• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Alternative splicing factors and cardiac disease: more than just missplicing?可变剪接因子与心脏病:仅仅是剪接错误吗?
RNA. 2025 Feb 19;31(3):300-306. doi: 10.1261/rna.080332.124.
2
Alternative Splicing in the Heart: The Therapeutic Potential of Regulating the Regulators.心脏中的可变剪接:调控调控因子的治疗潜力
Int J Mol Sci. 2024 Dec 4;25(23):13023. doi: 10.3390/ijms252313023.
3
Cardiomyocyte-Specific Long Noncoding RNA Regulates Alternative Splicing of the Triadin Gene in the Heart.心肌细胞特异性长非编码 RNA 调节心脏中三联蛋白基因的可变剪接。
Circulation. 2022 Aug 30;146(9):699-714. doi: 10.1161/CIRCULATIONAHA.121.058017. Epub 2022 Jul 18.
4
A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.RNA 结合蛋白 20 的谷氨酸丰富区的突变通过肌联蛋白的错剪接和弗兰克-斯塔尔机制受损导致扩张型心肌病。
Cardiovasc Res. 2016 Oct;112(1):452-63. doi: 10.1093/cvr/cvw192. Epub 2016 Aug 5.
5
RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing.RNA结合蛋白RBM20通过抑制剪接来协调心脏前体mRNA的加工。
J Clin Invest. 2014 Aug;124(8):3419-30. doi: 10.1172/JCI74523. Epub 2014 Jun 24.
6
Cardiac circRNAs arise mainly from constitutive exons rather than alternatively spliced exons.心脏 circRNAs 主要来自组成性外显子,而不是选择性剪接外显子。
RNA. 2018 Jun;24(6):815-827. doi: 10.1261/rna.064394.117. Epub 2018 Mar 22.
7
Splicing factors in the heart: Uncovering shared and unique targets.心脏中的剪接因子:揭示共同和独特的靶点。
J Mol Cell Cardiol. 2023 Jun;179:72-79. doi: 10.1016/j.yjmcc.2023.04.003. Epub 2023 Apr 13.
8
The Emerging Role of the RBM20 and PTBP1 Ribonucleoproteins in Heart Development and Cardiovascular Diseases.RBM20 和 PTBP1 核糖核蛋白在心脏发育和心血管疾病中的新兴作用。
Genes (Basel). 2020 Apr 8;11(4):402. doi: 10.3390/genes11040402.
9
The emerging role of alternative splicing in senescence and aging.剪接变异在衰老和老化中的新兴作用。
Aging Cell. 2017 Oct;16(5):918-933. doi: 10.1111/acel.12646. Epub 2017 Jul 13.
10
Reducing Granules Without Splicing Restoration Alleviates RBM20 Cardiomyopathy.减少无剪接恢复的颗粒可减轻RBM20心肌病。
Circ Res. 2025 May 9;136(10):1134-1146. doi: 10.1161/CIRCRESAHA.124.324781. Epub 2025 Apr 17.

引用本文的文献

1
Biomolecular condensates in plant immunity.植物免疫中的生物分子凝聚物
Cell Host Microbe. 2025 Aug 13;33(8):1276-1290. doi: 10.1016/j.chom.2025.06.014.

本文引用的文献

1
Therapeutic potential of alternative splicing in cardiovascular diseases.替代剪接在心血管疾病中的治疗潜力。
EBioMedicine. 2024 Mar;101:104995. doi: 10.1016/j.ebiom.2024.104995. Epub 2024 Feb 12.
2
Mechanisms of RBM20 Cardiomyopathy: Insights From Model Systems.RBM20 心肌病的发病机制:模型系统的新见解。
Circ Genom Precis Med. 2024 Feb;17(1):e004355. doi: 10.1161/CIRCGEN.123.004355. Epub 2024 Jan 30.
3
Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.Celf4 控制着哺乳动物胚胎大脑皮质发育过程中的突触发育所必需的 mRNA 翻译。
Nat Commun. 2023 Sep 27;14(1):6025. doi: 10.1038/s41467-023-41730-8.
4
Coordination of alternative splicing and alternative polyadenylation revealed by targeted long read sequencing.通过靶向长读测序揭示的可变剪接和可变多聚腺苷酸化的协调作用。
Nat Commun. 2023 Sep 7;14(1):5506. doi: 10.1038/s41467-023-41207-8.
5
Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3.致病性 RBM20 变异体在扩张型心肌病中的定位错误是由于与 Transportin-3 相互作用丧失所致。
Nat Commun. 2023 Jul 18;14(1):4312. doi: 10.1038/s41467-023-39965-6.
6
Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy.横纹肌特异性碱基编辑可纠正导致扩张型心肌病的突变。
Nat Commun. 2023 Jun 22;14(1):3714. doi: 10.1038/s41467-023-39352-1.
7
Biallelic variants in RBM42 cause a multisystem disorder with neurological, facial, cardiac, and musculoskeletal involvement.RBM42 中的双等位基因变异导致一种多系统疾病,涉及神经、面部、心脏和肌肉骨骼。
Protein Cell. 2024 Jan 3;15(1):52-68. doi: 10.1093/procel/pwad034.
8
Disruption of the nuclear localization signal in RBM20 is causative in dilated cardiomyopathy.RBM20 核定位信号的破坏可导致扩张型心肌病。
JCI Insight. 2023 Jul 10;8(13):e170001. doi: 10.1172/jci.insight.170001.
9
Splicing factors in the heart: Uncovering shared and unique targets.心脏中的剪接因子:揭示共同和独特的靶点。
J Mol Cell Cardiol. 2023 Jun;179:72-79. doi: 10.1016/j.yjmcc.2023.04.003. Epub 2023 Apr 13.
10
Precise genomic editing of pathogenic mutations in rescues dilated cardiomyopathy.精确的基因组编辑可纠正致病性突变,从而挽救扩张型心肌病。
Sci Transl Med. 2022 Nov 23;14(672):eade1633. doi: 10.1126/scitranslmed.ade1633.

可变剪接因子与心脏病:仅仅是剪接错误吗?

Alternative splicing factors and cardiac disease: more than just missplicing?

作者信息

Gregorich Zachery R, