生物
突变体
支原体
干燥
非同源性末端接合
野生型
DNA修复
DNA
同源重组
遗传学
植物
基因
结核分枝杆菌
医学
肺结核
病理
作者
R. S. Pitcher,Andrew J. Green,Anna Brzostek,Małgorzata Korycka-Machała,Jarosław Dziadek,Aidan J. Doherty
出处
期刊:DNA Repair
[Elsevier]
日期:2007-09-01
卷期号:6 (9): 1271-1276
被引量:82
标识
DOI:10.1016/j.dnarep.2007.02.009
摘要
The physiological role of the non-homologous end-joining (NHEJ) pathway in the repair of DNA double-strand breaks (DSBs) was examined in Mycobacterium smegmatis using DNA repair mutants (DeltarecA, Deltaku, DeltaligD, Deltaku/ligD, DeltarecA/ku/ligD). Wild-type and mutant strains were exposed to a range of doses of ionizing radiation at specific points in their life-cycle. NHEJ-mutant strains (Deltaku, DeltaligD, Deltaku/ligD) were significantly more sensitive to ionizing radiation (IR) during stationary phase than wild-type M. smegmatis. However, there was little difference in IR sensitivity between NHEJ-mutant and wild-type strains in logarithmic phase. Similarly, NHEJ-mutant strains were more sensitive to prolonged desiccation than wild-type M. smegmatis. A DeltarecA mutant strain was more sensitive to desiccation and IR during both stationary and especially in logarithmic phase, compared to wild-type strain, but it was significantly less sensitive to IR than the DeltarecA/ku/ligD triple mutant during stationary phase. These data suggest that NHEJ and homologous recombination are the preferred DSB repair pathways employed by M. smegmatis during stationary and logarithmic phases, respectively.
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