Active DNA demethylation in mammals involves Ten-eleven translocation (TET) family proteins-mediated oxidation of 5-methylcytosine (5mC). However, base-resolution landscapes of 5-formylcytosine (5fC, an oxidized derivative of 5mC) at the single-cell level remains unexplored. Here we present “CLEVER-seq”, which is a single-cell, single-base resolution 5fC sequencing technology, based on biocompatible, selective chemical labeling of 5fC and subsequent C-to-T conversion during amplification and sequencing. CLEVER-seq of mouse early embryos reveals the highly patterned genomic distribution and parental specific dynamics of 5fC during mouse early pre-implantation development and synergistic 5fC production in paternal and maternal genomes. Integrated analysis demonstrates that promoter 5fC production precedes the expression upregulation of a clear set of developmentally and metabolically critical genes. Collectively, our work reveals the dynamics of active DNA demethylation during early mouse pre-implantation development and provides an important resource for further functional studies of epigenetic reprogramming in single cells.
Overall design: We developed a novel single-cell 5fC sequencing technique, termed “CLEVER-seq” (chemical labeling enabled C-to-T conversion sequencing), to map the genome-wide base resolution 5fC landscapes in mouse early embryos at single-cell level. We applied CLEVER-seq to mESCs (2i), mouse sperm, metaphase II oocytes, zygotes, 2-cell embryos, 4-cell embryos, inner cell mass (ICM) and trophectoderm (TE). The male and female pronuclei within each individual PN3-PN4 stage zygote were physically isolated by micromanipulation; the individual blasotomeres of 2-cell and 4-cell embryos were also separated. In addition to mESCs (2i), we also performed CLEVER-seq to mESCs (serum), mEpiSCs, and hESCs. In total, we sequenced more than 1,500 GB data for 139 single cells, and identified 3,216-41,347 5fCpG sites from these samples.
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