The Department of Cell, Developmental and Integrative Biology, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, AL, USA.
Brief Funct Genomics. 2024 Mar 20;23(2):83-94. doi: 10.1093/bfgp/elad019.
Following the central dogma of molecular biology, gene expression heterogeneity can aid in predicting and explaining the wide variety of protein products, functions and, ultimately, heterogeneity in phenotypes. There is currently overlapping terminology used to describe the types of diversity in gene expression profiles, and overlooking these nuances can misrepresent important biological information. Here, we describe transcriptome diversity as a measure of the heterogeneity in (1) the expression of all genes within a sample or a single gene across samples in a population (gene-level diversity) or (2) the isoform-specific expression of a given gene (isoform-level diversity). We first overview modulators and quantification of transcriptome diversity at the gene level. Then, we discuss the role alternative splicing plays in driving transcript isoform-level diversity and how it can be quantified. Additionally, we overview computational resources for calculating gene-level and isoform-level diversity for high-throughput sequencing data. Finally, we discuss future applications of transcriptome diversity. This review provides a comprehensive overview of how gene expression diversity arises, and how measuring it determines a more complete picture of heterogeneity across proteins, cells, tissues, organisms and species.
按照分子生物学的中心法则,基因表达的异质性有助于预测和解释蛋白质产物、功能的广泛多样性,最终有助于解释表型的异质性。目前,用于描述基因表达谱多样性类型的术语存在重叠,忽视这些细微差别可能会错误地表示重要的生物学信息。在这里,我们将转录组多样性描述为衡量(1)样本中所有基因表达或群体中单个基因在样本间表达的异质性(基因水平的多样性)或(2)特定基因的异构体特异性表达的一种手段(异构体水平的多样性)。我们首先概述了基因水平转录组多样性的调节剂和定量方法。然后,我们讨论了可变剪接在驱动转录本异构体水平多样性方面的作用,以及如何对其进行量化。此外,我们还概述了用于计算高通量测序数据基因水平和异构体水平多样性的计算资源。最后,我们讨论了转录组多样性的未来应用。本综述全面概述了基因表达多样性的产生方式,以及如何衡量它可以更全面地了解蛋白质、细胞、组织、生物体和物种之间的异质性。