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Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement

Alzheimer’s disease (AD), Parkinson’s disease (PD), and amyotrophic lateral sclerosis (ALS) are neurodegenerative disorders characterized by a progressive degeneration of the central or peripheral nervous systems. A central role of the RNA metabolism has emerged in these diseases, concerning mRNAs p...

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Autores principales: Garofalo, Maria, Pandini, Cecilia, Bordoni, Matteo, Pansarasa, Orietta, Rey, Federica, Costa, Alfredo, Minafra, Brigida, Diamanti, Luca, Zucca, Susanna, Carelli, Stephana, Cereda, Cristina, Gagliardi, Stella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765024/
https://www.ncbi.nlm.nih.gov/pubmed/33327559
http://dx.doi.org/10.3390/ijms21249500
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author Garofalo, Maria
Pandini, Cecilia
Bordoni, Matteo
Pansarasa, Orietta
Rey, Federica
Costa, Alfredo
Minafra, Brigida
Diamanti, Luca
Zucca, Susanna
Carelli, Stephana
Cereda, Cristina
Gagliardi, Stella
author_facet Garofalo, Maria
Pandini, Cecilia
Bordoni, Matteo
Pansarasa, Orietta
Rey, Federica
Costa, Alfredo
Minafra, Brigida
Diamanti, Luca
Zucca, Susanna
Carelli, Stephana
Cereda, Cristina
Gagliardi, Stella
author_sort Garofalo, Maria
collection PubMed
description Alzheimer’s disease (AD), Parkinson’s disease (PD), and amyotrophic lateral sclerosis (ALS) are neurodegenerative disorders characterized by a progressive degeneration of the central or peripheral nervous systems. A central role of the RNA metabolism has emerged in these diseases, concerning mRNAs processing and non-coding RNAs biogenesis. We aimed to identify possible common grounds or differences in the dysregulated pathways of AD, PD, and ALS. To do so, we performed RNA-seq analysis to investigate the deregulation of both coding and long non-coding RNAs (lncRNAs) in ALS, AD, and PD patients and controls (CTRL) in peripheral blood mononuclear cells (PBMCs). A total of 293 differentially expressed (DE) lncRNAs and 87 mRNAs were found in ALS patients. In AD patients a total of 23 DE genes emerged, 19 protein coding genes and four lncRNAs. Through Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) analyses, we found common affected pathways and biological processes in ALS and AD. In PD patients only five genes were found to be DE. Our data brought to light the importance of lncRNAs and mRNAs regulation in three principal neurodegenerative disorders, offering starting points for new investigations on deregulated pathogenic mechanisms.
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spelling pubmed-77650242020-12-27 Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement Garofalo, Maria Pandini, Cecilia Bordoni, Matteo Pansarasa, Orietta Rey, Federica Costa, Alfredo Minafra, Brigida Diamanti, Luca Zucca, Susanna Carelli, Stephana Cereda, Cristina Gagliardi, Stella Int J Mol Sci Article Alzheimer’s disease (AD), Parkinson’s disease (PD), and amyotrophic lateral sclerosis (ALS) are neurodegenerative disorders characterized by a progressive degeneration of the central or peripheral nervous systems. A central role of the RNA metabolism has emerged in these diseases, concerning mRNAs processing and non-coding RNAs biogenesis. We aimed to identify possible common grounds or differences in the dysregulated pathways of AD, PD, and ALS. To do so, we performed RNA-seq analysis to investigate the deregulation of both coding and long non-coding RNAs (lncRNAs) in ALS, AD, and PD patients and controls (CTRL) in peripheral blood mononuclear cells (PBMCs). A total of 293 differentially expressed (DE) lncRNAs and 87 mRNAs were found in ALS patients. In AD patients a total of 23 DE genes emerged, 19 protein coding genes and four lncRNAs. Through Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) analyses, we found common affected pathways and biological processes in ALS and AD. In PD patients only five genes were found to be DE. Our data brought to light the importance of lncRNAs and mRNAs regulation in three principal neurodegenerative disorders, offering starting points for new investigations on deregulated pathogenic mechanisms. MDPI 2020-12-14 /pmc/articles/PMC7765024/ /pubmed/33327559 http://dx.doi.org/10.3390/ijms21249500 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Garofalo, Maria
Pandini, Cecilia
Bordoni, Matteo
Pansarasa, Orietta
Rey, Federica
Costa, Alfredo
Minafra, Brigida
Diamanti, Luca
Zucca, Susanna
Carelli, Stephana
Cereda, Cristina
Gagliardi, Stella
Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title_full Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title_fullStr Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title_full_unstemmed Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title_short Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement
title_sort alzheimer’s, parkinson’s disease and amyotrophic lateral sclerosis gene expression patterns divergence reveals different grade of rna metabolism involvement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765024/
https://www.ncbi.nlm.nih.gov/pubmed/33327559
http://dx.doi.org/10.3390/ijms21249500
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