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线虫,一种非传统的衰老和阿尔茨海默病自然模型中的基因组测序变异 。 (注:原文中“the ”后面缺少具体内容,这里只能根据已有信息尽量完整翻译)

Genome Sequencing Variations in the , an Unconventional Natural Model of Aging and Alzheimer's Disease.

作者信息

Hurley Michael J, Urra Claudio, Garduno B Maximiliano, Bruno Agostino, Kimbell Allison, Wilkinson Brent, Marino-Buslje Cristina, Ezquer Marcelo, Ezquer Fernando, Aburto Pedro F, Poulin Elie, Vasquez Rodrigo A, Deacon Robert, Avila Ariel, Altimiras Francisco, Whitney Vanderklish Peter, Zampieri Guido, Angione Claudio, Constantino Gabriele, Holmes Todd C, Coba Marcelo P, Xu Xiangmin, Cogram Patricia

机构信息

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom.

Department of Ecological Sciences, Faculty of Sciences, Institute of Ecology and Biodiversity, Universidad de Chile, Santiago, Chile.

出版信息

Front Aging Neurosci. 2022 Jun 30;14:894994. doi: 10.3389/fnagi.2022.894994. eCollection 2022.

Abstract

The degu () is a diurnal long-lived rodent that can spontaneously develop molecular and behavioral changes that mirror those seen in human aging. With age some degu, but not all individuals, develop cognitive decline and brain pathology like that observed in Alzheimer's disease including neuroinflammation, hyperphosphorylated tau and amyloid plaques, together with other co-morbidities associated with aging such as macular degeneration, cataracts, alterations in circadian rhythm, diabetes and atherosclerosis. Here we report the whole-genome sequencing and analysis of the degu genome, which revealed unique features and molecular adaptations consistent with aging and Alzheimer's disease. We identified single nucleotide polymorphisms in genes associated with Alzheimer's disease including a novel apolipoprotein E () gene variant that correlated with an increase in amyloid plaques in brain and modified the predicted degu APOE protein structure and functionality. The reported genome of an unconventional long-lived animal model of aging and Alzheimer's disease offers the opportunity for understanding molecular pathways involved in aging and should help advance biomedical research into treatments for Alzheimer's disease.

摘要

八齿鼠()是一种昼行性的长寿啮齿动物,它会自发出现一些分子和行为变化,这些变化与人类衰老过程中出现的变化相似。随着年龄增长,部分八齿鼠(并非所有个体)会出现认知能力下降和脑部病变,类似于阿尔茨海默病中观察到的情况,包括神经炎症、tau蛋白过度磷酸化和淀粉样斑块,同时还伴有其他与衰老相关的合并症,如黄斑变性、白内障、昼夜节律改变、糖尿病和动脉粥样硬化。在此,我们报告了八齿鼠基因组的全基因组测序和分析结果,该结果揭示了与衰老和阿尔茨海默病一致的独特特征和分子适应性。我们在与阿尔茨海默病相关的基因中鉴定出单核苷酸多态性,包括一种新的载脂蛋白E()基因变体,该变体与大脑中淀粉样斑块的增加相关,并改变了预测的八齿鼠载脂蛋白E蛋白结构和功能。所报道的这种非常规的衰老和阿尔茨海默病长寿动物模型的基因组,为理解衰老过程中涉及的分子途径提供了机会,并应有助于推进针对阿尔茨海默病治疗的生物医学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e4d/9291219/e8804a152b82/fnagi-14-894994-g0001.jpg

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