissues. We present this landscape through the application of nanopore sequencing technology to provide a more comprehensive picture of female placental genomics and methylomics along with integrated haplotype-resolved transcriptomic analyses across eight trios. Whole genome sequencing of trios allows robust phasing, permitting comprehensive genome-wide investigation of parent-of-origin methylation and transcription. This enhanced view facilitates identifications of many differentially methylated regions (DMRs), both conserved and differing between individuals, as well as previously unreported imprinted genes including ILDR2 and RASA1 which are potentially important for healthy placental and fetal development.

Nature CommunicationsVol. 16(1)
The University of Queensland (AU), Mater Research (AU)
Mater Foundation, Advance Queensland
Openalex Percentile: Top 62%
Genetic Syndromes and Imprinting
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An allele-resolved nanopore-guided tour of the human placental methylome — Michaela Kindlova, Adam D. Ewing, et al. · Nature Communications (2025) | TGRS Research Map | TGRS