INTRODUCTIONAs the world population ages, new molecular targets in aging and Alzheimers 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.
RESULTSWe 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.
DISCUSSIONCombined 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 drives proteostasis collapse. These morphological findings suggest that further investigation of RNA structure in neurodegeneration is a critical avenue for future treatments and diagnoses.
Longevity Relevance Analysis
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The paper explores the role of RNA G-quadruplexes in the context of aging and Alzheimer's Disease, suggesting a potential mechanism that could contribute to neurodegeneration. While it presents interesting findings regarding the relationship between rG4s and tau aggregation, it primarily focuses on a specific molecular target rather than addressing the root causes of aging or proposing a broader strategy for lifespan extension. Thus, it represents solid research but with limited impact on the overall field of longevity.