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Noncoding RNA in age-related cardiovascular diseases

Eukaryotic gene expression is tightly regulated transcriptionally and post-transcriptionally by a host of noncoding (nc)RNAs. The best-studied class of short ncRNAs, microRNAs, mainly repress gene expression post-transcriptionally. Long noncoding (lnc)RNAs, which comprise RNAs differing widely in le...

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Detalles Bibliográficos
Autores principales: Greco, Simona, Gorospe, Myriam, Martelli, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509469/
https://www.ncbi.nlm.nih.gov/pubmed/25640162
http://dx.doi.org/10.1016/j.yjmcc.2015.01.011
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author Greco, Simona
Gorospe, Myriam
Martelli, Fabio
author_facet Greco, Simona
Gorospe, Myriam
Martelli, Fabio
author_sort Greco, Simona
collection PubMed
description Eukaryotic gene expression is tightly regulated transcriptionally and post-transcriptionally by a host of noncoding (nc)RNAs. The best-studied class of short ncRNAs, microRNAs, mainly repress gene expression post-transcriptionally. Long noncoding (lnc)RNAs, which comprise RNAs differing widely in length and function, can regulate gene transcription as well as post-transcriptional mRNA fate. Collectively, ncRNAs affect a broad range of age-related physiologic deteriorations and pathologies, including reduced cardiovascular vigor and age-associated cardiovascular disease. This review presents an update of our understanding of regulatory ncRNAs contributing to cardiovascular health and disease as a function of advancing age. We will discuss (1) regulatory ncRNAs that control aging-associated cardiovascular homeostasis and disease, (2) the concepts, approaches, and methodologies needed to study regulatory ncRNAs in cardiovascular aging and (3) the challenges and opportunities that age-associated regulatory ncRNAs present in cardiovascular physiology and pathology. This article is part of a Special Issue entitled “CV Aging”.
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spelling pubmed-55094692017-07-13 Noncoding RNA in age-related cardiovascular diseases Greco, Simona Gorospe, Myriam Martelli, Fabio J Mol Cell Cardiol Article Eukaryotic gene expression is tightly regulated transcriptionally and post-transcriptionally by a host of noncoding (nc)RNAs. The best-studied class of short ncRNAs, microRNAs, mainly repress gene expression post-transcriptionally. Long noncoding (lnc)RNAs, which comprise RNAs differing widely in length and function, can regulate gene transcription as well as post-transcriptional mRNA fate. Collectively, ncRNAs affect a broad range of age-related physiologic deteriorations and pathologies, including reduced cardiovascular vigor and age-associated cardiovascular disease. This review presents an update of our understanding of regulatory ncRNAs contributing to cardiovascular health and disease as a function of advancing age. We will discuss (1) regulatory ncRNAs that control aging-associated cardiovascular homeostasis and disease, (2) the concepts, approaches, and methodologies needed to study regulatory ncRNAs in cardiovascular aging and (3) the challenges and opportunities that age-associated regulatory ncRNAs present in cardiovascular physiology and pathology. This article is part of a Special Issue entitled “CV Aging”. 2015-01-29 2015-06 /pmc/articles/PMC5509469/ /pubmed/25640162 http://dx.doi.org/10.1016/j.yjmcc.2015.01.011 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Greco, Simona
Gorospe, Myriam
Martelli, Fabio
Noncoding RNA in age-related cardiovascular diseases
title Noncoding RNA in age-related cardiovascular diseases
title_full Noncoding RNA in age-related cardiovascular diseases
title_fullStr Noncoding RNA in age-related cardiovascular diseases
title_full_unstemmed Noncoding RNA in age-related cardiovascular diseases
title_short Noncoding RNA in age-related cardiovascular diseases
title_sort noncoding rna in age-related cardiovascular diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509469/
https://www.ncbi.nlm.nih.gov/pubmed/25640162
http://dx.doi.org/10.1016/j.yjmcc.2015.01.011
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