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转录组分析揭示了 tau 同工型驱动的转座子和基因表达变化。

Transcriptome analyses reveal tau isoform-driven changes in transposable element and gene expression.

机构信息

Department of Neurosciences, University of California, San Diego, La Jolla, CA, United States of America.

Veterans Affairs San Diego Healthcare System, San Diego, CA, United States of America.

出版信息

PLoS One. 2021 Sep 29;16(9):e0251611. doi: 10.1371/journal.pone.0251611. eCollection 2021.

Abstract

Alternative splicing of the gene MAPT produces several isoforms of tau protein. Overexpression of these isoforms is characteristic of tauopathies, which are currently untreatable neurodegenerative diseases. Though non-canonical functions of tau have drawn interest, the role of tau isoforms in these diseases has not been fully examined and may reveal new details of tau-driven pathology. In particular, tau has been shown to promote activation of transposable elements-highly regulated nucleotide sequences that replicate throughout the genome and can promote immunologic responses and cellular stress. This study examined tau isoforms' roles in promoting cell damage and dysregulation of genes and transposable elements at a family-specific and locus-specific level. We performed immunofluorescence, Western blot and cytotoxicity assays, along with paired-end RNA sequencing on differentiated SH-SY5Y cells infected with lentiviral constructs of tau isoforms and treated with amyloid-beta oligomers. Our transcriptomic findings were validated using publicly available RNA-sequencing data from Alzheimer's disease, progressive supranuclear palsy and control human samples from the Accelerating Medicine's Partnership for AD (AMP-AD). Significance for biochemical assays was determined using Wilcoxon ranked-sum tests and false discovery rate. Transcriptome analysis was conducted through DESeq2 and the TEToolkit suite available from the Hammell lab at Cold Spring Harbor Laboratory. Our analyses show overexpression of different tau isoforms and their interactions with amyloid-beta in SH-SY5Y cells result in isoform-specific changes in the transcriptome, with locus-specific transposable element dysregulation patterns paralleling those seen in patients with Alzheimer's disease and progressive supranuclear palsy. Locus-level transposable element expression showed increased dysregulation of L1 and Alu sites, which have been shown to drive pathology in other neurological diseases. We also demonstrated differences in rates of cell death in SH-SY5Y cells depending on tau isoform overexpression. These results demonstrate the importance of examining tau isoforms' role in neurodegeneration and of further examining transposable element dysregulation in tauopathies and its role in activating the innate immune system.

摘要

基因 MAPT 的可变剪接产生几种 tau 蛋白异构体。这些异构体的过表达是 tau 病的特征,目前尚无治疗方法的神经退行性疾病。虽然 tau 的非典型功能引起了关注,但 tau 异构体在这些疾病中的作用尚未得到充分研究,可能揭示 tau 驱动的病理学的新细节。特别是,tau 已被证明可以促进转座元件的激活——高度调控的核苷酸序列,这些序列可以在整个基因组中复制,并可以促进免疫反应和细胞应激。这项研究检查了 tau 异构体在促进细胞损伤和基因和转座元件的失调方面的作用,这是一种家族特异性和基因座特异性的水平。我们对感染了 tau 异构体慢病毒构建体并用淀粉样蛋白-β寡聚体处理的分化 SH-SY5Y 细胞进行了免疫荧光、western blot 和细胞毒性测定,以及配对末端 RNA 测序。我们使用来自阿尔茨海默病、进行性核上性麻痹和加速医学伙伴关系 AD (AMP-AD)的对照人类样本的公共可用 RNA-seq 数据验证了我们的转录组学发现。使用 Wilcoxon 秩和检验和错误发现率确定生物化学测定的显著性。转录组分析通过 DESeq2 和来自冷泉港实验室 Hammell 实验室的 TEToolkit 套件进行。我们的分析表明,不同 tau 异构体的过表达及其与淀粉样蛋白-β的相互作用导致 SH-SY5Y 细胞中转录组的异构体特异性变化,基因座特异性转座元件失调模式与阿尔茨海默病和进行性核上性麻痹患者相似。基因座水平的转座元件表达显示 L1 和 Alu 位点的失调增加,这些位点已被证明在其他神经退行性疾病中导致病理学。我们还证明了 SH-SY5Y 细胞中依赖于 tau 异构体过表达的细胞死亡率的差异。这些结果表明,检查 tau 异构体在神经退行性变中的作用以及进一步检查 tau 病中转座元件失调及其在激活固有免疫系统中的作用的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c7/8480850/96a9db7663ef/pone.0251611.g001.jpg

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