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Sequence periodicity in nucleosomal DNA and intrinsic curvature

机译:核小体DNA中的序列周期性和固有曲率

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BackgroundMost eukaryotic DNA contained in the nucleus is packaged by wrapping DNA around histone octamers. Histones are ubiquitous and bind most regions of chromosomal DNA. In order to achieve smooth wrapping of the DNA around the histone octamer, the DNA duplex should be able to deform and should possess intrinsic curvature. The deformability of DNA is a result of the non-parallelness of base pair stacks. The stacking interaction between base pairs is sequence dependent. The higher the stacking energy the more rigid the DNA helix, thus it is natural to expect that sequences that are involved in wrapping around the histone octamer should be unstacked and possess intrinsic curvature. Intrinsic curvature has been shown to be dictated by the periodic recurrence of certain dinucleotides. Several genome-wide studies directed towards mapping of nucleosome positions have revealed periodicity associated with certain stretches of sequences. In the current study, these sequences have been analyzed with a view to understand their sequence-dependent structures.ResultsHigher order DNA structures and the distribution of molecular bend loci associated with 146 base nucleosome core DNA sequence from C. elegans and chicken have been analyzed using the theoretical model for DNA curvature. The curvature dispersion calculated by cyclically permuting the sequences revealed that the molecular bend loci were delocalized throughout the nucleosome core region and had varying degrees of intrinsic curvature.ConclusionsThe higher order structures associated with nucleosomes of C.elegans and chicken calculated from the sequences revealed heterogeneity with respect to the deviation of the DNA axis. The results points to the possibility of context dependent curvature of varying degrees to be associated with nucleosomal DNA.
机译:背景技术通过将DNA包裹在组蛋白八聚体周围来包装细胞核中包含的大多数真核DNA。组蛋白无处不在,并结合染色体DNA的大多数区域。为了在组蛋白八聚体周围实现DNA的平滑包裹,DNA双链体应能够变形并具有固有的曲率。 DNA的可变形性是碱基对堆栈不平行的结果。碱基对之间的堆叠相互作用是序列依赖性的。堆积能量越高,DNA螺旋越硬,因此自然可以预期包裹在组蛋白八聚体周围的序列应该是未堆积的并具有固有曲率。固有曲率已被证明是由某些二核苷酸的周期性复发决定的。几项针对核小体位置作图的全基因组研究表明,与某些序列片段相关的周期性。在当前的研究中,已经对这些序列进行了分析,以了解它们的序列依赖性结构。结果使用C. elegans和鸡分析了与146个碱基核小体核心DNA序列相关的高阶DNA结构和分子弯曲位点的分布。 DNA曲率的理论模型。循环排列序列的曲率分散表明分子弯曲位点在整个核小体核心区域内是不集中的,并且具有不同程度的固有曲率。结论根据序列计算的与秀丽隐杆线虫和鸡核小体相关的高阶结构显示出异质性。关于DNA轴的偏差。结果表明,与上下文相关的不同程度的曲率可能与核小体DNA相关。

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