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Novel heterologous bacterial system reveals enhanced susceptibility to DNA damage mediated by yqgF, a nearly ubiquitous and often essential gene

机译:新型异源细菌系统揭示了由yqgF介导的DNA损伤的敏感性增强,yqgF是近乎普遍存在且通常必不可少的基因

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Despite its presence in most bacteria, yqgF remains one of only 13 essential genes of unknown function in Escherichia coli. Predictions of YqgF function often derive from sequence similarity to RuvC, the canonical Holliday junction resolvase. To clarify its role, we deleted yqgF from a bacterium where it is not essential, Acinetobacter baylyi ADP1. Loss of yqgF impaired growth and increased the frequency of transformation and allelic replacement (TAR). When E. coli yqgF was inserted in place of its A. baylyi chromosomal orthologue, wild-type growth and TAR were restored. Functional similarities of yqgF in both gamma-proteobacteria were further supported by defective 16S rRNA processing by the A. baylyi mutant, an effect previously shown in E. coli for a temperature-sensitive yqgF allele. However, our data question the validity of deducing YqgF function strictly by comparison to RuvC. A. baylyi studies indicated that YqgF and RuvC can function in opposition to one another. Relative to the wild type, the ΔyqgF mutant had increased TAR frequency and increased resistance to nalidixic acid, a DNA-damaging agent. In contrast, deletion of ruvC decreased TAR frequency and lowered resistance to nalidixic acid. YqgF, but not RuvC, appears to increase bacterial susceptibility to DNA damage, including UV radiation. Nevertheless, the effects of yqgF on growth and TAR frequency were found to depend on amino acids analogous to catalytically required residues of RuvC. This new heterologous system should facilitate future yqgF investigation by exploiting the viability of A. baylyi yqgF mutants. In addition, bioinformatic analysis showed that a non-essential gene immediately upstream of yqgF in A. baylyi and E. coli (yqgE) is similarly positioned in most gamma- and beta-proteobacteria. A small overlap in the coding sequences of these adjacent genes is typical. This conserved genetic arrangement raises the possibility of a functional partnership between yqgE and yqgF.
机译:尽管存在于大多数细菌中,yqgF仍然是大肠杆菌中仅有的13个功能未知的必需基因之一。对YqgF功能的预测通常源自与RuvC(规范的霍利迪连接酶)的序列相似性。为了阐明其作用,我们从并非必需的细菌(不动杆菌Baylyi ADP1)中删除了yqgF。 yqgF的丧失会损害生长,并增加转化和等位基因置换(TAR)的频率。当插入大肠杆菌yqgF代替其A. baylyi染色体直向同源物时,野生型生长和TAR被恢复。两种γ-变形杆菌中yqgF的功能相似性都受到Baylyi突变体对16S rRNA加工的缺陷的支持,这种作用先前已在大肠杆菌中显示为对温度敏感的yqgF等位基因。但是,我们的数据与RuvC相比,严格地推论YqgF函数的有效性。 A. baylyi研究表明,YqgF和RuvC可以相互对抗。相对于野生型,ΔyqgF突变体具有更高的TAR频率和对DNA破坏剂萘啶酸的抗性。相反,ruvC的缺失降低了TAR频率并降低了对萘啶酸的抗性。 YqgF而非RuvC似乎增加了细菌对DNA损伤(包括紫外线)的敏感性。尽管如此,发现yqgF对生长和TAR频率的影响取决于类似于RuvC催化所需残基的氨基酸。这种新的异源系统应通过利用A. baylyi yqgF突变体的生存力来促进未来yqgF的研究。此外,生物信息学分析表明,在A.baylyi和大肠杆菌(yqgE)中紧接yqgF上游的一个非必需基因在大多数γ-和β-蛋白菌中也有类似的定位。这些相邻基因的编码序列中通常有很小的重叠。这种保守的遗传安排提高了yqgE和yqgF之间功能性伙伴关系的可能性。

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