Either non-homologous ends joining or homologous recombination is required to repair double-strand breaks in the genome of macrophage-internalized Mycobacterium tuberculosis.
The intracellular pathogen Mycobacterium tuberculosis (Mtb) is constantly exposed to a multitude of hostile conditions and is confronted by a variety of potentially DNA-damaging assaults in vivo, primarily from host-generated antimicrobial toxic radicals. Exposure to reactive nitrogen species and/or...
Main Authors: | Anna Brzostek, Izabela Szulc, Magdalena Klink, Marta Brzezinska, Zofia Sulowska, Jaroslaw Dziadek |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2014-01-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24658131/?tool=EBI |
Similar Items
-
Cholesterol oxidase is indispensable in the pathogenesis of Mycobacterium tuberculosis.
by: Magdalena Klink, et al.
Published: (2013-01-01) -
The efficiency of homologous recombination and non-homologous end joining systems in repairing double-strand breaks during cell cycle progression.
by: Leonardo Bee, et al.
Published: (2013-01-01) -
IGF-1R inhibition enhances radiosensitivity and delays double-strand break repair by both non-homologous end-joining and homologous recombination.
by: Chitnis, M, et al.
Published: (2014) -
Telomere-Internal Double-Strand Breaks Are Repaired by Homologous Recombination and PARP1/Lig3-Dependent End-Joining
by: Ylli Doksani, et al.
Published: (2016-11-01) -
Non-Homologous End Joining and Homology Directed DNA Repair Frequency of Double-Stranded Breaks Introduced by Genome Editing Reagents.
by: Michail Zaboikin, et al.
Published: (2017-01-01)