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Phosphorothioate DNA modification by BREX Type 4 systems in the human gut microbiome.
Yuan, Yifeng; DeMott, Michael S; Byrne, Shane R; Flores, Katia; Poyet, Mathilde; Groussin, Mathieu; Microbiome Conservancy, Global; Berdy, Brittany; Comstock, Laurie; Alm, Eric J; Dedon, Peter C.
Afiliação
  • Yuan Y; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • DeMott MS; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Byrne SR; Center for Environmental Health Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Flores K; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Poyet M; Department of Microbiology, Duchossois Family Institute, University of Chicago, Chicago, IL, USA.
  • Groussin M; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Microbiome Conservancy G; Institute of Experimental Medicine, Kiel University, Germany.
  • Berdy B; Global Microbiome Conservancy (https://microbiomeconservancy.org/), Kiel University, Germany.
  • Comstock L; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Alm EJ; Institute of Clinical and Molecular Biology, Kiel University, Germany.
  • Dedon PC; Global Microbiome Conservancy (https://microbiomeconservancy.org/), Kiel University, Germany.
bioRxiv ; 2024 Jun 03.
Article em En | MEDLINE | ID: mdl-38895356
ABSTRACT
Among dozens of microbial DNA modifications regulating gene expression and host defense, phosphorothioation (PT) is the only known backbone modification, with sulfur inserted at a non-bridging oxygen by dnd and ssp gene families. Here we explored the distribution of PT genes in 13,663 human gut microbiome genomes, finding that 6.3% possessed dnd or ssp genes predominantly in Bacillota, Bacteroidota, and Pseudomonadota. This analysis uncovered several putative new PT synthesis systems, including Type 4 Bacteriophage Exclusion (BREX) brx genes, which were genetically validated in Bacteroides salyersiae. Mass spectrometric analysis of DNA from 226 gut microbiome isolates possessing dnd, ssp, and brx genes revealed 8 PT dinucleotide settings confirmed in 6 consensus sequences by PT-specific DNA sequencing. Genomic analysis showed PT enrichment in rRNA genes and depletion at gene boundaries. These results illustrate the power of the microbiome for discovering prokaryotic epigenetics and the widespread distribution of oxidation-sensitive PTs in gut microbes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos