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Genometrics as an essential tool for the assembly of whole genome sequences: the example of the chromosome of Bifidobacterium longum NCC2705

机译:基因组学作为组装全基因组序列的必要工具:长双歧杆菌NCC2705的染色体示例

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Analysis of the first reported complete genome sequence of Bifidobacterium longum NCC2705, an actinobacterium colonizing the gastrointestinal tract, uncovered its proteomic relatedness to Streptomyces coelicolor and Mycobacterium tuberculosis. However, a rapid scrutiny by genometric methods revealed a genome organization totally different from all so far sequenced high-GC Gram-positive chromosomes. Generally, the cumulative GC- and ORF orientation skew curves of prokaryotic genomes consist of two linear segments of opposite slope: the minimum and the maximum of the curves correspond to the origin and the terminus of chromosome replication, respectively. However, analyses of the B. longum NCC2705 chromosome yielded six, instead of two, linear segments, while its dnaA locus, usually associated with the origin of replication, was not located at the minimum of the curves. Furthermore, the coorientation of gene transcription with replication was very low. Comparison with closely related actinobacteria strongly suggested that the chromosome of B. longum was misassembled, and the identification of two pairs of relatively long homologous DNA sequences offers the possibility for an alternative genome assembly proposed here below. By genometric criteria, this configuration displays all of the characters common to bacteria, in particular to related high-GC Gram-positives. In addition, it is compatible with the partially sequenced genome of DJO10A B. longum strain. Recently, a corrected sequence of B. longum NCC2705, with a configuration similar to the one proposed here below, has been deposited in GenBank, confirming our predictions. Genometric analyses, in conjunction with standard bioinformatic tools and knowledge of bacterial chromosome architecture, represent fast and straightforward methods for the evaluation of chromosome assembly.
机译:对最早报道的长双歧杆菌NCC2705(在胃肠道定殖的放线杆菌)的完整基因组序列进行分析,发现其与结肠链霉菌和结核分枝杆菌的蛋白质组学相关性。然而,通过基因组方法的快速审查显示,与迄今为止所有已测序的高GC革兰氏阳性染色体完全不同的基因组组织。通常,原核基因组的累积GC方向和ORF方向偏斜曲线由两个斜率相反的线性段组成:曲线的最小值和最大值分别对应于染色体复制的起点和终点。但是,对长双歧杆菌NCC2705染色体的分析产生了六个而不是两个线性段,而通常与复制起点相关的dnaA位点并未位于曲线的最小值。此外,基因转录与复制的相关性非常低。与密切相关的放线菌的比较强烈表明长双歧杆菌的染色体是错误组装的,并且鉴定两对相对较长的同源DNA序列为下文提出的另一种基因组组装提供了可能性。根据基因组标准,这种构型显示了细菌共有的所有特征,特别是相关的高GC革兰氏阳性菌。另外,它与DJO10A长双歧杆菌菌株的部分测序的基因组相容。最近,已将经校正的长双歧杆菌NCC2705序列(其结构与以下此处提出的结构相似)存放在GenBank中,证实了我们的预测。基因组分析与标准生物信息学工具和细菌染色体结构知识一起,代表了评估染色体装配的快速而直接的方法。

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