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BREX system of Escherichia coli distinguishes self from non-self by methylation of a specific DNA site
- Source :
- Nucleic acids research, Oxford : Oxford University Press, 2019, vol. 47, iss. 1, p. 253-265, Nucleic Acids Research
- Publication Year :
- 2019
-
Abstract
- Prokaryotes evolved numerous systems that defend against predation by bacteriophages. In addition to well-known restriction-modification and CRISPR-Cas immunity systems, many poorly characterized systems exist. One class of such systems, named BREX, consists of a putative phosphatase, a methyltransferase and four other proteins. A Bacillus cereus BREX system provides resistance to several unrelated phages and leads to modification of specific motif in host DNA. Here, we study the action of BREX system from a natural Escherichia coli isolate. We show that while it makes cells resistant to phage λ infection, induction of λ prophage from cells carrying BREX leads to production of viruses that overcome the defense. The induced phage DNA contains a methylated adenine residue in a specific motif. The same modification is found in the genome of BREX-carrying cells. The results establish, for the first time, that immunity to BREX system defense is provided by an epigenetic modification.
- Subjects :
- BREX system
methylation
CRISPR-Cas
Biology
medicine.disease_cause
Genome
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Plasmid
Bacillus cereus
Genetics
medicine
Escherichia coli
Epigenetics
Nucleotide Motifs
Gene
Molecular Biology
Prophage
030304 developmental biology
0303 health sciences
Adenine
Methylation
Methyltransferases
DNA Methylation
Bacteriophage lambda
Phosphoric Monoester Hydrolases
3. Good health
chemistry
CRISPR-Cas Systems
030217 neurology & neurosurgery
DNA
Subjects
Details
- Language :
- English
- ISSN :
- 03051048 and 13624962
- Database :
- OpenAIRE
- Journal :
- Nucleic acids research, Oxford : Oxford University Press, 2019, vol. 47, iss. 1, p. 253-265, Nucleic Acids Research
- Accession number :
- edsair.doi.dedup.....2b479f27d9f43e11b6b4edb3932d7a0b