The alternative splicing landscape of infarcted mouse heart identifies isoform level therapeutic targets.

IF 5.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Scientific Data Pub Date : 2024-10-18 DOI:10.1038/s41597-024-03998-3
Binbin Xia, Jianghua Shen, Hao Zhang, Siqi Chen, Xuan Zhang, Moshi Song, Jun Wang
{"title":"The alternative splicing landscape of infarcted mouse heart identifies isoform level therapeutic targets.","authors":"Binbin Xia, Jianghua Shen, Hao Zhang, Siqi Chen, Xuan Zhang, Moshi Song, Jun Wang","doi":"10.1038/s41597-024-03998-3","DOIUrl":null,"url":null,"abstract":"<p><p>Alternative splicing is an important process that contributes to highly diverse transcripts and protein products, which can affect the development of disease in various organisms. Cardiovascular disease (CVD) represents one of the greatest global threats to humans, particularly acute myocardial infarction (MI) and subsequent ischemic reperfusion (IR) injury, which involve complex transcriptomic changes in heart tissues associated with metabolic reshaping and immunological response. In this study, we used a newly developed ONT full-length transcriptomic approach and performed transcript-resolved differential expression profiling in murine models of MI and IR. We built an analytical pipeline to reliably identify and quantify alternative splicing products (isoforms), expanding on the currently available catalog of isoforms described in mice. The updated alternative splicing landscape included transcripts, genes, and pathways that were differentially regulated during IR and MI. Our study establishes a pipeline to profile highly diverse isoforms using state-of-the-art long-read sequencing, builds a landscape of alternative splicing in the mouse heart during MI and IR.</p>","PeriodicalId":21597,"journal":{"name":"Scientific Data","volume":"11 1","pages":"1154"},"PeriodicalIF":5.8000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11489681/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scientific Data","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41597-024-03998-3","RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Alternative splicing is an important process that contributes to highly diverse transcripts and protein products, which can affect the development of disease in various organisms. Cardiovascular disease (CVD) represents one of the greatest global threats to humans, particularly acute myocardial infarction (MI) and subsequent ischemic reperfusion (IR) injury, which involve complex transcriptomic changes in heart tissues associated with metabolic reshaping and immunological response. In this study, we used a newly developed ONT full-length transcriptomic approach and performed transcript-resolved differential expression profiling in murine models of MI and IR. We built an analytical pipeline to reliably identify and quantify alternative splicing products (isoforms), expanding on the currently available catalog of isoforms described in mice. The updated alternative splicing landscape included transcripts, genes, and pathways that were differentially regulated during IR and MI. Our study establishes a pipeline to profile highly diverse isoforms using state-of-the-art long-read sequencing, builds a landscape of alternative splicing in the mouse heart during MI and IR.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
梗死小鼠心脏的替代剪接图谱确定了同工酶水平的治疗目标。
替代剪接是一个重要的过程,可产生高度多样化的转录本和蛋白质产物,从而影响各种生物体的疾病发展。心血管疾病(CVD)是人类面临的最大全球性威胁之一,尤其是急性心肌梗塞(MI)和随后的缺血再灌注(IR)损伤,涉及心脏组织中与代谢重塑和免疫反应相关的复杂转录组变化。在这项研究中,我们使用了一种新开发的 ONT 全长转录组方法,并在 MI 和 IR 的小鼠模型中进行了转录本分辨差异表达谱分析。我们建立了一个分析管道来可靠地识别和量化替代剪接产物(同工酶),扩展了目前可用的小鼠同工酶目录。更新后的替代剪接图谱包括在IR和MI期间受到不同调控的转录本、基因和通路。我们的研究利用最先进的长线程测序技术建立了一个分析高度多样化异构体的管道,构建了小鼠心脏在心肌梗死和心肌梗死期间的替代剪接图谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Scientific Data
Scientific Data Social Sciences-Education
CiteScore
11.20
自引率
4.10%
发文量
689
审稿时长
16 weeks
期刊介绍: Scientific Data is an open-access journal focused on data, publishing descriptions of research datasets and articles on data sharing across natural sciences, medicine, engineering, and social sciences. Its goal is to enhance the sharing and reuse of scientific data, encourage broader data sharing, and acknowledge those who share their data. The journal primarily publishes Data Descriptors, which offer detailed descriptions of research datasets, including data collection methods and technical analyses validating data quality. These descriptors aim to facilitate data reuse rather than testing hypotheses or presenting new interpretations, methods, or in-depth analyses.
期刊最新文献
A chromosome-level genome assembly of the heteronomous hyperparasitoid wasp Encarsia sophia. A geospatial dataset of lichen key attributes in the Earth's three poles. An fMRI dataset in response to large-scale short natural dynamic facial expression videos. Chromosome-level genome assembly of the mud carp (Cirrhinus molitorella) using PacBio HiFi and Hi-C sequencing. An annual land cover dataset for the Baltic Sea Region with crop types and peat bogs at 30 m from 2000 to 2022.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1