衰老与帕金森病体细胞突变的RNA序列分析。

Shixiang Sun, Daisy Sproviero, César Payán-Gómez, Jan H J Hoeijmakers, Alexander Y Maslov, Pier G Mastroberardino, Jan Vijg
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摘要

帕金森病(PD)是一种与年龄相关的神经退行性疾病,与DNA损伤增加有关。为了测试PD是否与体细胞突变增加有关,我们分析了5次帕金森进展标记计划中克隆扩增体细胞变异的全血RNA-seq数据。对rna测序数据的综合分析显示,共有5927个体细胞变异(平均每个样本2.4个变异)。与上次访问时的对照组相比,PD受试者的突变频率显着升高。黑质RNA分析证实了这一点。相比之下,老年PD患者中克隆造血的携带者比例与老年健康对照相比显著降低。这些结果表明,虽然PD的总体突变率较高,但特异性克隆扩增突变对PD具有保护作用,正如在阿尔茨海默病中发现的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA sequence analysis of somatic mutations in aging and Parkinson's Disease.

Parkinson's Disease (PD) is an age-related neurodegenerative disorder that has been associated with increased DNA damage. To test if PD is associated with increased somatic mutations, we analyzed RNA-seq data in whole blood from 5 visits of the Parkinson's Progression Markers Initiative for clonally amplified somatic variants. Comprehensive analysis of RNA-sequencing data revealed a total of 5,927 somatic variants (2.4 variants per sample on average). Mutation frequencies were significantly elevated in PD subjects as compared to agematched controls at the time of the last visit. This was confirmed by RNA analysis of substantia nigra. By contrast, the fraction of carriers with clonal hematopoiesis, was significantly reduced in old PD patients as compared to old healthy controls. These results indicate that while the overall mutation rate is higher in PD, specific clonally amplified mutations are protective against PD, as has been found for Alzheimer's Disease.

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