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      Biological relevance and therapeutic potential of G-quadruplex structures in the human noncoding transcriptome

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      , ,
      Nucleic Acids Research
      Oxford University Press

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          Abstract

          Noncoding RNAs are functional transcripts that are not translated into proteins. They represent the largest portion of the human transcriptome and have been shown to regulate gene expression networks in both physiological and pathological cell conditions. Research in this field has made remarkable progress in the comprehension of how aberrations in noncoding RNA drive relevant disease-associated phenotypes; however, the biological role and mechanism of action of several noncoding RNAs still need full understanding. Besides fulfilling its function through sequence-based mechanisms, RNA can form complex secondary and tertiary structures which allow non-canonical interactions with proteins and/or other nucleic acids. In this context, the presence of G-quadruplexes in microRNAs and long noncoding RNAs is increasingly being reported. This evidence suggests a role for RNA G-quadruplexes in controlling microRNA biogenesis and mediating noncoding RNA interaction with biological partners, thus ultimately regulating gene expression. Here, we review the state of the art of G-quadruplexes in the noncoding transcriptome, with their structural and functional characterization. In light of the existence and further possible development of G-quadruplex binders that modulate G-quadruplex conformation and protein interactions, we also discuss the therapeutic potential of G-quadruplexes as targets to interfere with disease-associated noncoding RNAs.

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          MicroRNAs: genomics, biogenesis, mechanism, and function.

          MicroRNAs (miRNAs) are endogenous approximately 22 nt RNAs that can play important regulatory roles in animals and plants by targeting mRNAs for cleavage or translational repression. Although they escaped notice until relatively recently, miRNAs comprise one of the more abundant classes of gene regulatory molecules in multicellular organisms and likely influence the output of many protein-coding genes.
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            MicroRNA therapeutics: towards a new era for the management of cancer and other diseases

            MicroRNAs (miRNAs) are small non-coding RNAs that can modulate mRNA expression. Insights into the roles of miRNAs in development and disease have led to the development of new therapeutic approaches that are based on miRNA mimics or agents that inhibit their functions (antimiRs), and the first such approaches have entered the clinic. This Review discusses the role of different miRNAs in cancer and other diseases, and provides an overview of current miRNA therapeutics in the clinic.
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              Functional Classification and Experimental Dissection of Long Noncoding RNAs

              Over the last decade, it has been increasingly demonstrated that the genomes of many species are pervasively transcribed, resulting in the production of numerous long noncoding RNAs (lncRNAs). At the same time, it is now appreciated that many types of DNA regulatory elements, such as enhancers and promoters, regularly initiate bidirectional transcription. Thus, discerning functional noncoding transcripts from a vast transcriptome is a paramount priority, and challenge, for the lncRNA field. In this review, we aim to provide a conceptual and experimental framework for classifying and elucidating lncRNA function. We categorize lncRNA loci into those that regulate gene expression in cis versus those that perform functions in trans , and propose an experimental approach to dissect lncRNA activity based on these classifications. These strategies to further understand lncRNAs promise to reveal new and unanticipated biology, with great potential to advance our understanding of normal physiology and disease.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                19 April 2021
                15 March 2021
                15 March 2021
                : 49
                : 7
                : 3617-3633
                Affiliations
                Department of Biosciences, University of Milan , via G. Celoria 26, 20133 Milano, Italy
                Department of Molecular Medicine, University of Padua , via A. Gabelli 63, 35121 Padova, Italy
                Department of Biosciences, University of Milan , via G. Celoria 26, 20133 Milano, Italy
                Author notes
                To whom correspondence should be addressed. Tel: +39 0250314954; Email: paolo.gandellini@ 123456unimi.it
                Correspondence may also be addressed to Sara N. Richter. Email: sara.richter@ 123456unipd.it
                Author information
                https://orcid.org/0000-0002-3965-9334
                https://orcid.org/0000-0002-5446-9029
                https://orcid.org/0000-0002-7811-3377
                Article
                gkab127
                10.1093/nar/gkab127
                8053107
                33721024
                d530af38-008d-4608-b33b-e9a355be9590
                © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 15 February 2021
                : 10 February 2021
                : 16 October 2020
                Page count
                Pages: 17
                Funding
                Funded by: Italian Ministry of Health;
                Award ID: GR-2013-02355625
                Funded by: Cariplo Foundation, DOI 10.13039/501100002803;
                Award ID: 2015-0866
                Funded by: AIRC Foundation;
                Award ID: 21850
                Award ID: 24325
                Categories
                AcademicSubjects/SCI00010
                Survey and Summary

                Genetics
                Genetics

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