大肠杆菌基因组前后链重复序列的分布:长直接重复序列(LDR)序列的比较研究。

M. Kawano, S. Kanaya, T. Oshima, Yasushi Masuda, T. Ara, H. Mori
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引用次数: 11

摘要

在本研究中,我们开发了一种检测与目标序列相似度具有统计学意义的序列的方法,并检查了这些序列在大肠杆菌K-12基因组中的分布。检测的靶序列如下:(i)短重复序列:交叉热点启动序列(Chi)、复制终止序列(Ter)和dna结合序列(DnaA box);(ii)潜在的茎环结构重复序列:回文单位(PU)、boxC序列和基因间重复单位(IRU);(iii)潜在的RNA编码重复序列:rnas、PAIR、TRIP和QUAD;(iv)潜在的蛋白质编码重复序列:插入元件(ISs)和长直接重复序列(LDRs)。我们还研究了这些序列在前导链和滞后链上的分布。我们在LDR位点附近获得了另外4个具有统计学意义的LDR序列,它们与LDR- a的匹配值超过187bp,这表明这些区域可能是LDR的高重组热点。根据密码子的使用,还讨论了单个ldr对大肠杆菌基因组的适应性。
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Distribution of repetitive sequences on the leading and lagging strands of the Escherichia coli genome: comparative study of Long Direct Repeat (LDR) sequences.
In the present study, we developed a method for detecting sequences whose similarity to a target sequence is statistically significant and we examined the distribution of these sequences in the E. coli K-12 genome. Target sequences examined are as follows: (i) short repeat: Crossover hot-spot instigator (Chi) sequence, replication termination (Ter) sequence, and DnaA binding sequence (DnaA box); (ii) potential stem-loop structure repeats: palindromic unit (PU), boxC sequences, and intergenic repeat unit (IRU); (iii) potential RNA coding repeats: rRNAs, PAIR, TRIP, and QUAD; and (iv) potential protein coding repeats: insertion elements (ISs) and Long Direct Repeats (LDRs). We also examined the distribution of these sequences on leading and lagging strands. We obtained another four statistically significant LDR sequences with more than 187 bp matched to LDR-A near the LDR loci, suggesting that these regions might be used as high recombination hot spots for LDR. Adaptation of individual LDRs to E. coli genome is also discussed on the basis of codon usage.
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