Erik S Carlson, Raphael Haslecker, Chiara Lecchi, Miguel A Aguilar Ramos, Vyshnavi Vennelakanti, Linda Honaker, Alessia Stornetta, Estela S Millán, Bruce A Johnson, Heather J Kulik, Silvia Balbo, Peter W Villalta, Victoria D'Souza, Emily P Balskus
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引用次数: 0
摘要
越来越多的证据表明,化学上不稳定、破坏dna的肠道细菌天然产物大肠杆菌素与结直肠癌有关,包括鉴定出被认为是由大肠杆菌素- dna链间交联(ICLs)引起的突变特征。然而,我们目前缺乏关于该病变结构的直接信息。在这里,我们结合质谱和核磁共振波谱来阐明大肠杆菌素- dna ICL的特异性和结构。我们发现大肠杆菌蛋白在富含at的DNA的小槽内烷基化,解释了突变特征的起源。出乎意料的是,我们发现化学上不稳定的大肠杆菌蛋白中心基序介导了交联的序列特异性。通过直接阐明大肠杆菌蛋白与DNA的相互作用,这项工作增强了我们对这种独特的与癌症相关的肠道细菌天然产物的结构和遗传毒性机制的理解。
The specificity and structure of DNA crosslinking by the gut bacterial genotoxin colibactin.
Accumulating evidence has connected the chemically unstable, DNA-damaging gut bacterial natural product colibactin to colorectal cancer, including the identification of mutational signatures that are thought to arise from colibactin-DNA interstrand crosslinks (ICLs). However, we currently lack direct information regarding the structure of this lesion. Here, we combine mass spectrometry and nuclear magnetic resonance spectroscopy to elucidate the specificity and structure of the colibactin-DNA ICL. We find that colibactin alkylates within the minor groove of AT-rich DNA, explaining the origins of mutational signatures. Unexpectedly, we discover that the chemically unstable central motif of colibactin mediates the sequence specificity of crosslinking. By directly elucidating colibactin's interactions with DNA, this work enhances our understanding of the structure and genotoxic mechanisms of this cancer-linked gut bacterial natural product.