Suppr超能文献

阿尔茨海默病中失调的长链非编码RNA的鉴定:海马体和梭状回RNA测序数据集的综合基因共表达网络分析

Identification of deregulated lncRNAs in Alzheimer's disease: an integrated gene co-expression network analysis of hippocampus and fusiform gyrus RNA-seq datasets.

作者信息

Filomena Ermes, Picardi Ernesto, Tullo Apollonia, Pesole Graziano, D'Erchia Anna Maria

机构信息

Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Bari, Italy.

Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Bari, Italy.

出版信息

Front Aging Neurosci. 2024 Jul 17;16:1437278. doi: 10.3389/fnagi.2024.1437278. eCollection 2024.

Abstract

INTRODUCTION

The deregulation of lncRNAs expression has been associated with neuronal damage in Alzheimer's disease (AD), but how or whether they can influence its onset is still unknown. We investigated 2 RNA-seq datasets consisting, respectively, of the hippocampal and fusiform gyrus transcriptomic profile of AD patients, matched with non-demented controls.

METHODS

We performed a differential expression analysis, a gene correlation network analysis (WGCNA) and a pathway enrichment analysis of two RNA-seq datasets.

RESULTS

We found deregulated lncRNAs in common between hippocampus and fusiform gyrus and deregulated gene groups associated to functional pathways related to neurotransmission and memory consolidation. lncRNAs, co-expressed with known AD-related coding genes, were identified from the prioritized modules of both brain regions.

DISCUSSION

We found common deregulated lncRNAs in the AD hippocampus and fusiform gyrus, that could be considered common signatures of AD pathogenesis, providing an important source of information for understanding the molecular changes of AD.

摘要

引言

长链非编码RNA(lncRNAs)表达失调与阿尔茨海默病(AD)中的神经元损伤有关,但它们如何影响或是否能影响AD的发病仍不清楚。我们研究了两个RNA测序数据集,分别由AD患者的海马体和梭状回转录组图谱以及与之匹配的非痴呆对照组成。

方法

我们对两个RNA测序数据集进行了差异表达分析、基因相关网络分析(WGCNA)和通路富集分析。

结果

我们发现海马体和梭状回中存在共同失调的lncRNAs,以及与神经传递和记忆巩固相关功能通路的失调基因组。从两个脑区的优先模块中鉴定出与已知AD相关编码基因共表达的lncRNAs。

讨论

我们在AD海马体和梭状回中发现了共同失调的lncRNAs,可将其视为AD发病机制的共同特征,为理解AD的分子变化提供了重要信息来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04cb/11288953/0e3ea566acaf/fnagi-16-1437278-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验