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Wavelet Analysis of DNA Bending Profiles reveals Structural Constraints on the Evolution of Genomic Sequences

机译:DNA弯曲曲线的小波分析揭示了基因组序列进化的结构约束

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Analyses of genomic DNA sequences have shown in previous works that base pairs are correlated at large distances with scale-invariant statistical properties. We show in the present study that these correlations between nucleotides (letters) result in fact from long-range correlations (LRC) between sequence-dependent DNA structural elements (words) involved in the packaging of DNA in chromatin. Using the wavelet transform technique, we perform a comparative analysis of the DNA text and of the corresponding bending profiles generated with curvature tables based on nucleosome positioning data. This exploration through the optics of the so-called `wavelet transform microscope' reveals a characteristic scale of 100-200 bp that separates two regimes of different LRC. We focus here on the existence of LRC in the small-scale regime (≲ 200 bp). Analysis of genomes in the three kingdoms reveals that this regime is specifically associated to the presence of nucleosomes. Indeed, small scale LRC are observed in eukaryotic genomes and to a less extent in archaeal genomes, in contrast with their absence in eubacterial genomes. Similarly, this regime is observed in eukaryotic but not in bacterial viral DNA genomes. There is one exception for genomes of Poxviruses, the only animal DNA viruses that do not replicate in the cell nucleus and do not present small scale LRC. Furthermore, no small scale LRC are detected in the genomes of all examined RNA viruses, with one exception in the case of retroviruses. Altogether, these results strongly suggest that small-scale LRC are a signature of the nucleosomal structure. Finally, we discuss possible interpretations of these small-scale LRC in terms of the mechanisms that govern the positioning, the stability and the dynamics of the nucleosomes along the DNA chain. This paper is maily devoted to a pedagogical presentation of the theoretical concepts and physical methods which are well suited to perform a statistical analysis of genomic sequences. We review the results obtained with the so-called wavelet-based multifractal analysis when investigating the DNA sequences of various organisms in the three kingdoms. Some of these results have been announced in B. Audit et al. [1, 2].
机译:对基因组DNA序列的分析在以前的工作中已经表明,碱基对在很长的距离内与尺度不变的统计特性相关。我们在本研究中显示,核苷酸之间的这些相关性(字母)实际上是由参与染色质中DNA包装的序列依赖性DNA结构元件(单词)之间的长期相关性(LRC)引起的。使用小波变换技术,我们对DNA文本和基于核小体定位数据的曲率表生成的相应弯曲轮廓进行了比较分析。通过所谓的“小波变换显微镜”的光学原理进行的探索揭示了一个100-200 bp的特征范围,该特征范围将不同的LRC的两个方案分开。在这里,我们将重点放在LRC在小规模机制(≲200 bp)中的存在。三个王国的基因组分析表明,这种机制与核小体的存在特别相关。实际上,与真细菌基因组中不存在的相比,在真核基因组中观察到了小规模的LRC,而在古细菌基因组中观察到的程度较小。同样,这种机制在真核生物中观察到,但在细菌病毒DNA基因组中未观察到。痘病毒的基因组有一个例外,即唯一的不能在细胞核中复制且不存在小规模LRC的动物DNA病毒。此外,在所有检查的RNA病毒的基因组中均未检测到小规模的LRC,只有逆转录病毒例外。总而言之,这些结果强烈表明小规模的LRC是核小体结构的标志。最后,我们根据控制沿着DNA链的核小体的定位,稳定性和动力学的机制,讨论了这些小型LRC的可能解释。本文主要介绍了理论概念和物理方法的教学法,非常适合对基因组序列进行统计分析。在调查三个王国中各种生物的DNA序列时,我们回顾了通过所谓的基于小波的多重分形分析获得的结果。其中一些结果已在B. Audit等人中宣布。 [1,2]。

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