基于集成多平台定位数据的酵母基因组核小体组装位置槽模型

Jihua Feng, X. Dai, Qian Xiang, Zhiming Dai, Jiang-Hai Wang, Yangyang Deng, Caisheng He
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引用次数: 0

摘要

对最近五个实验核小体数据集的深入分析揭示了以前研究中检测到的最终核小体位置之间的广泛分歧。利用信号处理方法,我们发现了两个不同的核小体分布域,它们明显出现在启动子区和编码区。我们计算并证实,模糊核小体属于动态结构域,定位良好的核小体属于稳定结构域。通过将结构域信息与基因特性、转录因子结合位点(TFBs)和DNA可弯曲性相结合,我们揭示了这两个结构域与TATA和TATA_less基因之间的关系。然后,研究这两个结构域与组蛋白H3修饰之间的联系,我们观察到极快替换的组蛋白H3发生在转录起始位点(TSS)的直接下游,而不是+1核小体位置。最后,我们提出了酵母基因组核小体组装的槽模型来解释核小体在基因启动子区域形成的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A position-slots model for nucleosome assembly in the yeast genome based on integrated multi-platform positioning dataseis
In-depth analysis of the recent five experimental nucleosome datasets reveals the broad disagreements between the final nucleosome positions detected by the previous studies. Using signal processing methods, we found two distinct nucleosome distribution domains which evidently emerge from promoter and coding regions. We calculated and confirmed that the fuzzy nucleosomes fall into the dynamic domain, and well-positioned nucleosomes fall into the stable one. By combining the domains information with gene properties, transcription factors binding sites (TFBs) and DNA bendability, we revealed the relationship between the two domains with TATA and TATA_less genes. Then, investigating the link between the two domains and the histone H3 modifications, we observed that the extremely rapid-replacing histone H3 occurs at the immediate downstream of transcription start sites (TSS) rather than +1 nucleosome position. Finally, we presented a slots model for nucleosome assembly in the yeast genome to explain the mechanism of nucleosome forming in the genes promoter regions.
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