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PEACOCK:一种机器学习方法,用于评估细胞类型特异性增强子-基因调控关系的有效性。

PEACOCK: a machine learning approach to assess the validity of cell type-specific enhancer-gene regulatory relationships.

机构信息

Division of Bioinformatics, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA.

Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA.

出版信息

NPJ Syst Biol Appl. 2023 Apr 3;9(1):9. doi: 10.1038/s41540-023-00270-z.

DOI:10.1038/s41540-023-00270-z
PMID:37012250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10070356/
Abstract

The vast majority of disease-associated variants identified in genome-wide association studies map to enhancers, powerful regulatory elements which orchestrate the recruitment of transcriptional complexes to their target genes' promoters to upregulate transcription in a cell type- and timing-dependent manner. These variants have implicated thousands of enhancers in many common genetic diseases, including nearly all cancers. However, the etiology of most of these diseases remains unknown because the regulatory target genes of the vast majority of enhancers are unknown. Thus, identifying the target genes of as many enhancers as possible is crucial for learning how enhancer regulatory activities function and contribute to disease. Based on experimental results curated from scientific publications coupled with machine learning methods, we developed a cell type-specific score predictive of an enhancer targeting a gene. We computed the score genome-wide for every possible cis enhancer-gene pair and validated its predictive ability in four widely used cell lines. Using a pooled final model trained across multiple cell types, all possible gene-enhancer regulatory links in cis (~17 M) were scored and added to the publicly available PEREGRINE database ( www.peregrineproj.org ). These scores provide a quantitative framework for the enhancer-gene regulatory prediction that can be incorporated into downstream statistical analyses.

摘要

在全基因组关联研究中发现的绝大多数与疾病相关的变异都映射到增强子上,增强子是一种强大的调控元件,能够协调转录复合物招募到其靶基因的启动子,以细胞类型和时间依赖的方式上调转录。这些变体已经涉及到许多常见遗传疾病中的数千个增强子,包括几乎所有的癌症。然而,由于绝大多数增强子的调控靶基因尚不清楚,这些疾病的大部分病因仍然未知。因此,尽可能多地识别增强子的靶基因对于了解增强子调控活动的功能以及它们如何导致疾病至关重要。基于从科学出版物中整理的实验结果以及机器学习方法,我们开发了一种细胞特异性评分方法,可预测增强子靶向基因。我们在全基因组范围内为每一个可能的顺式增强子-基因对计算了得分,并在四个广泛使用的细胞系中验证了其预测能力。使用跨多个细胞类型训练的 pooled 最终模型,对顺式(~17M)中所有可能的基因-增强子调控联系进行了评分,并将其添加到可公开获取的 PEREGRINE 数据库(www.peregrineproj.org)中。这些分数为增强子-基因调控预测提供了一个定量框架,可以整合到下游的统计分析中。

相似文献

1
PEACOCK: a machine learning approach to assess the validity of cell type-specific enhancer-gene regulatory relationships.PEACOCK:一种机器学习方法,用于评估细胞类型特异性增强子-基因调控关系的有效性。
NPJ Syst Biol Appl. 2023 Apr 3;9(1):9. doi: 10.1038/s41540-023-00270-z.
2
PEREGRINE: A genome-wide prediction of enhancer to gene relationships supported by experimental evidence.游隼:基于实验证据的全基因组预测增强子与基因关系。
PLoS One. 2020 Dec 15;15(12):e0243791. doi: 10.1371/journal.pone.0243791. eCollection 2020.
3
GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.基因增强子:基因卡片中增强子与靶基因的全基因组整合
Database (Oxford). 2017 Jan 1;2017. doi: 10.1093/database/bax028.
4
Bridging between Mouse and Human Enhancer-Promoter Long-Range Interactions in Neural Stem Cells, to Understand Enhancer Function in Neurodevelopmental Disease.在神经干细胞中连接小鼠和人类增强子-启动子长程相互作用,以理解神经发育性疾病中的增强子功能。
Int J Mol Sci. 2022 Jul 19;23(14):7964. doi: 10.3390/ijms23147964.
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Genome-wide maps of distal gene regulatory enhancers active in the human placenta.人类胎盘活跃的远端基因调控增强子的全基因组图谱。
PLoS One. 2018 Dec 27;13(12):e0209611. doi: 10.1371/journal.pone.0209611. eCollection 2018.
6
EnhancerDB: a resource of transcriptional regulation in the context of enhancers.EnhancerDB:增强子调控转录的资源数据库。
Database (Oxford). 2019 Jan 1;2019:bay141. doi: 10.1093/database/bay141.
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A curated benchmark of enhancer-gene interactions for evaluating enhancer-target gene prediction methods.一个经过精心策划的增强子-基因相互作用基准,用于评估增强子-靶基因预测方法。
Genome Biol. 2020 Jan 22;21(1):17. doi: 10.1186/s13059-019-1924-8.
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Genome-wide identification and characterization of DNA enhancers with a stacked multivariate fusion framework.基于堆叠多元融合框架的全基因组 DNA 增强子识别与特征分析。
PLoS Comput Biol. 2022 Dec 15;18(12):e1010779. doi: 10.1371/journal.pcbi.1010779. eCollection 2022 Dec.
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Genome-wide enhancer maps link risk variants to disease genes.全基因组增强子图谱将风险变异与疾病基因联系起来。
Nature. 2021 May;593(7858):238-243. doi: 10.1038/s41586-021-03446-x. Epub 2021 Apr 7.
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Opening up the blackbox: an interpretable deep neural network-based classifier for cell-type specific enhancer predictions.打开黑箱:一种基于可解释深度神经网络的细胞类型特异性增强子预测分类器。
BMC Syst Biol. 2016 Aug 1;10 Suppl 2(Suppl 2):54. doi: 10.1186/s12918-016-0302-3.

