Genome-wide mapping reveals that deoxyuridine is enriched in the human centromeric DNA

被引:49
作者
Shu, Xiaoting [1 ,2 ,3 ]
Liu, Menghao [1 ,2 ,3 ]
Lu, Zhike [1 ,2 ]
Zhu, Chenxu [1 ,2 ]
Meng, Haowei [1 ,2 ]
Huang, Sihao [1 ,2 ]
Zhang, Xiaoxue [3 ]
Yi, Chengqi [1 ,2 ,4 ,5 ]
机构
[1] Peking Univ, Sch Life Sci, State Key Lab Prot & Plant Gene Res, Beijing, Peoples R China
[2] Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
[3] Peking Univ, Acad Adv Interdisciplinary Studies, Beijing, Peoples R China
[4] Peking Univ, Dept Chem Biol, Coll Chem & Mol Engn, Beijing, Peoples R China
[5] Peking Univ, Synthet & Funct Biomol Ctr, Coll Chem & Mol Engn, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
BASE-EXCISION-REPAIR; URACIL; GLYCOSYLASES; CELLS; MECHANISM; PROTEINS; 5-FORMYLCYTOSINE; REPLICATION; METHYLATION; DEAMINATION;
D O I
10.1038/s41589-018-0065-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Uracil in DNA can be generated by cytosine deamination or dUMP misincorporation; however, its distribution in the human genome is poorly understood. Here we present a selective labeling and pull-down technology for genome-wide uracil profiling and identify thousands of uracil peaks in three different human cell lines. Surprisingly, uracil is highly enriched at the centromere of the human genome. Using mass spectrometry, we demonstrate that human centromeric DNA contains a higher level of uracil. We also directly verify the presence of uracil within two centromeric uracil peaks on chromosomes 6 and 11. Moreover, centromeric uracil is preferentially localized within the binding regions of the centromere-specific histone CENP-A and can be excised by human uracil-DNA glycosylase UNG. Collectively, our approaches allow comprehensive analysis of uracil in the human genome and provide robust tools for mapping and future functional studies of uracil in DNA.
引用
收藏
页码:680 / +
页数:10
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