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What microRNAs could tell us about the human X chromosome

MicroRNAs (miRNA) are small-non coding RNAs endowed with great regulatory power, thus playing key roles not only in almost all physiological pathways, but also in the pathogenesis of several diseases. Surprisingly, genomic distribution analysis revealed the highest density of miRNA sequences on the...

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Autores principales: Di Palo, Armando, Siniscalchi, Chiara, Salerno, Mariacarolina, Russo, Aniello, Gravholt, Claus Højbjerg, Potenza, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854456/
https://www.ncbi.nlm.nih.gov/pubmed/32356180
http://dx.doi.org/10.1007/s00018-020-03526-7
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author Di Palo, Armando
Siniscalchi, Chiara
Salerno, Mariacarolina
Russo, Aniello
Gravholt, Claus Højbjerg
Potenza, Nicoletta
author_facet Di Palo, Armando
Siniscalchi, Chiara
Salerno, Mariacarolina
Russo, Aniello
Gravholt, Claus Højbjerg
Potenza, Nicoletta
author_sort Di Palo, Armando
collection PubMed
description MicroRNAs (miRNA) are small-non coding RNAs endowed with great regulatory power, thus playing key roles not only in almost all physiological pathways, but also in the pathogenesis of several diseases. Surprisingly, genomic distribution analysis revealed the highest density of miRNA sequences on the X chromosome; this evolutionary conserved mammalian feature equips females with a larger miRNA machinery than males. However, miRNAs contribution to some X-related conditions, properties or functions is still poorly explored. With the aim to support and focus research in the field, this review analyzes the literature and databases about X-linked miRNAs, trying to understand how miRNAs could contribute to emerging gender-biased functions and pathological mechanisms, such as immunity and cancer. A fine map of miRNA sequences on the X chromosome is reported, and their known functions are discussed; in addition, bioinformatics functional analyses of the whole X-linked miRNA targetome (predicted and validated) were performed. The emerging scenario points to different gaps in the knowledge that should be filled with future experimental investigations, also in terms of possible implications and pathological perspectives for X chromosome aneuploidy syndromes, such as Turner and Klinefelter syndromes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00018-020-03526-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-78544562021-02-11 What microRNAs could tell us about the human X chromosome Di Palo, Armando Siniscalchi, Chiara Salerno, Mariacarolina Russo, Aniello Gravholt, Claus Højbjerg Potenza, Nicoletta Cell Mol Life Sci Review MicroRNAs (miRNA) are small-non coding RNAs endowed with great regulatory power, thus playing key roles not only in almost all physiological pathways, but also in the pathogenesis of several diseases. Surprisingly, genomic distribution analysis revealed the highest density of miRNA sequences on the X chromosome; this evolutionary conserved mammalian feature equips females with a larger miRNA machinery than males. However, miRNAs contribution to some X-related conditions, properties or functions is still poorly explored. With the aim to support and focus research in the field, this review analyzes the literature and databases about X-linked miRNAs, trying to understand how miRNAs could contribute to emerging gender-biased functions and pathological mechanisms, such as immunity and cancer. A fine map of miRNA sequences on the X chromosome is reported, and their known functions are discussed; in addition, bioinformatics functional analyses of the whole X-linked miRNA targetome (predicted and validated) were performed. The emerging scenario points to different gaps in the knowledge that should be filled with future experimental investigations, also in terms of possible implications and pathological perspectives for X chromosome aneuploidy syndromes, such as Turner and Klinefelter syndromes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00018-020-03526-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-04-30 2020 /pmc/articles/PMC7854456/ /pubmed/32356180 http://dx.doi.org/10.1007/s00018-020-03526-7 Text en © The Author(s) 2020, corrected publication 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Di Palo, Armando
Siniscalchi, Chiara
Salerno, Mariacarolina
Russo, Aniello
Gravholt, Claus Højbjerg
Potenza, Nicoletta
What microRNAs could tell us about the human X chromosome
title What microRNAs could tell us about the human X chromosome
title_full What microRNAs could tell us about the human X chromosome
title_fullStr What microRNAs could tell us about the human X chromosome
title_full_unstemmed What microRNAs could tell us about the human X chromosome
title_short What microRNAs could tell us about the human X chromosome
title_sort what micrornas could tell us about the human x chromosome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854456/
https://www.ncbi.nlm.nih.gov/pubmed/32356180
http://dx.doi.org/10.1007/s00018-020-03526-7
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