Maurer Sandy, Ludt Katharina, Soppa Jörg
Goethe University, Institute for Molecular Biosciences, Frankfurt, Germany.
Goethe University, Institute for Molecular Biosciences, Frankfurt, Germany
J Bacteriol. 2017 Dec 5;200(1). doi: 10.1128/JB.00517-17. Print 2018 Jan 1.
is polyploid and contains about 20 genome copies under optimal conditions. However, the chromosome copy number is highly regulated and ranges from two during phosphate starvation to more than 40 under conditions of phosphate surplus. The aim of this study was the characterization of the influence of two replication origins on the genome copy number. The origin repeats and the genes encoding rigin ecognition omplex (ORC) proteins were deleted. The core origin oriC1- (ori1) deletion mutant had a lower genome copy number and a higher level of fitness than the wild type, in stark contrast to the oriC2- (ori2) deletion mutant. The genes adjacent to ori1 could not be deleted, and thus, at least two of them are probably essential, while deletion of the genes adjacent to ori2 was possible. Various fragments of and around the origins were cloned into a suicide plasmid to generate aloarchaeal rtificial hromosomes (HACs). The copy number of the oriC1- HAC was much higher than that of the oriC2- HAC. The addition of adjacent genes influenced both the HAC copy number and the chromosome copy number. The results indicate that the origins of are not independent but that the copy number is regulated via a network of genes around the origins. Several species of archaea have more than one origin of replication on their major chromosome and are thus the only known prokaryotic species that allow the analysis of the evolution of multiorigin replication. The widely studied H26 strain has a major chromosome with four origins of replication. Two origins, ori1 and ori2, were chosen for an in-depth analysis using deletion mutants and haloarchaeal artificial chromosomes. The analysis was not restricted to the core origin regions; origin-adjacent genes were also included. Because is polyploid, the effects on the chromosome copy number were of specific importance. The results revealed extreme differences between the two origins.
在最佳条件下是多倍体,含有约20个基因组拷贝。然而,染色体拷贝数受到高度调控,在磷酸盐饥饿时为两个,在磷酸盐过剩条件下则超过40个。本研究的目的是表征两个复制起点对基因组拷贝数的影响。删除了起点重复序列和编码起点识别复合体(ORC)蛋白的基因。与野生型形成鲜明对比的是,核心起点oriC1-(ori1)缺失突变体的基因组拷贝数较低,但适应性水平较高,而oriC2-(ori2)缺失突变体则不然。与ori1相邻的基因无法删除,因此其中至少两个可能是必需的,而与ori2相邻的基因则可以删除。将起点及其周围的各种片段克隆到自杀质粒中,以产生嗜盐古菌人工染色体(HACs)。oriC1-HAC的拷贝数远高于oriC2-HAC。相邻基因的添加影响了HAC拷贝数和染色体拷贝数。结果表明,的起点并非独立存在,而是通过起点周围的基因网络来调控拷贝数。几种古菌在其主要染色体上有多个复制起点,因此是唯一已知的允许分析多起点复制进化的原核生物物种。广泛研究的H26菌株有一条带有四个复制起点的主要染色体。选择了两个起点ori1和ori2,使用缺失突变体和嗜盐古菌人工染色体进行深入分析。分析不仅限于核心起点区域,还包括与起点相邻的基因。由于是多倍体,对染色体拷贝数的影响具有特殊重要性。结果揭示了两个起点之间的极端差异。