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Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect

Objectives: To explore and validate the differential expression of circRNAs in the myocardium of congenital ventricular septal defect (VSD) and to explore a new avenue of research regarding the pathological mechanisms of VSD. Methods: We detected circRNAs expression profiles in heart tissues taken f...

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Autores principales: Liu, Heng, Hu, Yin, Zhuang, Bin, Yin, Jing, Chen, Xiao-Hui, Wang, Juan, Li, Meng-Meng, Xu, Jing, Wang, Xing-Yun, Yu, Zhang-Bin, Han, Shu-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001411/
https://www.ncbi.nlm.nih.gov/pubmed/29910675
http://dx.doi.org/10.7150/ijms.21660
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author Liu, Heng
Hu, Yin
Zhuang, Bin
Yin, Jing
Chen, Xiao-Hui
Wang, Juan
Li, Meng-Meng
Xu, Jing
Wang, Xing-Yun
Yu, Zhang-Bin
Han, Shu-Ping
author_facet Liu, Heng
Hu, Yin
Zhuang, Bin
Yin, Jing
Chen, Xiao-Hui
Wang, Juan
Li, Meng-Meng
Xu, Jing
Wang, Xing-Yun
Yu, Zhang-Bin
Han, Shu-Ping
author_sort Liu, Heng
collection PubMed
description Objectives: To explore and validate the differential expression of circRNAs in the myocardium of congenital ventricular septal defect (VSD) and to explore a new avenue of research regarding the pathological mechanisms of VSD. Methods: We detected circRNAs expression profiles in heart tissues taken from six aborted fetuses with VSD and normal group using circRNA microarray. Some differentially expressed circRNAs were studied by bioinformatics analysis. Finally, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was performed to confirm these results. Results: This study found abundant circRNAs in the myocardium taken from individuals in the normal group and the VSD group. After that, totally 6234 differentially expressed circRNAs between the normal group and the VSD group were confirmed (Fold change ≥ 2.0; p < 0.05). Then, this research carried out bioinformatics analysis and predicted the potential biological functions of circRNAs. Finally, the over-expression of hsa_circRNA_002086 and under-expression of hsa_circRNA_007878, hsa_circRNA_100709, hsa_circRNA_101965, hsa_circRNA_402565 were further validated by qRT-PCR. Conclusions: There is a significant difference in expression of the circRNA in cardiac tissue from VSD group compared to the normal group. Combined with the microarray results and previous researches, circRNAs may contribute to the occurrence of VSD by acting as miRNA sponges or by binding proteins, these possible roles for circRNAs in VSD require elucidation in additional studies.
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spelling pubmed-60014112018-06-15 Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect Liu, Heng Hu, Yin Zhuang, Bin Yin, Jing Chen, Xiao-Hui Wang, Juan Li, Meng-Meng Xu, Jing Wang, Xing-Yun Yu, Zhang-Bin Han, Shu-Ping Int J Med Sci Research Paper Objectives: To explore and validate the differential expression of circRNAs in the myocardium of congenital ventricular septal defect (VSD) and to explore a new avenue of research regarding the pathological mechanisms of VSD. Methods: We detected circRNAs expression profiles in heart tissues taken from six aborted fetuses with VSD and normal group using circRNA microarray. Some differentially expressed circRNAs were studied by bioinformatics analysis. Finally, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was performed to confirm these results. Results: This study found abundant circRNAs in the myocardium taken from individuals in the normal group and the VSD group. After that, totally 6234 differentially expressed circRNAs between the normal group and the VSD group were confirmed (Fold change ≥ 2.0; p < 0.05). Then, this research carried out bioinformatics analysis and predicted the potential biological functions of circRNAs. Finally, the over-expression of hsa_circRNA_002086 and under-expression of hsa_circRNA_007878, hsa_circRNA_100709, hsa_circRNA_101965, hsa_circRNA_402565 were further validated by qRT-PCR. Conclusions: There is a significant difference in expression of the circRNA in cardiac tissue from VSD group compared to the normal group. Combined with the microarray results and previous researches, circRNAs may contribute to the occurrence of VSD by acting as miRNA sponges or by binding proteins, these possible roles for circRNAs in VSD require elucidation in additional studies. Ivyspring International Publisher 2018-05-14 /pmc/articles/PMC6001411/ /pubmed/29910675 http://dx.doi.org/10.7150/ijms.21660 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
Liu, Heng
Hu, Yin
Zhuang, Bin
Yin, Jing
Chen, Xiao-Hui
Wang, Juan
Li, Meng-Meng
Xu, Jing
Wang, Xing-Yun
Yu, Zhang-Bin
Han, Shu-Ping
Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title_full Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title_fullStr Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title_full_unstemmed Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title_short Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
title_sort differential expression of circrnas in embryonic heart tissue associated with ventricular septal defect
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001411/
https://www.ncbi.nlm.nih.gov/pubmed/29910675
http://dx.doi.org/10.7150/ijms.21660
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