4.8 Article

The complex methylome of the human gastric pathogen Helicobacter pylori

期刊

NUCLEIC ACIDS RESEARCH
卷 42, 期 4, 页码 2415-2432

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt1201

关键词

-

资金

  1. German Research Foundation (DFG) [DFG SFB 900/A1, DFG SFB 900/Z1, DFG SFB 900/B6]
  2. BMBF (HELDIVPAT)
  3. German Center of Infection Research (DZIF) [8000-105-3]
  4. NIH [1R44GM105125, 1R44GM100560]
  5. DFG

向作者/读者索取更多资源

The genome of Helicobacter pylori is remarkable for its large number of restriction-modification (R-M) systems, and strain-specific diversity in R-M systems has been suggested to limit natural transformation, the major driving force of genetic diversification in H. pylori. We have determined the comprehensive methylomes of two H. pylori strains at single base resolution, using Single Molecule Real-Time (SMRT (R)) sequencing. For strains 26695 and J99-R3, 17 and 22 methylated sequence motifs were identified, respectively. For most motifs, almost all sites occurring in the genome were detected as methylated. Twelve novel methylation patterns corresponding to nine recognition sequences were detected (26695, 3; J99-R3, 6). Functional inactivation, correction of frameshifts as well as cloning and expression of candidate methyltransferases (MTases) permitted not only the functional characterization of multiple, yet undescribed, MTases, but also revealed novel features of both Type I and Type II R-M systems, including frameshift-mediated changes of sequence specificity and the interaction of one MTase with two alternative specificity subunits resulting in different methylation patterns. The methylomes of these well-characterized H. pylori strains will provide a valuable resource for future studies investigating the role of H. pylori R-M systems in limiting transformation as well as in gene regulation and host interaction.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据