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Comparative Analysis of Sequence Periodicity among Prokaryotic Genomes Points to Differences in Nucleoid Structure and a Relationship to Gene Expression

机译:原核基因组中序列周期性的比较分析指出核样结构的差异及其与基因表达的关系

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摘要

Regular spacing of short runs of A or T nucleotides in DNA sequences with a period close to the helical period of the DNA double helix has been associated with intrinsic DNA bending and nucleosome positioning in eukaryotes. Analogous periodic signals were also observed in prokaryotic genomes. While the exact role of this periodicity in prokaryotes is not known, it has been proposed to facilitate the DNA packaging in the prokaryotic nucleoid and/or to promote negative or positive supercoiling. We developed a methodology for assessments of intragenomic heterogeneity of these periodic patterns and applied it in analysis of 1,025 prokaryotic chromosomes. This technique allows more detailed analysis of sequence periodicity than previous methods where sequence periodicity was assessed in an integral form across the whole chromosome. We found that most genomes have the periodic signal confined to several chromosomal segments while most of the chromosome lacks a strong sequence periodicity. Moreover, there are significant differences among different prokaryotes in both the intensity and persistency of sequence periodicity related to DNA curvature. We proffer that the prokaryotic nucleoid consists of relatively rigid sections stabilized by short intrinsically bent DNA segments and characterized by locally strong periodic patterns alternating with regions featuring a weak periodic signal, which presumably permits higher structural flexibility. This model applies to most bacteria and archaea. In genomes with an exceptionally persistent periodic signal, highly expressed genes tend to concentrate in aperiodic sections, suggesting that structural heterogeneity of the nucleoid is related to local differences in transcriptional activity.
机译:DNA序列中A或T核苷酸短周期的规则间隔(接近DNA双螺旋的螺旋周期)与真核生物中固有的DNA弯曲和核小体定位有关。在原核基因组中也观察到类似的周期性信号。虽然该周期在原核生物中的确切作用尚不清楚,但已提出促进DNA包装在原核生物核苷酸中和/或促进负或正超螺旋。我们开发了一种评估这些周期性模式的基因组内异质性的方法,并将其应用于分析1,025个原核染色体。与以前的方法相比,此技术可以对序列周期性进行更详细的分析,在以前的方法中,以完整的形式评估整个染色体的序列周期性。我们发现,大多数基因组的周期信号都局限于几个染色体片段,而大多数染色体却缺乏很强的序列周期性。而且,在与DNA曲率有关的序列周期性的强度和持久性上,不同原核生物之间存在显着差异。我们推测原核生物核苷酸由相对较短的部分组成,该部分由较短的固有弯曲的DNA片段稳定,并具有局部强周期性模式和周期性弱信号区域,可能具有较高的结构灵活性。此模型适用于大多数细菌和古细菌。在具有异常持久的周期性信号的基因组中,高表达的基因倾向于集中在非周期性切片中,这表明核苷的结构异质性与转录活性的局部差异有关。

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