| Literature DB >> 30278133 |
Hu Zeng1, Bo He2, Bo Xia1, Dongsheng Bai1, Xingyu Lu3, Jiabin Cai4, Lei Chen5, Ankun Zhou1, Chenxu Zhu1, Haowei Meng1, Yun Gao6, Hongshan Guo6, Chuan He7,8, Qing Dai7, Chengqi Yi1,2,8.
Abstract
High-resolution detection of genome-wide 5-hydroxymethylcytosine (5hmC) sites of small-scale samples remains challenging. Here, we present hmC-CATCH, a bisulfite-free, base-resolution method for the genome-wide detection of 5hmC. hmC-CATCH is based on selective 5hmC oxidation, chemical labeling and subsequent C-to-T transition during PCR. Requiring only nanoscale input genomic DNA samples, hmC-CATCH enabled us to detect genome-wide hydroxymethylome of human embryonic stem cells in a cost-effective manner. Further application of hmC-CATCH to cell-free DNA (cfDNA) of healthy donors and cancer patients revealed base-resolution hydroxymethylome in the human cfDNA for the first time. We anticipate that our chemical biology approach will find broad applications in hydroxymethylome analysis of limited biological and clinical samples.Entities:
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Year: 2018 PMID: 30278133 PMCID: PMC6423965 DOI: 10.1021/jacs.8b08297
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419