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Where does bacterial replication start? Rules for predicting the oriC region

机译:细菌复制从哪里开始?预测oriC区域的规则

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Three methods, based on DNA asymmetry, the distribution of DnaA boxes and dnaA gene location, were applied to identify the putative replication origins in 120 chromosomes. The chromosomes were classified according to the agreement of these methods and the applicability of these methods was evaluated. DNA asymmetry is the most universal method of putative oriC identification in bacterial chromosomes, but it should be applied together with other methods to achieve better prediction. The three methods identify the same region as a putative origin in all Bacilli and Clostridia, many Actinobacteria and γ Proteobacteria. The organization of clusters of DnaA boxes was analysed in detail. For 76 chromosomes, a DNA fragment containing multiple DnaA boxes was identified as a putative origin region. Most bacterial chromosomes exhibit an overrepresentation of DnaA boxes; many of them contain at least two clusters of DnaA boxes in the vicinity of the oriC region. The additional clusters of DnaA boxes are probably involved in controlling replication initiation. Surprisingly, the characteristic features of the initiation of replication, i.e. a cluster of DnaA boxes, a dnaA gene and a switch in asymmetry, were not found in some of the analysed chromosomes, particularly those of obligatory intracellular parasites or endosymbionts. This is presumably connected with many mechanisms disturbing DNA asymmetry, translocation or disappearance of the dnaA gene and decay of the Escherichia coli perfect DnaA box pattern.
机译:基于DNA不对称性,DnaA盒的分布和dnaA基因位置的三种方法,被用于鉴定120条染色体中假定的复制起点。根据这些方法的一致性对染色体进行分类,并评估这些方法的适用性。 DNA不对称是细菌染色体中最普遍的oriC鉴定方法,但应与其他方法结合使用以实现更好的预测。这三种方法在所有杆菌和梭状芽胞杆菌,许多放线菌和γ变形杆菌中都将相同的区域确定为推定来源。详细分析了DnaA盒簇的组织。对于76条染色体,包含多个DnaA盒的DNA片段被鉴定为推定的起源区域。大多数细菌染色体表现出过高的DnaA盒表达;其中许多在oriC区域附近至少包含两个DnaA框簇。 DnaA框的其他群集可能参与控制复制启动。出乎意料的是,在某些分析的染色体中,特别是那些必需的细胞内寄生虫或共生菌的染色体中,没有发现复制起始的特征,即一簇DnaA盒,一个dnaA基因和一个不对称开关。据推测,这与干扰DNA不对称性,dnaA基因的易位或消失以及大肠杆菌完美DnaA盒型的衰退的许多机制有关。

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