Decoding dynamic epigenetic landscapes in human oocytes using single-cell multi-omics sequencing

Developing female human germ cells undergo genome-wide epigenetic reprogramming, but de novo DNA methylation dynamics and their interplay with chromatin states and transcriptional activation in developing oocytes is poorly understood. Here, we developed a single-cell multi-omics sequencing method, scChaRM-seq, that enables simultaneous profiling of the DNA methylome, transcriptome, and chromatin accessibility in single human oocytes and ovarian somatic cells. We observed a global increase in DNA methylation during human oocyte growth that correlates with chromatin accessibility, whereas increases of DNA methylation at specific features were associated with active transcription. Integrated analyses of multi-omics data from humans and mice revealed species-specific gene expression, and promoter accessibility contributes to gene body methylation programs. Alu elements retained low DNA methylation levels and high accessibility in early growing oocytes and were located near developmental genes in humans and mice. Together, these findings show how scChaRM-seq can provide insight into DNA methylation pattern establishment.

Automated summary

The research developed a novel single-cell multi-omics sequencing method and found that DNA methylation in human oocytes increases globally during growth, correlating with chromatin accessibility, while specific features of DNA methylation increase with active transcription. Integrated analysis of multi-omics data revealed species-specific gene expression and promoter accessibility contributing to gene body methylation programs.