生物
祖细胞
干细胞
造血
基因亚型
选择性拼接
细胞生物学
基因表达谱
RNA剪接
基因表达
电池类型
计算生物学
基因
细胞
遗传学
核糖核酸
作者
Laura Mincarelli,Vladimir Uzun,David J. Wright,Anita Scoones,Stuart A. Rushworth,Wilfried Haerty,Iain C. Macaulay
标识
DOI:10.1038/s42003-023-04936-6
摘要
Abstract Single-cell approaches have revealed that the haematopoietic hierarchy is a continuum of differentiation, from stem cell to committed progenitor, marked by changes in gene expression. However, many of these approaches neglect isoform-level information and thus do not capture the extent of alternative splicing within the system. Here, we present an integrated short- and long-read single-cell RNA-seq analysis of haematopoietic stem and progenitor cells. We demonstrate that over half of genes detected in standard short-read single-cell analyses are expressed as multiple, often functionally distinct, isoforms, including many transcription factors and key cytokine receptors. We observe global and HSC-specific changes in gene expression with ageing but limited impact of ageing on isoform usage. Integrating single-cell and cell-type-specific isoform landscape in haematopoiesis thus provides a new reference for comprehensive molecular profiling of heterogeneous tissues, as well as novel insights into transcriptional complexity, cell-type-specific splicing events and consequences of ageing.
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