State Key Laboratory of Bioelectronics, Southeast University, Nanjing 210096, China.
BMC Genomics. 2011 Jan 27;12:72. doi: 10.1186/1471-2164-12-72.
Nucleosome positioning has an important role in gene regulation. However, dynamic positioning in vivo casts doubt on the reliability of predictions based on DNA sequence characteristics. What role does sequence-dependent positioning play? In this paper, using a curvature profile model, nucleosomes are predicted in the human genome and patterns of nucleosomes near some key sites are investigated.
Curvature profiling revealed that in the vicinity of a transcription start site, there is also a nucleosome-free region. Near transcription factor binding sites, curvature profiling showed a trough, indicating nucleosome depletion. The trough of the curvature profile corresponds well to the high binding scores of transcription factors. Moreover, our analysis suggests that nucleosome positioning has a selective protection role. Target sites of miRNAs are occupied by nucleosomes, while single nucleotide polymorphism sites are depleted of nucleosomes.
The results indicate that DNA sequences play an important role in nucleosome positioning, and the positioning is important not only in gene regulation, but also in genetic variation and miRNA functions.
核小体定位在基因调控中具有重要作用。然而,体内的动态定位对基于 DNA 序列特征的预测的可靠性提出了质疑。序列依赖性定位扮演什么角色?在本文中,我们使用曲率轮廓模型预测了人类基因组中的核小体,并研究了一些关键位点附近核小体的模式。
曲率分析显示,在转录起始位点附近,也存在无核小体区域。在转录因子结合位点附近,曲率分析显示出一个低谷,表明核小体耗竭。曲率轮廓的低谷与转录因子的高结合分数非常吻合。此外,我们的分析表明核小体定位具有选择性保护作用。miRNA 的靶位点被核小体占据,而单核苷酸多态性位点则缺乏核小体。
结果表明,DNA 序列在核小体定位中起着重要作用,这种定位不仅在基因调控中很重要,而且在遗传变异和 miRNA 功能中也很重要。