Accurate Identification of DNA Replication Origin by Fusing Epigenomics and Chromatin Interaction Information.

IF 10.7
Research (Washington, D.C.) Pub Date : 2022-10-29 eCollection Date: 2022-01-01 DOI:10.34133/2022/9780293
Fu-Ying Dao, Hao Lv, Melissa J Fullwood, Hao Lin
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引用次数: 15

Abstract

DNA replication initiation is a complex process involving various genetic and epigenomic signatures. The correct identification of replication origins (ORIs) could provide important clues for the study of a variety of diseases caused by replication. Here, we design a computational approach named iORI-Epi to recognize ORIs by incorporating epigenome-based features, sequence-based features, and 3D genome-based features. The iORI-Epi displays excellent robustness and generalization ability on both training datasets and independent datasets of K562 cell line. Further experiments confirm that iORI-Epi is highly scalable in other cell lines (MCF7 and HCT116). We also analyze and clarify the regulatory role of epigenomic marks, DNA motifs, and chromatin interaction in DNA replication initiation of eukaryotic genomes. Finally, we discuss gene enrichment pathways from the perspective of ORIs in different replication timing states and heuristically dissect the effect of promoters on replication initiation. Our computational methodology is worth extending to ORI identification in other eukaryotic species.

Abstract Image

Abstract Image

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融合表观基因组学和染色质相互作用信息的DNA复制起源准确鉴定。
DNA复制起始是一个复杂的过程,涉及各种遗传和表观基因组特征。正确识别复制起源(ORIs)可以为研究多种由复制引起的疾病提供重要线索。在此,我们设计了一种名为iORI-Epi的计算方法,通过结合基于表观基因组的特征、基于序列的特征和基于3D基因组的特征来识别ori。iORI-Epi对K562细胞系的训练数据集和独立数据集均表现出良好的鲁棒性和泛化能力。进一步的实验证实iORI-Epi在其他细胞系(MCF7和HCT116)中具有高度可扩展性。我们还分析和阐明了表观基因组标记、DNA基序和染色质相互作用在真核生物基因组DNA复制起始中的调控作用。最后,我们从不同复制时间状态的ORIs角度讨论了基因富集途径,并启发式剖析了启动子对复制起始的影响。我们的计算方法值得推广到其他真核生物物种的ORI鉴定。
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