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RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract
BACKGROUND: Age-related cataract (ARC) is the main cause of blindness in older individuals but its specific pathogenic mechanism is unclear. This study aimed to identify differentially expressed genes (DEGs) associated with ARC and to improve our understanding of the disease mechanism. METHODS: Ante...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995707/ https://www.ncbi.nlm.nih.gov/pubmed/33771123 http://dx.doi.org/10.1186/s12886-021-01915-5 |
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author | Wang, Zhongying Su, Dongmei Liu, Shanhe Zheng, Guiqian Zhang, Gaobo Cui, Tingsong Ma, Xu Sun, Zhaoyi Hu, Shanshan |
author_facet | Wang, Zhongying Su, Dongmei Liu, Shanhe Zheng, Guiqian Zhang, Gaobo Cui, Tingsong Ma, Xu Sun, Zhaoyi Hu, Shanshan |
author_sort | Wang, Zhongying |
collection | PubMed |
description | BACKGROUND: Age-related cataract (ARC) is the main cause of blindness in older individuals but its specific pathogenic mechanism is unclear. This study aimed to identify differentially expressed genes (DEGs) associated with ARC and to improve our understanding of the disease mechanism. METHODS: Anterior capsule samples of the human lens were collected from ARC patients and healthy controls and used for RNA sequencing to detect DEGs. Identified DEGs underwent bioinformatics analyses, including Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. Subsequently, reverse transcription quantitative RT-qPCR was used to validate the different expression levels of selected genes. RESULTS: A total of 698 up-regulated DEGs and 414 down-regulated DEGs were identified in ARC patients compared with controls by transcriptome analysis. Through GO and KEGG bioinformatics analysis, the functions of significantly DEGs and their possible molecular mechanisms were determined. Sequencing results were verified by RT-qPCR as being accurate and reliable. CONCLUSIONS: This study identified several genes associated with ARC, which improves our knowledge of the disease mechanism. |
format | Online Article Text |
id | pubmed-7995707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79957072021-03-26 RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract Wang, Zhongying Su, Dongmei Liu, Shanhe Zheng, Guiqian Zhang, Gaobo Cui, Tingsong Ma, Xu Sun, Zhaoyi Hu, Shanshan BMC Ophthalmol Research Article BACKGROUND: Age-related cataract (ARC) is the main cause of blindness in older individuals but its specific pathogenic mechanism is unclear. This study aimed to identify differentially expressed genes (DEGs) associated with ARC and to improve our understanding of the disease mechanism. METHODS: Anterior capsule samples of the human lens were collected from ARC patients and healthy controls and used for RNA sequencing to detect DEGs. Identified DEGs underwent bioinformatics analyses, including Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. Subsequently, reverse transcription quantitative RT-qPCR was used to validate the different expression levels of selected genes. RESULTS: A total of 698 up-regulated DEGs and 414 down-regulated DEGs were identified in ARC patients compared with controls by transcriptome analysis. Through GO and KEGG bioinformatics analysis, the functions of significantly DEGs and their possible molecular mechanisms were determined. Sequencing results were verified by RT-qPCR as being accurate and reliable. CONCLUSIONS: This study identified several genes associated with ARC, which improves our knowledge of the disease mechanism. BioMed Central 2021-03-26 /pmc/articles/PMC7995707/ /pubmed/33771123 http://dx.doi.org/10.1186/s12886-021-01915-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Wang, Zhongying Su, Dongmei Liu, Shanhe Zheng, Guiqian Zhang, Gaobo Cui, Tingsong Ma, Xu Sun, Zhaoyi Hu, Shanshan RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title | RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title_full | RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title_fullStr | RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title_full_unstemmed | RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title_short | RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
title_sort | rna sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995707/ https://www.ncbi.nlm.nih.gov/pubmed/33771123 http://dx.doi.org/10.1186/s12886-021-01915-5 |
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