Chronic RNA G-quadruplex Accumulation in Aging and Alzheimer's Disease.

Lena Kallweit, Eric D Hamlett, Hannah Saternos, Anah Gilmore, Ann-Charlotte Granholm, Scott Horowitz
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Abstract

Introduction: As the world population ages, new molecular targets in aging and Alzheimer's Disease (AD) are needed to combat the expected influx of new AD cases. Until now, the role of RNA structure in aging and neurodegeneration has largely remained unexplored. METHODS: In this study, we examined human hippocampal postmortem tissue for the formation of RNA G-quadruplexes (rG4s) in aging and AD.

Results: We found that rG4 immunostaining strongly increased in the hippocampus with both age and with AD severity. We further found that neurons with accumulation of phospho-tau immunostaining contained rG4s, that rG4 structure can drive tau aggregation, and that rG4 staining density depended on APOE genotype in the human tissue examined.

Discussion: Combined with previous studies showing the dependence of rG4 structure on stress and the extreme power of rG4s at oligomerizing proteins, we propose a model of neurodegeneration in which chronic rG4 formation is linked to proteostasis collapse. These morphological findings suggest that further investigation of RNA structure in neurodegeneration is a critical avenue for future treatments and diagnoses.

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RNA G-四链体在衰老和阿尔茨海默病中的新作用。
随着世界人口的老龄化,需要针对老龄化和阿尔茨海默病(AD)的新分子靶点来对抗预期涌入的新AD病例。到目前为止,RNA结构在衰老和神经退行性变中的作用在很大程度上尚未被探索。在这项研究中,我们检查了衰老和AD患者海马死后组织中RNA G-四链体(rG4s)的形成。我们发现,随着年龄和AD严重程度的增加,rG4免疫染色在海马中的患病率显著增加。我们进一步发现,神经原纤维缠结(NFT)含有rG4s,rG4结构可以驱动tau聚集,并且rG4的形成取决于所检查的人类组织中的APOE基因型。结合先前显示rG4结构对应激的依赖性以及rG4在寡聚蛋白方面的极端能力的研究,我们提出了一种神经退行性变模型,其中慢性rG4的形成驱动蛋白稳定崩溃。我们提出,进一步研究神经退行性变中的RNA结构是未来治疗和诊断的关键途径。
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