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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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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. |
format | Online Article Text |
id | pubmed-7854456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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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