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...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Hongying, Xu, Danping, Zhong, Xin, Xu, Dongsheng, Chen, Geng, Ge, Junbo, Li, Hua
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