Genome editing outcomes reveal mycobacterial NucS participates in a short-patch repair of DNA mismatches.
Tanjina IslamEric A JosephsPublished in: Nucleic acids research (2024)
In the canonical DNA mismatch repair (MMR) mechanism in bacteria, if a nucleotide is incorrectly mis-paired with the template strand during replication, the resulting repair of this mis-pair can result in the degradation and re-synthesis of hundreds or thousands of nucleotides on the newly-replicated strand (long-patch repair). While mycobacteria, which include important pathogens such as Mycobacterium tuberculosis, lack the otherwise highly-conserved enzymes required for the canonical MMR reaction, it was found that disruption of a mycobacterial mismatch-sensitive endonuclease NucS results in a hyper-mutative phenotype, leading to the idea that NucS might be involved in a cryptic, independently-evolved DNA MMR mechanism, perhaps mediated by homologous recombination (HR) with a sister chromatid. Using oligonucleotide recombination, which allows us to introduce mismatches specifically into the genomes of a model for M. tuberculosis, Mycobacterium smegmatis, we find that NucS participates in a direct repair of DNA mismatches where the patch of excised nucleotides is largely confined to within ∼5-6 bp of the mis-paired nucleotides, which is inconsistent with mechanistic models of canonical mycobacterial HR or other double-strand break (DSB) repair reactions. The results presented provide evidence of a novel NucS-associated mycobacterial MMR mechanism occurring in vivo to regulate genetic mutations in mycobacteria.
Keyphrases
- mycobacterium tuberculosis
- circulating tumor
- dna repair
- genome editing
- cell free
- single molecule
- pulmonary tuberculosis
- crispr cas
- dna damage
- genome wide
- transcription factor
- emergency department
- nucleic acid
- gene expression
- type diabetes
- metabolic syndrome
- dna methylation
- insulin resistance
- single cell
- hiv infected
- drug induced