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Quantitative mapping of DNA phosphorothioatome reveals phosphorothioate heterogeneity of low modification frequency

机译:DNA硫代磷原子的定量定位揭示了低修饰频率的硫代磷酸酯异质性

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Phosphorothioate (PT) modifications of the DNA backbone, widespread in prokaryotes, are first identified in bacterial enteropathogens Escherichia coli B7A more than a decade ago. However, methods for high resolution mapping of PT modification level are still lacking. Here, we developed the PT-IC-seq technique, based on iodine-induced selective cleavage at PT sites and high-throughput next generation sequencing, as a mean to quantitatively characterizing the genomic landscape of PT modifications. Using PT-IC-seq we foud that most PT sites are partially modified at a lower PT frequency (& 5%) in E . coli B7A and Salmonella enterica serovar Cerro 87, and both show a heterogeneity pattern of PT modification similar to those of the typical methylation modification. Combining the iodine-induced cleavage and absolute quantification by droplet digital PCR, we developed the PT-IC-ddPCR technique to further measure the PT modification level. Consistent with the PT-IC-seq measurements, PT-IC-ddPCR analysis confirmed the lower PT frequency in E . coli B7A. Our study has demonstrated the heterogeneity of PT modification in the bacterial population and we also established general tools for rigorous mapping and characterization of PT modification events at whole genome level. We describe to our knowledge the first genome-wide quantitative characterization of PT landscape and provides appropriate strategies for further functional studies of PT modification. Author summary Phosphorothioate (PT) modification is a novel DNA modification, previous studies showed that PT modifications in E . coli occure at G _(ps)AAC/G _(ps)TTC motifs, but the modification frequency at each site are not known. In this study, we introduced two methods: PT-IC-seq, which could quantitatively characterize the genomic landscape of PT modifications; and PT-IC-ddPCR, which could measure PT modification frequency precisely. Through these two new methods, heterogeneity, an important feature of PT modification, is revealed intuitively and accurately. The modifications revealed in this study provide a basis for the final revelation of the physiological functions of PT and give valuable reference for other DNA modification studies.
机译:DNA骨架的硫代磷酸酯(PT)修饰广泛存在于原核生物中,十多年前才在细菌性肠病原菌大肠杆菌B7A中被鉴定出来。但是,仍然缺少用于PT修改级别的高分辨率映射的方法。在这里,我们开发了PT-IC-seq技术,该技术基于碘诱导的PT位点的选择性裂解和高通量的下一代测序,作为定量表征PT修饰的基因组格局的手段。使用PT-IC-seq,我们发现大多数PT位点在E中以较低的PT频率(<5%)被部分修饰。大肠杆菌B7A和小肠沙门氏菌血清Cerro 87,都表现出与典型甲基化修饰相似的PT修饰异质性模式。结合碘诱导的裂解和液滴数字PCR的绝对定量,我们开发了PT-IC-ddPCR技术来进一步测量PT修饰水平。与PT-IC-seq测量一致,PT-IC-ddPCR分析证实E中的PT频率较低。大肠杆菌B7A。我们的研究证明了细菌群体中PT修饰的异质性,并且我们还建立了在整个基因组水平上对PT修饰事件进行严格定位和表征的通用工具。我们以我们的知识描述了PT景观的第一个全基因组定量表征,并为PT修饰的进一步功能研究提供了适当的策略。作者摘要硫代磷酸酯(PT)修饰是一种新颖的DNA修饰,以前的研究表明PT修饰在E中。大肠埃希菌出现在G_(ps)AAC / G_(ps)TTC基序,但每个位点的修饰频率未知。在这项研究中,我们介绍了两种方法:PT-IC-seq,它可以定量表征PT修饰的基因组格局。 PT-IC-ddPCR,可以精确测量PT修饰频率。通过这两种新方法,可以直观,准确地揭示异质性(PT修饰的重要特征)。这项研究中揭示的修饰为PT的生理功能的最终揭示提供了基础,并为其他DNA修饰研究提供了有价值的参考。

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