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Identification of deregulated lncRNAs in Alzheimer's disease: an integrated gene co-expression network analysis of hippocampus and fusiform gyrus RNA-seq datasets.
Filomena, Ermes; Picardi, Ernesto; Tullo, Apollonia; Pesole, Graziano; D'Erchia, Anna Maria.
Afiliação
  • Filomena E; Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Bari, Italy.
  • Picardi E; Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Bari, Italy.
  • Tullo A; Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Bari, Italy.
  • Pesole G; Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Bari, Italy.
  • D'Erchia AM; Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Bari, Italy.
Front Aging Neurosci ; 16: 1437278, 2024.
Article em En | MEDLINE | ID: mdl-39086756
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article