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单细胞数据中的微小RNA调控与基因表达变异性分析

Analysis of MicroRNA Regulation and Gene Expression Variability in Single Cell Data.

作者信息

Liu Wendao, Shomron Noam

机构信息

Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

Edmond J. Safra Center for Bioinformatics, Tel Aviv University, Tel Aviv 6329302, Israel.

出版信息

J Pers Med. 2022 Oct 21;12(10):1750. doi: 10.3390/jpm12101750.

DOI:10.3390/jpm12101750
PMID:36294889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9605646/
Abstract

MicroRNAs (miRNAs) regulate gene expression by binding to mRNAs, and thus reduce target gene expression levels and expression variability, also known as 'noise'. Single-cell RNA sequencing (scRNA-seq) technology has been used to study miRNA and mRNA expression in single cells. To evaluate scRNA-seq as a tool for investigating miRNA regulation, we analyzed datasets with both mRNA and miRNA expression in single-cell format. We found that miRNAs slightly reduce the expression noise of target genes; however, this effect is easily masked by strong technical noise from scRNA-seq. We suggest improvements aimed at reducing technical noise, which can be implemented in experimental design and computational analysis prior to running scRNA-seq. Our study provides useful guidelines for experiments that evaluate the effect of miRNAs on mRNA expression from scRNA-seq.

摘要

微小RNA(miRNA)通过与信使核糖核酸(mRNA)结合来调控基因表达,从而降低靶基因的表达水平和表达变异性,即所谓的“噪音”。单细胞RNA测序(scRNA-seq)技术已被用于研究单细胞中的miRNA和mRNA表达。为了评估scRNA-seq作为研究miRNA调控工具的有效性,我们分析了单细胞形式的mRNA和miRNA表达数据集。我们发现,miRNA会略微降低靶基因的表达噪音;然而,这种效应很容易被scRNA-seq产生的强烈技术噪音所掩盖。我们建议进行改进以减少技术噪音,这些改进可以在进行scRNA-seq之前的实验设计和计算分析中实施。我们的研究为评估miRNA对scRNA-seq中mRNA表达影响的实验提供了有用的指导方针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f5/9605646/52a13cc906f4/jpm-12-01750-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f5/9605646/707528b0f015/jpm-12-01750-g0A3.jpg
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本文引用的文献

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BMC Bioinformatics. 2022 Jul 22;23(1):291. doi: 10.1186/s12859-022-04814-8.
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miRDB: an online database for prediction of functional microRNA targets.miRDB:一个用于预测功能 microRNA 靶标的在线数据库。
Nucleic Acids Res. 2020 Jan 8;48(D1):D127-D131. doi: 10.1093/nar/gkz757.
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Single-cell RNA-seq denoising using a deep count autoencoder.
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Characterizing noise structure in single-cell RNA-seq distinguishes genuine from technical stochastic allelic expression.表征单细胞RNA测序中的噪声结构可区分真实的与技术上的随机等位基因表达。
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