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Nat Rev Genet. 2025 Jun 30. doi: 10.1038/s41576-025-00862-x.
2
Cutting-edge AI tools revolutionizing scientific research in life sciences.前沿人工智能工具正在彻底改变生命科学领域的科学研究。
BioTechnologia (Pozn). 2025 Mar 31;106(1):77-102. doi: 10.5114/bta/200803. eCollection 2025.
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A deep learning model for DNA enhancer prediction based on nucleotide position aware feature encoding.一种基于核苷酸位置感知特征编码的DNA增强子预测深度学习模型。

本文引用的文献

1
Implications of Enhancer Transcription and eRNAs in Cancer.增强子转录和 eRNA 在癌症中的意义。
Cancer Res. 2021 Aug 15;81(16):4174-4182. doi: 10.1158/0008-5472.CAN-20-4010. Epub 2021 May 20.
2
Mechanisms of enhancer action: the known and the unknown.增强子作用的机制:已知的和未知的。
Genome Biol. 2021 Apr 15;22(1):108. doi: 10.1186/s13059-021-02322-1.
3
PEREGRINE: A genome-wide prediction of enhancer to gene relationships supported by experimental evidence.游隼:基于实验证据的全基因组预测增强子与基因关系。
iScience. 2024 May 19;27(6):110030. doi: 10.1016/j.isci.2024.110030. eCollection 2024 Jun 21.
PLoS One. 2020 Dec 15;15(12):e0243791. doi: 10.1371/journal.pone.0243791. eCollection 2020.
4
Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations.基于数千个 CRISPR 干扰的增强子-启动子调控的活性-接触模型。
Nat Genet. 2019 Dec;51(12):1664-1669. doi: 10.1038/s41588-019-0538-0. Epub 2019 Nov 29.
5
EnhancerAtlas 2.0: an updated resource with enhancer annotation in 586 tissue/cell types across nine species.EnhancerAtlas 2.0:一个更新的资源,包含了 9 个物种的 586 种组织/细胞类型中的增强子注释。
Nucleic Acids Res. 2020 Jan 8;48(D1):D58-D64. doi: 10.1093/nar/gkz980.
6
Long-range enhancer-promoter contacts in gene expression control.长程增强子-启动子相互作用在基因表达调控中的作用。
Nat Rev Genet. 2019 Aug;20(8):437-455. doi: 10.1038/s41576-019-0128-0.
7
SEdb: a comprehensive human super-enhancer database.SEdb:一个全面的人类超级增强子数据库。
Nucleic Acids Res. 2019 Jan 8;47(D1):D235-D243. doi: 10.1093/nar/gky1025.
8
HACER: an atlas of human active enhancers to interpret regulatory variants.HACER:人类活性增强子图谱,用于解读调控变体。
Nucleic Acids Res. 2019 Jan 8;47(D1):D106-D112. doi: 10.1093/nar/gky864.
9
Enhancer Activity Requires CBP/P300 Bromodomain-Dependent Histone H3K27 Acetylation.增强子活性需要 CBP/P300 溴结构域依赖性组蛋白 H3K27 乙酰化。
Cell Rep. 2018 Aug 14;24(7):1722-1729. doi: 10.1016/j.celrep.2018.07.041.
10
Enhancer redundancy provides phenotypic robustness in mammalian development.增强子冗余为哺乳动物发育提供表型稳健性。
Nature. 2018 Feb 8;554(7691):239-243. doi: 10.1038/nature25461. Epub 2018 Jan 31.