4.5 Article

Identification of the DNA methyltransferases establishing the methylome of the cyanobacterium Synechocystis sp PCC 6803

期刊

DNA RESEARCH
卷 25, 期 4, 页码 343-352

出版社

OXFORD UNIV PRESS
DOI: 10.1093/dnares/dsy006

关键词

cyanobacteria; DNA methyltransferase; mutant; photosynthetic pigment; phylogenetics

资金

  1. German Research Foundation (Deutsche Forschungsgemeinschaft) [HA2002/17-1, HE 2544/10-1]

向作者/读者索取更多资源

DNA methylation in bacteria is important for defense against foreign DNA, but is also involved in DNA repair, replication, chromosome partitioning, and regulatory processes. Thus, characterization of the underlying DNA methyltransferases in genetically tractable bacteria is of paramount importance. Here, we characterized the methylome and orphan methyltransferases in the model cyanobacterium Synechocystis sp. PCC 6803. Single molecule real-time ( SMRT) sequencing revealed four DNA methylation recognition sequences in addition to the previously known motif (m5)CGATCG, which is recognized by M.Ssp6803I. For three of the new recognition sequences, we identified the responsible methyltransferases. M.Ssp6803II, encoded by the sll0729 gene, modifies GG(m4)CC, M.Ssp6803III, encoded by slr1803, represents the cyanobacterial dam-like methyltransferase modifying G(m6)ATC, and M.Ssp6803V, encoded by slr6095 on plasmid pSYSX, transfers methyl groups to the bipartite motif GG(m6)AN(7)TTGG/CCA(m6)AN(7)TCC. The remaining methylation recognition sequence GA(m6)AGGC is probably recognized by methyltransferase M.Ssp6803IV encoded by slr6050. M.Ssp6803III and M.Ssp6803IV were essential for the viability of Synechocystis, while the strains lacking M.Ssp6803III and M.Ssp6803V showed growth similar to the wild type. In contrast, growth was strongly diminished of the Delta sll0729 mutant lacking M.Ssp6803II. These data provide the basis for systematic studies on the molecular mechanisms impacted by these methyltransferases.

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

4.5
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