生物
DNA
大肠杆菌
DNA损伤
代谢物
遗传学
DNA加合物
癌变
生物化学
基因
作者
Matthew R. Wilson,Yindi Jiang,Peter W. Villalta,Alessia Stornetta,Paul D. Boudreau,Andrea Carrà,Caitlin A. Brennan,Eunyoung Chun,Lizzie Ngo,Leona D. Samson,Bevin P. Engelward,Wendy S. Garrett,Silvia Balbo,Emily P. Balskus
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-02-15
卷期号:363 (6428)
被引量:471
标识
DOI:10.1126/science.aar7785
摘要
Certain Escherichia coli strains residing in the human gut produce colibactin, a small-molecule genotoxin implicated in colorectal cancer pathogenesis. However, colibactin's chemical structure and the molecular mechanism underlying its genotoxic effects have remained unknown for more than a decade. Here we combine an untargeted DNA adductomics approach with chemical synthesis to identify and characterize a covalent DNA modification from human cell lines treated with colibactin-producing E. coli Our data establish that colibactin alkylates DNA with an unusual electrophilic cyclopropane. We show that this metabolite is formed in mice colonized by colibactin-producing E. coli and is likely derived from an initially formed, unstable colibactin-DNA adduct. Our findings reveal a potential biomarker for colibactin exposure and provide mechanistic insights into how a gut microbe may contribute to colorectal carcinogenesis.
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