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Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing
Abdominal aortic aneurysm (AAA) is a common and serious disease with a high mortality rate, but its genetic determinants have not been fully identified. In this feasibility study, we aimed to elucidate the transcriptome profile of AAA and further reveal its molecular mechanisms through the Oxford Na...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807055/ https://www.ncbi.nlm.nih.gov/pubmed/35104432 http://dx.doi.org/10.1098/rsob.210172 |
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author | Xin, Hai He, Xingqiang Li, Jun Guan, Xiaomei Liu, Xukui Wang, Yuewei Niu, Liyuan Qiu, Deqiang Wu, Xuejun Wang, Haofu |
author_facet | Xin, Hai He, Xingqiang Li, Jun Guan, Xiaomei Liu, Xukui Wang, Yuewei Niu, Liyuan Qiu, Deqiang Wu, Xuejun Wang, Haofu |
author_sort | Xin, Hai |
collection | PubMed |
description | Abdominal aortic aneurysm (AAA) is a common and serious disease with a high mortality rate, but its genetic determinants have not been fully identified. In this feasibility study, we aimed to elucidate the transcriptome profile of AAA and further reveal its molecular mechanisms through the Oxford Nanopore Technologies (ONT) MinION platform. Overall, 9574 novel transcripts and 781 genes were identified by comparing and analysing the redundant-removed transcripts of all samples with known reference genome annotations. We characterized the alternative splicing, alternative polyadenylation events and simple sequence repeat (SSR) loci information based on full-length transcriptome data, which would help us further understand the genome annotation and gene structure of AAA. Moreover, we proved that ONT methods were suitable for the identification of lncRNAs via identifying the comprehensive expression profile of lncRNAs in AAA. The results of differentially expressed transcript (DET) analysis showed that a total of 7044 transcripts were differentially expressed, of which 4278 were upregulated and 2766 were downregulated among two groups. In the KEGG analysis, 4071 annotated DETs were involved in human diseases, organismal systems and environmental information processing. These pilot findings might provide novel insights into the pathogenesis of AAA and provide new ideas for the optimization of personalized treatment of AAA, which is worthy of further study in subsequent studies. |
format | Online Article Text |
id | pubmed-8807055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88070552022-02-05 Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing Xin, Hai He, Xingqiang Li, Jun Guan, Xiaomei Liu, Xukui Wang, Yuewei Niu, Liyuan Qiu, Deqiang Wu, Xuejun Wang, Haofu Open Biol Research Abdominal aortic aneurysm (AAA) is a common and serious disease with a high mortality rate, but its genetic determinants have not been fully identified. In this feasibility study, we aimed to elucidate the transcriptome profile of AAA and further reveal its molecular mechanisms through the Oxford Nanopore Technologies (ONT) MinION platform. Overall, 9574 novel transcripts and 781 genes were identified by comparing and analysing the redundant-removed transcripts of all samples with known reference genome annotations. We characterized the alternative splicing, alternative polyadenylation events and simple sequence repeat (SSR) loci information based on full-length transcriptome data, which would help us further understand the genome annotation and gene structure of AAA. Moreover, we proved that ONT methods were suitable for the identification of lncRNAs via identifying the comprehensive expression profile of lncRNAs in AAA. The results of differentially expressed transcript (DET) analysis showed that a total of 7044 transcripts were differentially expressed, of which 4278 were upregulated and 2766 were downregulated among two groups. In the KEGG analysis, 4071 annotated DETs were involved in human diseases, organismal systems and environmental information processing. These pilot findings might provide novel insights into the pathogenesis of AAA and provide new ideas for the optimization of personalized treatment of AAA, which is worthy of further study in subsequent studies. The Royal Society 2022-02-02 /pmc/articles/PMC8807055/ /pubmed/35104432 http://dx.doi.org/10.1098/rsob.210172 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Xin, Hai He, Xingqiang Li, Jun Guan, Xiaomei Liu, Xukui Wang, Yuewei Niu, Liyuan Qiu, Deqiang Wu, Xuejun Wang, Haofu Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title | Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title_full | Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title_fullStr | Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title_full_unstemmed | Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title_short | Profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct RNA sequencing |
title_sort | profiling of the full-length transcriptome in abdominal aortic aneurysm using nanopore-based direct rna sequencing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807055/ https://www.ncbi.nlm.nih.gov/pubmed/35104432 http://dx.doi.org/10.1098/rsob.210172 |
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