Predicting cell population-specific gene expression from genomic sequence.

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in bioinformatics Pub Date : 2024-03-04 eCollection Date: 2024-01-01 DOI:10.3389/fbinf.2024.1347276
Lieke Michielsen, Marcel J T Reinders, Ahmed Mahfouz
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引用次数: 0

Abstract

Most regulatory elements, especially enhancer sequences, are cell population-specific. One could even argue that a distinct set of regulatory elements is what defines a cell population. However, discovering which non-coding regions of the DNA are essential in which context, and as a result, which genes are expressed, is a difficult task. Some computational models tackle this problem by predicting gene expression directly from the genomic sequence. These models are currently limited to predicting bulk measurements and mainly make tissue-specific predictions. Here, we present a model that leverages single-cell RNA-sequencing data to predict gene expression. We show that cell population-specific models outperform tissue-specific models, especially when the expression profile of a cell population and the corresponding tissue are dissimilar. Further, we show that our model can prioritize GWAS variants and learn motifs of transcription factor binding sites. We envision that our model can be useful for delineating cell population-specific regulatory elements.

从基因组序列预测细胞群特异性基因表达。
大多数调控元件,尤其是增强子序列,都具有细胞群体特异性。甚至可以说,一组独特的调控元件就是细胞群体的定义。然而,要发现 DNA 中哪些非编码区域在何种情况下必不可少,从而发现哪些基因会表达,是一项艰巨的任务。一些计算模型通过直接从基因组序列预测基因表达来解决这一问题。这些模型目前仅限于预测批量测量,主要是针对特定组织进行预测。在这里,我们提出了一种利用单细胞 RNA 序列数据预测基因表达的模型。我们的研究表明,细胞群特异性模型优于组织特异性模型,尤其是当细胞群和相应组织的表达谱不同时。此外,我们的研究还表明,我们的模型可以确定 GWAS 变异的优先次序,并学习转录因子结合位点的图案。我们设想,我们的模型可用于划分细胞群特异性调控元件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.60
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0.00%
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