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Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression
Intronic miRNAs, residing in intronic regions of host genes, are thought to be co-transcribed from their host genes and present consistent expression patterns with host genes. Recent studies reported a few intronic miRNAs with discordant expression with their host genes. We therefore aimed to unders...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715526/ https://www.ncbi.nlm.nih.gov/pubmed/29209147 http://dx.doi.org/10.7150/ijbs.20836 |
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author | Sun, Yulin Ji, Fubo Kumar, Mia R Zheng, Xin Xiao, Yi Liu, Niya Shi, Jiong Wong, Linda Forgues, Marshonna Qin, Lun-Xiu Tang, Zhao-You Zhao, Xiaohang Wang, Xin Wei Ji, Junfang |
author_facet | Sun, Yulin Ji, Fubo Kumar, Mia R Zheng, Xin Xiao, Yi Liu, Niya Shi, Jiong Wong, Linda Forgues, Marshonna Qin, Lun-Xiu Tang, Zhao-You Zhao, Xiaohang Wang, Xin Wei Ji, Junfang |
author_sort | Sun, Yulin |
collection | PubMed |
description | Intronic miRNAs, residing in intronic regions of host genes, are thought to be co-transcribed from their host genes and present consistent expression patterns with host genes. Recent studies reported a few intronic miRNAs with discordant expression with their host genes. We therefore aimed to understand the expression pattern of intronic miRNAs and their host genes in hepatocellular carcinoma (HCC) and reveal possible associated molecular mechanisms. Our genome wide integration analysis of miRNA and mRNA transcriptomes, in three dataset from 550 patients with HCC, found that a large amount of miRNA-host gene pairs were discordantly expressed. Consistent results were also revealed in 775 breast cancer patients. Further, most of HCC-related intronic miRNAs were predicted to have distinct upstream regulators and independent proximal promoter signals from host genes. The discordant expression of representative pairs, miR-26s/CTDSPs, was validated experimentally. We have also identified the independent transcriptional start site, promoter signal, and transcriptional factor of miR-26b from its host gene. Collectively, discordant expression of intronic miRNAs and their host genes was relatively ubiquitous and the intronic miRNA “independent transcription” may partially contribute to such a phenotype. |
format | Online Article Text |
id | pubmed-5715526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-57155262017-12-05 Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression Sun, Yulin Ji, Fubo Kumar, Mia R Zheng, Xin Xiao, Yi Liu, Niya Shi, Jiong Wong, Linda Forgues, Marshonna Qin, Lun-Xiu Tang, Zhao-You Zhao, Xiaohang Wang, Xin Wei Ji, Junfang Int J Biol Sci Research Paper Intronic miRNAs, residing in intronic regions of host genes, are thought to be co-transcribed from their host genes and present consistent expression patterns with host genes. Recent studies reported a few intronic miRNAs with discordant expression with their host genes. We therefore aimed to understand the expression pattern of intronic miRNAs and their host genes in hepatocellular carcinoma (HCC) and reveal possible associated molecular mechanisms. Our genome wide integration analysis of miRNA and mRNA transcriptomes, in three dataset from 550 patients with HCC, found that a large amount of miRNA-host gene pairs were discordantly expressed. Consistent results were also revealed in 775 breast cancer patients. Further, most of HCC-related intronic miRNAs were predicted to have distinct upstream regulators and independent proximal promoter signals from host genes. The discordant expression of representative pairs, miR-26s/CTDSPs, was validated experimentally. We have also identified the independent transcriptional start site, promoter signal, and transcriptional factor of miR-26b from its host gene. Collectively, discordant expression of intronic miRNAs and their host genes was relatively ubiquitous and the intronic miRNA “independent transcription” may partially contribute to such a phenotype. Ivyspring International Publisher 2017-11-01 /pmc/articles/PMC5715526/ /pubmed/29209147 http://dx.doi.org/10.7150/ijbs.20836 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Sun, Yulin Ji, Fubo Kumar, Mia R Zheng, Xin Xiao, Yi Liu, Niya Shi, Jiong Wong, Linda Forgues, Marshonna Qin, Lun-Xiu Tang, Zhao-You Zhao, Xiaohang Wang, Xin Wei Ji, Junfang Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title | Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title_full | Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title_fullStr | Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title_full_unstemmed | Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title_short | Transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic miRNA-host gene pairs in expression |
title_sort | transcriptome integration analysis in hepatocellular carcinoma reveals discordant intronic mirna-host gene pairs in expression |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715526/ https://www.ncbi.nlm.nih.gov/pubmed/29209147 http://dx.doi.org/10.7150/ijbs.20836 |
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