帕金森病的单核多组学揭示了谷氨酸能神经元亚型容易通过改变转录网络而导致基因失调。

IF 6.2 2区 医学 Q1 NEUROSCIENCES Acta Neuropathologica Communications Pub Date : 2024-07-02 DOI:10.1186/s40478-024-01803-1
E Keats Shwab, Daniel C Gingerich, Zhaohui Man, Julia Gamache, Melanie E Garrett, Gregory E Crawford, Allison E Ashley-Koch, Geidy E Serrano, Thomas G Beach, Michael W Lutz, Ornit Chiba-Falek
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引用次数: 0

摘要

帕金森病(PD)的基因结构复杂,多种脑细胞亚型参与了该病的神经病理学进展。在这里,我们的目标是在细胞亚型精确水平上推进我们对帕金森病遗传复杂性的理解。利用并行的单核(sn)RNA-seq 和 snATAC-seq 分析,我们以颗粒状单细胞分辨率同时分析了 12 名帕金森病患者和 12 名对照组患者颞叶皮层组织的转录组和染色质可及性景观。为分析这些 snMulti-omics 数据集,我们开发并应用了一个综合生物信息学管道。研究结果发现了一个皮质谷氨酸能兴奋神经元亚群,该亚群在帕金森病中的基因表达发生了显著变化,其中包括在全基因组关联研究(GWAS)中发现的帕金森病风险位点内的差异表达基因。这是唯一一种显示出 SNCA 显著、稳健过表达的神经元亚型。对这一神经元亚群的进一步表征显示,与轴突导向、神经元生长和突触后结构相关的特定通路上调,而与突触前组织和钙反应相关的通路下调。此外,我们还研究了三种分子机制在调控PD相关细胞亚型特异性基因表达失调中的作用:(1)顺式调控元件对转录机制的可及性变化;(2)主转录调控因子(包括YY1、SP3和KLF16)丰度的变化;(3)与影响转录因子结合亲和力的PD-GWAS基因组变异高度连锁不平衡的候选调控变异。据我们所知,这项研究是首次在细胞亚型分辨率上对帕金森病的多组学图谱进行最全面的研究。我们的研究结果提供了关于谷氨酸能神经元细胞亚型、致病基因和非编码调控变异的新见解,这些变异是导致帕金森病神经病理学进展的基础,为开发细胞和基因靶向治疗药物以阻止疾病进展以及用于早期临床前诊断的基因生物标记物铺平了道路。
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Single-nucleus multi-omics of Parkinson's disease reveals a glutamatergic neuronal subtype susceptible to gene dysregulation via alteration of transcriptional networks.

The genetic architecture of Parkinson's disease (PD) is complex and multiple brain cell subtypes are involved in the neuropathological progression of the disease. Here we aimed to advance our understanding of PD genetic complexity at a cell subtype precision level. Using parallel single-nucleus (sn)RNA-seq and snATAC-seq analyses we simultaneously profiled the transcriptomic and chromatin accessibility landscapes in temporal cortex tissues from 12 PD compared to 12 control subjects at a granular single cell resolution. An integrative bioinformatic pipeline was developed and applied for the analyses of these snMulti-omics datasets. The results identified a subpopulation of cortical glutamatergic excitatory neurons with remarkably altered gene expression in PD, including differentially-expressed genes within PD risk loci identified in genome-wide association studies (GWAS). This was the only neuronal subtype showing significant and robust overexpression of SNCA. Further characterization of this neuronal-subpopulation showed upregulation of specific pathways related to axon guidance, neurite outgrowth and post-synaptic structure, and downregulated pathways involved in presynaptic organization and calcium response. Additionally, we characterized the roles of three molecular mechanisms in governing PD-associated cell subtype-specific dysregulation of gene expression: (1) changes in cis-regulatory element accessibility to transcriptional machinery; (2) changes in the abundance of master transcriptional regulators, including YY1, SP3, and KLF16; (3) candidate regulatory variants in high linkage disequilibrium with PD-GWAS genomic variants impacting transcription factor binding affinities. To our knowledge, this study is the first and the most comprehensive interrogation of the multi-omics landscape of PD at a cell-subtype resolution. Our findings provide new insights into a precise glutamatergic neuronal cell subtype, causal genes, and non-coding regulatory variants underlying the neuropathological progression of PD, paving the way for the development of cell- and gene-targeted therapeutics to halt disease progression as well as genetic biomarkers for early preclinical diagnosis.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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