Nature BiotechnologyGenomicsPeer-reviewed journal article
Quantitative single cell 5hmC sequencing reveals non-canonical gene regulation by non-CG hydroxymethylation
Emily B. FabyaniciD, Peng HuiD, Qi QiuiD, Kiara N. BerríosiD, Daniel R. ConnollyiD, Tong WangiD, Jennifer Flournoy, Zhaolan ZhouiD, Rahul M. KohliiD, Hao WuiD
Abstract
Oxidative modification of 5-methylcytosine (5mC) generates 5-hydroxymethylcytosine (5hmC), a DNA modification that exhibits unique epigenetic regulatory functions and impacts diverse biological processes. However, standard single-nucleus/cell bisulfite sequencing methods cannot resolve the base ambiguity between 5mC and 5hmC to accurately measure cell-type specific epigenomic patterns and gene regulatory functions of 5hmC or true 5mC. Here, we develop single-nucleus 5hmC sequencing (snhmC-seq) for quantitative and unbiased 5hmC profiling in single cells by harnessing differential deaminase activity of APOBEC3A towards 5mC and chemically protected 5hmC. We used snhmC-seq to profile single nuclei from cryopreserved mouse brain samples to reveal epigenetic heterogeneity of 5hmC at single-cell resolution and uncovered a non-canonical gene regulatory role of genic 5hmC in non-CG context.
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