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microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome
microRNAs are a type of small non-coding RNAs which play important roles in post-transcriptional gene regulation, and the characterization of microRNA expression profiling in peripheral blood mononuclear cells (PBMCs) from patients with Klinefelter syndrome requires further investigation. In this st...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493739/ https://www.ncbi.nlm.nih.gov/pubmed/23226734 http://dx.doi.org/10.3892/etm.2012.682 |
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author | SUI, WEIGUO OU, MINGLIN CHEN, JIEJING LI, HUAN LIN, HUA ZHANG, YUE LI, WUXIAN XUE, WEN TANG, DONGE GONG, WEIWEI ZHANG, RUOHAN LI, FENGYAN DAI, YONG |
author_facet | SUI, WEIGUO OU, MINGLIN CHEN, JIEJING LI, HUAN LIN, HUA ZHANG, YUE LI, WUXIAN XUE, WEN TANG, DONGE GONG, WEIWEI ZHANG, RUOHAN LI, FENGYAN DAI, YONG |
author_sort | SUI, WEIGUO |
collection | PubMed |
description | microRNAs are a type of small non-coding RNAs which play important roles in post-transcriptional gene regulation, and the characterization of microRNA expression profiling in peripheral blood mononuclear cells (PBMCs) from patients with Klinefelter syndrome requires further investigation. In this study, PBMCs were obtained from patients with Klinefelter syndrome and normal controls. After preparation of small RNA libraries, the two groups of samples were sequenced simultaneously using next generation high-throughput sequencing technology, and novel and known microRNAs were analyzed. A total of 9,772,392 and 9,717,633 small RNA reads were obtained; 8,014,466 (82.01%) and 8,104,423 (83.40%) genome-matched reads, 64 and 49 novel microRNAs were identified in the library of Klinefelter syndrome and the library of healthy controls, respectively. There were 71 known microRNAs with differential expression levels between the two libraries. Clustering of over-represented gene ontology (GO) classes in predicted targets of novel microRNAs in the Klinefelter syndrome library showed that the most significant GO terms were genes involved in the endomembrane system, nucleotide binding and kinase activity. Our data revealed that there are a large number of microRNAs deregulated in PBMCs taken from patients with Klinefelter syndrome, of which certain novel and known microRNAs may be involved in the pathological process of Klinefelter syndrome. Further studies are necessary to determine the roles of microRNAs in the pathological process of Klinefelter syndrome in the future. |
format | Online Article Text |
id | pubmed-3493739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-34937392012-12-06 microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome SUI, WEIGUO OU, MINGLIN CHEN, JIEJING LI, HUAN LIN, HUA ZHANG, YUE LI, WUXIAN XUE, WEN TANG, DONGE GONG, WEIWEI ZHANG, RUOHAN LI, FENGYAN DAI, YONG Exp Ther Med Articles microRNAs are a type of small non-coding RNAs which play important roles in post-transcriptional gene regulation, and the characterization of microRNA expression profiling in peripheral blood mononuclear cells (PBMCs) from patients with Klinefelter syndrome requires further investigation. In this study, PBMCs were obtained from patients with Klinefelter syndrome and normal controls. After preparation of small RNA libraries, the two groups of samples were sequenced simultaneously using next generation high-throughput sequencing technology, and novel and known microRNAs were analyzed. A total of 9,772,392 and 9,717,633 small RNA reads were obtained; 8,014,466 (82.01%) and 8,104,423 (83.40%) genome-matched reads, 64 and 49 novel microRNAs were identified in the library of Klinefelter syndrome and the library of healthy controls, respectively. There were 71 known microRNAs with differential expression levels between the two libraries. Clustering of over-represented gene ontology (GO) classes in predicted targets of novel microRNAs in the Klinefelter syndrome library showed that the most significant GO terms were genes involved in the endomembrane system, nucleotide binding and kinase activity. Our data revealed that there are a large number of microRNAs deregulated in PBMCs taken from patients with Klinefelter syndrome, of which certain novel and known microRNAs may be involved in the pathological process of Klinefelter syndrome. Further studies are necessary to determine the roles of microRNAs in the pathological process of Klinefelter syndrome in the future. D.A. Spandidos 2012-11 2012-08-24 /pmc/articles/PMC3493739/ /pubmed/23226734 http://dx.doi.org/10.3892/etm.2012.682 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles SUI, WEIGUO OU, MINGLIN CHEN, JIEJING LI, HUAN LIN, HUA ZHANG, YUE LI, WUXIAN XUE, WEN TANG, DONGE GONG, WEIWEI ZHANG, RUOHAN LI, FENGYAN DAI, YONG microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title | microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title_full | microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title_fullStr | microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title_full_unstemmed | microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title_short | microRNA expression profile of peripheral blood mononuclear cells of Klinefelter syndrome |
title_sort | microrna expression profile of peripheral blood mononuclear cells of klinefelter syndrome |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493739/ https://www.ncbi.nlm.nih.gov/pubmed/23226734 http://dx.doi.org/10.3892/etm.2012.682 |
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