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幽门螺杆菌甲基化组:在基因调控和毒力中的作用

The Helicobacter pylori Methylome: Roles in Gene Regulation and Virulence.

作者信息

Gorrell Rebecca, Kwok Terry

机构信息

Infection and Immunity, and Cancer Programs, Monash Biomedicine Discovery Institute, Clayton, Australia.

Department of Biochemistry and Molecular Biology, Monash University, Clayton, 3800, Australia.

出版信息

Curr Top Microbiol Immunol. 2017;400:105-127. doi: 10.1007/978-3-319-50520-6_5.

Abstract

The methylome is defined as a map of DNA methylation patterns at single-base resolution. DNA methylation in bacteria was first discovered as a function of restriction-modification (R-M) systems. R-M systems in Helicobacter pylori, like those in other bacteria, are important host-specificity determinants that provide protection against foreign DNA. Moreover, the gene regulatory role of the methyltransferase (Mtase) unit of various Helicobacter pylori R-M systems is being increasingly recognized. Recent advances in the application of single-molecule real-time (SMRT) DNA sequencing to analyse DNA methylation have revealed for the first time comprehensive pictures of the genome-wide distribution of methylation sites in various strains of H. pylori. The methylomic data published so far have not only confirmed the significant inter-strain diversity of H. pylori Mtases and their DNA methylation profiles, but also identified numerous novel Mtase target recognition sites. The precise knowledge of the nucleotide sequence of Mtase recognition sites and their distribution within the H. pylori genome will in turn enable researchers to more readily test hypotheses on how H. pylori Mtases function to orchestrate gene regulation and/or modulate virulence. Methylomic studies hold promise for providing a deeper understanding into the roles of H. pylori Mtase and R-M systems in the physiology, epigenetics and possibly also pathogenesis of this important human pathogen. Consequently, the knowledge gained will provide crucial insights into the potential application of H. pylori methylomes as novel biomarkers for the prediction of disease outcome and/or antibiotic susceptibility.

摘要

甲基化组被定义为单碱基分辨率下的DNA甲基化模式图谱。细菌中的DNA甲基化最初是作为限制修饰(R-M)系统的一种功能被发现的。幽门螺杆菌中的R-M系统与其他细菌中的一样,是重要的宿主特异性决定因素,可提供对外源DNA的保护。此外,各种幽门螺杆菌R-M系统的甲基转移酶(Mtase)单元的基因调控作用也越来越受到认可。单分子实时(SMRT)DNA测序在分析DNA甲基化方面的最新进展首次揭示了幽门螺杆菌不同菌株中甲基化位点全基因组分布的全貌。迄今为止公布的甲基化组数据不仅证实了幽门螺杆菌Mtase及其DNA甲基化谱在菌株间存在显著差异,还鉴定出了许多新的Mtase靶标识别位点。对Mtase识别位点的核苷酸序列及其在幽门螺杆菌基因组内分布的精确了解,反过来将使研究人员能够更轻松地检验关于幽门螺杆菌Mtase如何发挥作用以协调基因调控和/或调节毒力的假设。甲基化组研究有望更深入地了解幽门螺杆菌Mtase和R-M系统在这种重要人类病原体的生理学、表观遗传学以及可能的发病机制中的作用。因此,所获得的知识将为幽门螺杆菌甲基化组作为预测疾病结局和/或抗生素敏感性的新型生物标志物的潜在应用提供关键见解。

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