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转录后基因调控中可变聚腺苷酸化和剪接的计算方法

Computational methods for alternative polyadenylation and splicing in post-transcriptional gene regulation.

作者信息

Fahmi Naima Ahmed, Saha Sourav, Song Qianqian, Lou Qian, Yong Jeongsik, Zhang Wei

机构信息

Department of Computer Science, University of Central Florida, Orlando, FL, USA.

Department of Health Outcomes and Biomedical Informatics, University of Florida, Gainesville, FL, USA.

出版信息

Exp Mol Med. 2025 Aug 14. doi: 10.1038/s12276-025-01496-z.

Abstract

Alternative polyadenylation (APA) and alternative splicing (AS) are essential post-transcriptional mechanisms that enhance transcriptome diversity and regulate gene expression across various biological contexts. APA modifies transcript stability, localization and translation efficiency by generating mRNA isoforms with distinct 3' untranslated regions or coding sequences, while AS alters protein diversity through exon inclusion or exclusion. The advent of high-throughput RNA sequencing has driven the development of computational methods to systematically identify, quantify and analyze APA and AS events, shedding light on their regulatory roles in normal physiology and disease. These methods can be broadly categorized based on their underlying methodologies and the data types they process, with specialized tools designed for both bulk and single-cell RNA sequencing. Here, in this Review, we provide a comprehensive overview of computational strategies for APA and AS detection and differential analysis, highlighting their advantages, limitations and applications. In addition, we explore techniques specifically tailored for single-cell RNA sequencing. We enhance our understanding of APA and AS regulation across diverse biological systems by summarizing recent advancements, offering new insights into gene regulation at both the population and single-cell levels.

摘要

可变聚腺苷酸化(APA)和可变剪接(AS)是重要的转录后机制,可增强转录组多样性并在各种生物学背景下调节基因表达。APA通过产生具有不同3'非翻译区或编码序列的mRNA异构体来改变转录本稳定性、定位和翻译效率,而AS则通过外显子包含或排除来改变蛋白质多样性。高通量RNA测序的出现推动了计算方法的发展,以系统地识别、量化和分析APA和AS事件,揭示它们在正常生理学和疾病中的调控作用。这些方法可根据其基础方法和处理的数据类型大致分类,有专门为批量和单细胞RNA测序设计的工具。在此综述中,我们全面概述了用于APA和AS检测及差异分析的计算策略,突出它们的优点、局限性和应用。此外,我们探索了专门为单细胞RNA测序量身定制的技术。通过总结近期进展,我们加深了对不同生物系统中APA和AS调控的理解,为群体和单细胞水平的基因调控提供了新见解。

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