Suppr超能文献

量化转录组多样性:综述。

Quantifying transcriptome diversity: a review.

机构信息

The Department of Cell, Developmental and Integrative Biology, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Brief Funct Genomics. 2024 Mar 20;23(2):83-94. doi: 10.1093/bfgp/elad019.

Abstract

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.

摘要

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。

相似文献

1
Quantifying transcriptome diversity: a review.
Brief Funct Genomics. 2024 Mar 20;23(2):83-94. doi: 10.1093/bfgp/elad019.
4
Bayesian nonparametric discovery of isoforms and individual specific quantification.
Nat Commun. 2018 Apr 27;9(1):1681. doi: 10.1038/s41467-018-03402-w.
5
The Lived Experience of Autistic Adults in Employment: A Systematic Search and Synthesis.
Autism Adulthood. 2024 Dec 2;6(4):495-509. doi: 10.1089/aut.2022.0114. eCollection 2024 Dec.
6
Comprehensive mutational profiling identifies new driver events in cutaneous leiomyosarcoma.
Br J Dermatol. 2025 Jan 24;192(2):335-343. doi: 10.1093/bjd/ljae386.
7
New insights for precision treatment of glioblastoma from analysis of single-cell lncRNA expression.
J Cancer Res Clin Oncol. 2021 Jul;147(7):1881-1895. doi: 10.1007/s00432-021-03584-9. Epub 2021 Mar 11.
8
Perplexity as a Metric for Isoform Diversity in the Human Transcriptome.
bioRxiv. 2025 Jul 2:2025.07.02.662769. doi: 10.1101/2025.07.02.662769.

引用本文的文献

1
Early developmental origins of cortical disorders modeled in human neural stem cells.
Nat Commun. 2025 Jul 9;16(1):6347. doi: 10.1038/s41467-025-61316-w.
2
Perplexity as a Metric for Isoform Diversity in the Human Transcriptome.
bioRxiv. 2025 Jul 2:2025.07.02.662769. doi: 10.1101/2025.07.02.662769.
5
Two detoxification enzyme genes, and , mediate the susceptibility to afidopyropen in .
Front Physiol. 2024 Dec 6;15:1478869. doi: 10.3389/fphys.2024.1478869. eCollection 2024.
8
CoSIA: an R Bioconductor package for CrOss Species Investigation and Analysis.
Bioinformatics. 2023 Dec 1;39(12). doi: 10.1093/bioinformatics/btad759.
9
Human transcriptional signature of protection after immunization and infectious challenge mosquito bites.
Hum Vaccin Immunother. 2023 Dec 15;19(3):2282693. doi: 10.1080/21645515.2023.2282693. Epub 2023 Nov 27.

本文引用的文献

1
Characterizing the landscape of gene expression variance in humans.
PLoS Genet. 2023 Jul 6;19(7):e1010833. doi: 10.1371/journal.pgen.1010833. eCollection 2023 Jul.
2
Context-aware transcript quantification from long-read RNA-seq data with Bambu.
Nat Methods. 2023 Aug;20(8):1187-1195. doi: 10.1038/s41592-023-01908-w. Epub 2023 Jun 12.
4
: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications.
F1000Res. 2021 May 11;10:374. doi: 10.12688/f1000research.51749.2. eCollection 2021.
5
Alternative splicing as a source of phenotypic diversity.
Nat Rev Genet. 2022 Nov;23(11):697-710. doi: 10.1038/s41576-022-00514-4. Epub 2022 Jul 12.
6
The Tsallis generalized entropy enhances the interpretation of transcriptomics datasets.
PLoS One. 2022 Apr 21;17(4):e0266618. doi: 10.1371/journal.pone.0266618. eCollection 2022.
7
acorde unravels functionally interpretable networks of isoform co-usage from single cell data.
Nat Commun. 2022 Apr 5;13(1):1828. doi: 10.1038/s41467-022-29497-w.
8
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue.
Nat Biotechnol. 2022 Jul;40(7):1082-1092. doi: 10.1038/s41587-022-01231-3. Epub 2022 Mar 7.
9
The SpliZ generalizes 'percent spliced in' to reveal regulated splicing at single-cell resolution.
Nat Methods. 2022 Mar;19(3):307-310. doi: 10.1038/s41592-022-01400-x. Epub 2022 Mar 3.
10
Statistics or biology: the zero-inflation controversy about scRNA-seq data.
Genome Biol. 2022 Jan 21;23(1):31. doi: 10.1186/s13059-022-02601-5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验