Cargando…
LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury
The study aimed to investigate time‐course transcriptomes in myocardial ischaemia reperfusion injury (IRI) via RNA‐Seq. Transcriptomes of 10 samples derived from patients with acute ST‐segment elevation myocardial infarction (ASTEMI) who were assigned to percutaneous coronary intervention (PCI), wer...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378211/ https://www.ncbi.nlm.nih.gov/pubmed/30657634 http://dx.doi.org/10.1111/jcmm.14163 |
_version_ | 1783395886768848896 |
---|---|
author | Liu, Hongying Xu, Danping Zhong, Xin Xu, Dongsheng Chen, Geng Ge, Junbo Li, Hua |
author_facet | Liu, Hongying Xu, Danping Zhong, Xin Xu, Dongsheng Chen, Geng Ge, Junbo Li, Hua |
author_sort | Liu, Hongying |
collection | PubMed |
description | The study aimed to investigate time‐course transcriptomes in myocardial ischaemia reperfusion injury (IRI) via RNA‐Seq. Transcriptomes of 10 samples derived from patients with acute ST‐segment elevation myocardial infarction (ASTEMI) who were assigned to percutaneous coronary intervention (PCI), were sequenced at the time of 0 (before PCI), 2, 12, 24 and 72 hours after PCI, respectively. Using the genefilter package in r, wgcna and stem, different expression lncRNA (DEL) and mRNA (DEM) were analysed. Out of 756 mRNAs and 206 lncRNAs shared by enrolled patients, 135 RNAs were screened to be significantly associated with the IRI. Furthermore, combined with lncRNA‐mRNA, lncRNA‐miRNA and miRNA‐mRNA network, 51 RNAs and 131 relationship pairs were ascertained in the competing endogenous RNAs (ceRNA) network. Among these nodes, SH2D3C and GTF2H4 were significantly enriched in cellular response to stress and their interaction module were isolated from functional ceRNA network. Subsequently, their critical role was confirmed via down‐regulation of SH2D3C and GTF2H4 expression in vitro model. These results identified that lncRNA‐mRNA ceRNA network, associated significantly with IRI, functioned as critical regulative pivotal roles after PCI‐AMI, and SH2D3C and GTF2H4 may be the most responsive transcriptional regulator in the early‐phase of IRI. |
format | Online Article Text |
id | pubmed-6378211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63782112019-03-01 LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury Liu, Hongying Xu, Danping Zhong, Xin Xu, Dongsheng Chen, Geng Ge, Junbo Li, Hua J Cell Mol Med Short Communications The study aimed to investigate time‐course transcriptomes in myocardial ischaemia reperfusion injury (IRI) via RNA‐Seq. Transcriptomes of 10 samples derived from patients with acute ST‐segment elevation myocardial infarction (ASTEMI) who were assigned to percutaneous coronary intervention (PCI), were sequenced at the time of 0 (before PCI), 2, 12, 24 and 72 hours after PCI, respectively. Using the genefilter package in r, wgcna and stem, different expression lncRNA (DEL) and mRNA (DEM) were analysed. Out of 756 mRNAs and 206 lncRNAs shared by enrolled patients, 135 RNAs were screened to be significantly associated with the IRI. Furthermore, combined with lncRNA‐mRNA, lncRNA‐miRNA and miRNA‐mRNA network, 51 RNAs and 131 relationship pairs were ascertained in the competing endogenous RNAs (ceRNA) network. Among these nodes, SH2D3C and GTF2H4 were significantly enriched in cellular response to stress and their interaction module were isolated from functional ceRNA network. Subsequently, their critical role was confirmed via down‐regulation of SH2D3C and GTF2H4 expression in vitro model. These results identified that lncRNA‐mRNA ceRNA network, associated significantly with IRI, functioned as critical regulative pivotal roles after PCI‐AMI, and SH2D3C and GTF2H4 may be the most responsive transcriptional regulator in the early‐phase of IRI. John Wiley and Sons Inc. 2019-01-18 2019-03 /pmc/articles/PMC6378211/ /pubmed/30657634 http://dx.doi.org/10.1111/jcmm.14163 Text en © 2019 The Authors Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Liu, Hongying Xu, Danping Zhong, Xin Xu, Dongsheng Chen, Geng Ge, Junbo Li, Hua LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title | LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title_full | LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title_fullStr | LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title_full_unstemmed | LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title_short | LncRNA‐mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury |
title_sort | lncrna‐mrna competing endogenous rna network depicts transcriptional regulation in ischaemia reperfusion injury |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378211/ https://www.ncbi.nlm.nih.gov/pubmed/30657634 http://dx.doi.org/10.1111/jcmm.14163 |
work_keys_str_mv | AT liuhongying lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT xudanping lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT zhongxin lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT xudongsheng lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT chengeng lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT gejunbo lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury AT lihua lncrnamrnacompetingendogenousrnanetworkdepictstranscriptionalregulationinischaemiareperfusioninjury |