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snRNA-seq 分析多核肌源性 FSHD 细胞,鉴定与胚胎样程序激活和氧化应激诱导细胞凋亡相关的异质性 FSHD 转录组特征。

snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis.

机构信息

Department of Human Genetics, Leiden University Medical Center, Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.

Division of Human Biology, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, Seattle, WA 98109, USA.

出版信息

Hum Mol Genet. 2024 Jan 20;33(3):284-298. doi: 10.1093/hmg/ddad186.

Abstract

The sporadic nature of DUX4 expression in FSHD muscle challenges comparative transcriptome analyses between FSHD and control samples. A variety of DUX4 and FSHD-associated transcriptional changes have been identified, but bulk RNA-seq strategies prohibit comprehensive analysis of their spatiotemporal relation, interdependence and role in the disease process. In this study, we used single-nucleus RNA-sequencing of nuclei isolated from patient- and control-derived multinucleated primary myotubes to investigate the cellular heterogeneity in FSHD. Taking advantage of the increased resolution in snRNA-sequencing of fully differentiated myotubes, two distinct populations of DUX4-affected nuclei could be defined by their transcriptional profiles. Our data provides insights into the differences between these two populations and suggests heterogeneity in two well-known FSHD-associated transcriptional aberrations: increased oxidative stress and inhibition of myogenic differentiation. Additionally, we provide evidence that DUX4-affected nuclei share transcriptome features with early embryonic cells beyond the well-described cleavage stage, progressing into the 8-cell and blastocyst stages. Altogether, our data suggests that the FSHD transcriptional profile is defined by a mixture of individual and sometimes mutually exclusive DUX4-induced responses and cellular state-dependent downstream effects.

摘要

DUX4 表达在 FSHD 肌肉中的散发性挑战了 FSHD 和对照样本之间的比较转录组分析。已经确定了各种 DUX4 和 FSHD 相关的转录变化,但批量 RNA-seq 策略禁止对其时空关系、相互依存性及其在疾病过程中的作用进行全面分析。在这项研究中,我们使用从患者和对照衍生的多核原代肌管中分离的细胞核进行单细胞 RNA-seq,以研究 FSHD 中的细胞异质性。利用完全分化的肌管中 snRNA-seq 的分辨率提高,我们可以根据其转录谱定义两种不同的 DUX4 影响的核群体。我们的数据提供了对这两个群体之间差异的深入了解,并表明在两种众所周知的 FSHD 相关转录异常中存在异质性:氧化应激增加和肌生成分化抑制。此外,我们提供的证据表明,受 DUX4 影响的核与早期胚胎细胞共享转录组特征,超出了描述明确的卵裂阶段,进入 8 细胞和囊胚阶段。总之,我们的数据表明,FSHD 的转录谱是由个体和有时相互排斥的 DUX4 诱导反应以及细胞状态依赖性下游效应的混合物定义的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43c0/10800016/1567d4357cfd/ddad186f1.jpg

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