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Comprehensive analysis of circRNA expression profiles in humans by RAISE
Circular RNAs (circRNAs) are pervasively expressed circles of non-coding RNAs. Even though many circRNAs have been reported in humans, their expression patterns and functions remain poorly understood. In this study, we employed a pipeline named RAISE to detect circRNAs in RNA-seq data. RAISE can ful...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673025/ https://www.ncbi.nlm.nih.gov/pubmed/29039477 http://dx.doi.org/10.3892/ijo.2017.4162 |
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author | Li, Lin Zheng, Yong-Chang Kayani, Masood Ur Rehman Xu, Wen Wang, Guan-Qun Sun, Pei Ao, Ning Zhang, Li-Na Gu, Zhao-Qi Wu, Liang-Cai Zhao, Hai-Tao |
author_facet | Li, Lin Zheng, Yong-Chang Kayani, Masood Ur Rehman Xu, Wen Wang, Guan-Qun Sun, Pei Ao, Ning Zhang, Li-Na Gu, Zhao-Qi Wu, Liang-Cai Zhao, Hai-Tao |
author_sort | Li, Lin |
collection | PubMed |
description | Circular RNAs (circRNAs) are pervasively expressed circles of non-coding RNAs. Even though many circRNAs have been reported in humans, their expression patterns and functions remain poorly understood. In this study, we employed a pipeline named RAISE to detect circRNAs in RNA-seq data. RAISE can fully characterize circRNA structure and abundance. We evaluated inter-individual variations in circRNA expression in humans by applying this pipeline to numerous non-poly(A)-selected RNA-seq data. We identified 59,128 circRNA candidates in 61 human liver samples, with almost no overlap in the circRNA of the recruited samples. Approximately 89% of the circRNAs were detected in one or two samples. In comparison, 10% of the linear mRNAs and non-coding RNAs were detected in each sample. We estimated the variation in other tissues, especially the circRNA high-abundance tissues, in advance. Only 0.5% of the 50,631 brain circRNA candidates were shared among the 30 recruited brain samples, which is similar to the proportion in liver. Moreover, we found inter- and intra-individual diversity in circRNAs expression in the granulocyte RNA-seq data from seven individuals sampled 3 times at one-month intervals. Our findings suggest that careful consideration of inter-individual diversity is required when extensively identifying human circRNAs or proposing their use as potential biomarkers and therapeutic targets in disease. |
format | Online Article Text |
id | pubmed-5673025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-56730252017-11-16 Comprehensive analysis of circRNA expression profiles in humans by RAISE Li, Lin Zheng, Yong-Chang Kayani, Masood Ur Rehman Xu, Wen Wang, Guan-Qun Sun, Pei Ao, Ning Zhang, Li-Na Gu, Zhao-Qi Wu, Liang-Cai Zhao, Hai-Tao Int J Oncol Articles Circular RNAs (circRNAs) are pervasively expressed circles of non-coding RNAs. Even though many circRNAs have been reported in humans, their expression patterns and functions remain poorly understood. In this study, we employed a pipeline named RAISE to detect circRNAs in RNA-seq data. RAISE can fully characterize circRNA structure and abundance. We evaluated inter-individual variations in circRNA expression in humans by applying this pipeline to numerous non-poly(A)-selected RNA-seq data. We identified 59,128 circRNA candidates in 61 human liver samples, with almost no overlap in the circRNA of the recruited samples. Approximately 89% of the circRNAs were detected in one or two samples. In comparison, 10% of the linear mRNAs and non-coding RNAs were detected in each sample. We estimated the variation in other tissues, especially the circRNA high-abundance tissues, in advance. Only 0.5% of the 50,631 brain circRNA candidates were shared among the 30 recruited brain samples, which is similar to the proportion in liver. Moreover, we found inter- and intra-individual diversity in circRNAs expression in the granulocyte RNA-seq data from seven individuals sampled 3 times at one-month intervals. Our findings suggest that careful consideration of inter-individual diversity is required when extensively identifying human circRNAs or proposing their use as potential biomarkers and therapeutic targets in disease. D.A. Spandidos 2017-10-16 /pmc/articles/PMC5673025/ /pubmed/29039477 http://dx.doi.org/10.3892/ijo.2017.4162 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Li, Lin Zheng, Yong-Chang Kayani, Masood Ur Rehman Xu, Wen Wang, Guan-Qun Sun, Pei Ao, Ning Zhang, Li-Na Gu, Zhao-Qi Wu, Liang-Cai Zhao, Hai-Tao Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title | Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title_full | Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title_fullStr | Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title_full_unstemmed | Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title_short | Comprehensive analysis of circRNA expression profiles in humans by RAISE |
title_sort | comprehensive analysis of circrna expression profiles in humans by raise |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673025/ https://www.ncbi.nlm.nih.gov/pubmed/29039477 http://dx.doi.org/10.3892/ijo.2017.4162 |
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