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阿尔茨海默病多个脑区的 m6A 调节因子全景图。

The Landscape of m6A Regulators in Multiple Brain Regions of Alzheimer's Disease.

机构信息

Department of Biochemistry and Molecular Biology, Harbin Medical University, No. 157 Harbin health care road, Nangang District, Harbin, China.

Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Mol Neurobiol. 2023 Sep;60(9):5184-5198. doi: 10.1007/s12035-023-03409-5. Epub 2023 Jun 5.

Abstract

Alzheimer's disease research has been conducted for many years, yet no effective cure methods have been found. N6-methyladenosine (m6A) RNA methylation, an essential post-transcriptional regulation mechanism, has been discovered to affect essential neurobiological processes, such as brain cell development and aging, which are closely related to neurodegenerative diseases such as Alzheimer's disease. The relationship between Alzheimer's disease and the m6A mechanism still needs further investigation. Our work evaluated the alteration profile of m6A regulators and their influences on Alzheimer's disease in 4 brain regions: the postcentral gyrus, superior frontal gyrus, hippocampus, and entorhinal cortex. We found that the expression levels of the m6A regulators FTO, ELAVL1, and YTHDF2 were altered in Alzheimer's disease and were related to pathological development and cognitive levels. We also assessed AD-related biological processes influenced by m6A regulators via GSEA and GSVA method. Biological Processes Gene Ontology terms including memory, cognition, and synapse-signaling were found to potentially be affected by m6A regulators in AD. We also found different m6A modification patterns in AD samples among different brain regions, mainly due to differences in m6A readers. Finally, we further evaluated the importance of AD-related regulators based on the WGCNA method, assessed their potential targets based on correlation relationships, and constructed diagnostic models in 3 of all 4 regions using hub regulators, including FTO, YTHDC1, YTHDC2, etc., and their potential targets. This work aims to provide a reference for the follow-up study of m6A and Alzheimer's disease.

摘要

阿尔茨海默病的研究已经进行了多年,但仍未找到有效的治疗方法。N6-甲基腺苷(m6A)RNA 甲基化是一种重要的转录后调控机制,已被发现影响关键的神经生物学过程,如脑细胞的发育和衰老,这些过程与阿尔茨海默病等神经退行性疾病密切相关。阿尔茨海默病与 m6A 机制之间的关系仍需要进一步研究。我们的工作评估了 4 个脑区(中央后回、额上回、海马和内嗅皮层)中 m6A 调节因子的改变谱及其对阿尔茨海默病的影响。我们发现,m6A 调节因子 FTO、ELAVL1 和 YTHDF2 的表达水平在阿尔茨海默病中发生改变,与病理发展和认知水平有关。我们还通过 GSEA 和 GSVA 方法评估了 m6A 调节因子对 AD 相关生物学过程的影响。包括记忆、认知和突触信号在内的生物学过程基因本体论术语可能受到 AD 中 m6A 调节因子的影响。我们还发现,不同脑区的 AD 样本中的 m6A 修饰模式不同,主要是由于 m6A 读取器的差异。最后,我们还基于 WGCNA 方法进一步评估了 AD 相关调节因子的重要性,根据相关性评估了它们的潜在靶点,并在 4 个区域中的 3 个区域中使用 hub 调节因子(包括 FTO、YTHDC1、YTHDC2 等)及其潜在靶点构建了诊断模型。这项工作旨在为 m6A 和阿尔茨海默病的后续研究提供参考。

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