Department of Vascular Surgery, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250021, People's Republic of China.
Department of Cardiology, Xijing Hospital, Fourth Military Medical University, 169 West Changle Road, Xi'an 710032, People's Republic of China.
Open Biol. 2022 Feb;12(2):210172. doi: 10.1098/rsob.210172. Epub 2022 Feb 2.
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.
腹主动脉瘤(AAA)是一种常见且严重的疾病,死亡率较高,但其遗传决定因素尚未完全确定。在这项可行性研究中,我们旨在通过牛津纳米孔技术(ONT)MinION 平台阐明 AAA 的转录组图谱,并进一步揭示其分子机制。总体而言,通过比较和分析所有样本中与已知参考基因组注释重复的转录本,我们确定了 9574 个新的转录本和 781 个基因。我们基于全长转录组数据对可变剪接、可变多聚腺苷酸化事件和简单重复序列(SSR)位点信息进行了特征描述,这将有助于我们进一步了解 AAA 的基因组注释和基因结构。此外,我们通过鉴定 AAA 中 lncRNA 的全面表达谱,证明了 ONT 方法适用于 lncRNA 的鉴定。差异表达转录本(DET)分析的结果表明,两组间共有 7044 个转录本存在差异表达,其中 4278 个上调,2766 个下调。KEGG 分析表明,4071 个注释 DETs 参与了人类疾病、机体系统和环境信息处理。这些初步研究结果可能为 AAA 的发病机制提供新的见解,并为优化 AAA 的个性化治疗提供新的思路,这值得在后续研究中进一步研究。