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环状 RNA 编码的淀粉样 β 肽——阿尔茨海默病的一个新的潜在参与者。

Circular RNA Encoded Amyloid Beta peptides-A Novel Putative Player in Alzheimer's Disease.

机构信息

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9b, 50931 Cologne, Germany.

VIB-KU Leuven Center for Brain & Disease Research, KU Leuven, O&N IV Herestraat 49-box 602, 3000 Leuven, Belgium.

出版信息

Cells. 2020 Sep 29;9(10):2196. doi: 10.3390/cells9102196.

Abstract

Alzheimer's disease (AD) is an age-related detrimental dementia. Amyloid beta peptides (Aβ) play a crucial role in the pathology of AD. In familial AD, Aβ are generated from the full-length amyloid beta precursor protein (APP) via dysregulated proteolytic processing; however, in the case of sporadic AD, the mechanism of Aβ biogenesis remains elusive. circRNAs are a class of transcripts preferentially expressed in brain. We identified a circRNA harboring the Aβ-coding region of the gene termed circAβ-a. This circular RNA was detected in the brains of AD patients and non-dementia controls. With the aid of our recently established approach for analysis of circRNA functions, we demonstrated that circAβ-a is efficiently translated into a novel Aβ-containing Aβ175 polypeptide (19.2 KDa) in both cultured cells and human brain. Furthermore, Aβ175 was shown to be processed into Aβ peptides-a hallmark of AD. In summary, our analysis revealed an alternative pathway of Aβ biogenesis. Consequently, circAβ-a and its corresponding translation product could potentially represent novel therapeutic targets for AD treatment. Importantly, our data point to yet another evolutionary route for potentially increasing proteome complexity by generating additional polypeptide variants using back-splicing of primary transcripts that yield circular RNA templates.

摘要

阿尔茨海默病(AD)是一种与年龄相关的进行性痴呆。β淀粉样肽(Aβ)在 AD 的病理学中起着至关重要的作用。在家族性 AD 中,Aβ通过失调的蛋白水解加工从全长淀粉样前体蛋白(APP)产生;然而,在散发性 AD 的情况下,Aβ生物发生的机制仍不清楚。circRNAs 是一类在大脑中优先表达的转录本。我们鉴定了一种含有 APP 基因的 Aβ 编码区的 circRNA,称为 circAβ-a。这种环状 RNA 存在于 AD 患者和非痴呆对照者的大脑中。借助我们最近建立的分析 circRNA 功能的方法,我们证明 circAβ-a 可在培养细胞和人脑内有效地翻译为一种新型的含有 Aβ 的 Aβ175 多肽(19.2 kDa)。此外,还证明 Aβ175 被加工成 Aβ 肽,这是 AD 的一个标志。总之,我们的分析揭示了 Aβ 生物发生的另一种途径。因此,circAβ-a 及其相应的翻译产物可能代表 AD 治疗的新的治疗靶点。重要的是,我们的数据表明,通过使用产生环状 RNA 模板的初级转录物的反向剪接产生额外的多肽变体,可以为增加蛋白质组复杂性提供另一种进化途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/679c/7650678/34626fd2c907/cells-09-02196-g001.jpg

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