Chronic RNA G-quadruplex accumulation in aging and Alzheimer's disease.

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-02-24 DOI:10.7554/eLife.105446
Lena Kallweit, Eric Daniel Hamlett, Hannah Saternos, Anah Gilmore, Ann-Charlotte Granholm, Scott Horowitz
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Abstract

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. In this study, we examined human hippocampal postmortem tissue for the formation of RNA G-quadruplexes (rG4s) in aging and AD. We found that rG4 immunostaining strongly increased in the hippocampus with both age and with AD severity. We further found that neurons with the accumulation of phospho-tau immunostaining contained rG4s, rG4 structure can drive tau aggregation, and rG4 staining density depended on APOE genotype in the human tissue examined. 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.

随着世界人口老龄化的加剧,我们需要在衰老和阿尔茨海默病(AD)方面找到新的分子靶点,以应对预计将涌现的新的阿尔茨海默病病例。迄今为止,RNA结构在衰老和神经退行性变中的作用在很大程度上仍未得到探索。在这项研究中,我们研究了人类海马死后组织在衰老和注意力缺失症中 RNA G-四倍体(rG4s)的形成。我们发现,海马中的rG4免疫染色随着年龄和AD严重程度的增加而强烈增加。我们进一步发现,磷酸化tau免疫染色积累的神经元含有rG4s,rG4结构可驱动tau聚集,而且在所研究的人体组织中,rG4染色密度取决于APOE基因型。结合之前的研究,我们提出了一种神经退行性病变模型,在该模型中,慢性 rG4 的形成与蛋白稳态崩溃有关。这些形态学发现表明,进一步研究神经变性中的 RNA 结构是未来治疗和诊断的重要途径。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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