DNA Phosphorothioate Modification Systems and Associated Phage Defense Systems.

Annu Rev Microbiol

Department of Gastroenterology, Hubei Clinical Center and Key Laboratory of Intestinal and Colorectal Disease, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan, China.

Published: November 2024

AI Article Synopsis

  • DNA phosphorothioate (PT) modification involves replacing a non-bridging oxygen in the DNA sugar-phosphate backbone with sulfur, enhancing the DNA’s resistance to degradation by nucleases.
  • Recent studies have uncovered the roles of PT modification enzymes and their functions across bacterial genomes, notably in distinguishing self DNA from foreign DNA to prevent autoimmunity.
  • The article also discusses potential applications of PT systems, such as creating phage-resistant bacteria, RNA editing, and improving methods for nucleic acid detection.

Article Abstract

In contrast to the well-known DNA methylation of nucleobases, DNA phosphorothioate (PT) modification occurs in the DNA sugar-phosphate backbone. The non-bridging oxygen is replaced by a sulfur atom, which increases the nuclease tolerance of the DNA. In recent years, we have witnessed advances in understanding of PT modification enzymes, the features of PT modification across prokaryotic genomes, and PT-related physiological functions. Although only a small fraction of modifiable recognition sites across bacterial genomes undergo PT modification, enzymes such as DndFGH and SspE can use this modification as a recognition marker to differentiate between self- and non-self-DNA, thus destroying PT-lacking invasive DNA and preventing autoimmunity. We highlight the molecular mechanisms of PT modification-associated defense systems. We also describe notable applications of PT systems in the engineering of phage-resistant bacterial strains, RNA editing, and nucleic acid detection.

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Source
http://dx.doi.org/10.1146/annurev-micro-041222-014330DOI Listing

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