IVEA:预测增强子-基因调控相互作用的综合变异贝叶斯推理方法。

IF 2.4 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Bioinformatics advances Pub Date : 2024-08-20 eCollection Date: 2024-01-01 DOI:10.1093/bioadv/vbae118
Yasumasa Kimura, Yoshimasa Ono, Kotoe Katayama, Seiya Imoto
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引用次数: 0

摘要

动机增强子在细胞类型特异性转录调控中发挥着关键作用。尽管已鉴定出数千个候选增强子,但揭示它们与其靶基因之间的调控关系仍具有挑战性。因此,需要用计算方法来准确推断增强子与基因的调控关系:在这项研究中,我们提出了一种新方法 IVEA,它可以通过估计启动子和增强子的活性来预测增强子与基因之间的调控相互作用。其统计模型基于转录突变的基因调控机制,该机制的特点是突变大小和频率分别由启动子和增强子控制。利用转录读数、染色质可及性和染色质接触数据作为输入,使用变异贝叶斯推理估算启动子和增强子的活性,并计算出每对增强子-启动子对目标基因转录的贡献。我们的分析表明,所提出的方法可以达到很高的预测精度,并提供与生物学相关的增强子-基因调控相互作用:IVEA 代码可在 GitHub 上获取:https://github.com/yasumasak/ivea。本研究中使用的公开数据集见补充表 S4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IVEA: an integrative variational Bayesian inference method for predicting enhancer-gene regulatory interactions.

Motivation: Enhancers play critical roles in cell-type-specific transcriptional control. Despite the identification of thousands of candidate enhancers, unravelling their regulatory relationships with their target genes remains challenging. Therefore, computational approaches are needed to accurately infer enhancer-gene regulatory relationships.

Results: In this study, we propose a new method, IVEA, that predicts enhancer-gene regulatory interactions by estimating promoter and enhancer activities. Its statistical model is based on the gene regulatory mechanism of transcriptional bursting, which is characterized by burst size and frequency controlled by promoters and enhancers, respectively. Using transcriptional readouts, chromatin accessibility, and chromatin contact data as inputs, promoter and enhancer activities were estimated using variational Bayesian inference, and the contribution of each enhancer-promoter pair to target gene transcription was calculated. Our analysis demonstrates that the proposed method can achieve high prediction accuracy and provide biologically relevant enhancer-gene regulatory interactions.

Availability and implementation: The IVEA code is available on GitHub at https://github.com/yasumasak/ivea. The publicly available datasets used in this study are described in Supplementary Table S4.

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