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Competing Endogenous RNA: The Key to Posttranscriptional Regulation

Competing endogenous RNA, ceRNA, vie with messenger RNAs (mRNAs) for microRNAs (miRNAs) with shared miRNAs responses elements (MREs) and act as modulator of miRNA by influencing the available level of miRNA. It has recently been discovered that, apart from protein-coding ceRNAs, pseudogenes, long no...

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Autores principales: Sen, Rituparno, Ghosal, Suman, Das, Shaoli, Balti, Subrata, Chakrabarti, Jayprokas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929601/
https://www.ncbi.nlm.nih.gov/pubmed/24672386
http://dx.doi.org/10.1155/2014/896206
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author Sen, Rituparno
Ghosal, Suman
Das, Shaoli
Balti, Subrata
Chakrabarti, Jayprokas
author_facet Sen, Rituparno
Ghosal, Suman
Das, Shaoli
Balti, Subrata
Chakrabarti, Jayprokas
author_sort Sen, Rituparno
collection PubMed
description Competing endogenous RNA, ceRNA, vie with messenger RNAs (mRNAs) for microRNAs (miRNAs) with shared miRNAs responses elements (MREs) and act as modulator of miRNA by influencing the available level of miRNA. It has recently been discovered that, apart from protein-coding ceRNAs, pseudogenes, long noncoding RNAs (lncRNAs), and circular RNAs act as miRNA “sponges” by sharing common MRE, inhibiting normal miRNA targeting activity on mRNA. These MRE sharing elements form the posttranscriptional ceRNA network to regulate mRNA expression. ceRNAs are widely implicated in many biological processes. Recent studies have identified ceRNAs associated with a number of diseases including cancer. This brief review focuses on the molecular mechanism of ceRNA as part of the complex post-transcriptional regulatory circuit in cell and the impact of ceRNAs in development and disease.
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spelling pubmed-39296012014-03-26 Competing Endogenous RNA: The Key to Posttranscriptional Regulation Sen, Rituparno Ghosal, Suman Das, Shaoli Balti, Subrata Chakrabarti, Jayprokas ScientificWorldJournal Review Article Competing endogenous RNA, ceRNA, vie with messenger RNAs (mRNAs) for microRNAs (miRNAs) with shared miRNAs responses elements (MREs) and act as modulator of miRNA by influencing the available level of miRNA. It has recently been discovered that, apart from protein-coding ceRNAs, pseudogenes, long noncoding RNAs (lncRNAs), and circular RNAs act as miRNA “sponges” by sharing common MRE, inhibiting normal miRNA targeting activity on mRNA. These MRE sharing elements form the posttranscriptional ceRNA network to regulate mRNA expression. ceRNAs are widely implicated in many biological processes. Recent studies have identified ceRNAs associated with a number of diseases including cancer. This brief review focuses on the molecular mechanism of ceRNA as part of the complex post-transcriptional regulatory circuit in cell and the impact of ceRNAs in development and disease. Hindawi Publishing Corporation 2014-02-02 /pmc/articles/PMC3929601/ /pubmed/24672386 http://dx.doi.org/10.1155/2014/896206 Text en Copyright © 2014 Rituparno Sen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sen, Rituparno
Ghosal, Suman
Das, Shaoli
Balti, Subrata
Chakrabarti, Jayprokas
Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title_full Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title_fullStr Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title_full_unstemmed Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title_short Competing Endogenous RNA: The Key to Posttranscriptional Regulation
title_sort competing endogenous rna: the key to posttranscriptional regulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929601/
https://www.ncbi.nlm.nih.gov/pubmed/24672386
http://dx.doi.org/10.1155/2014/896206
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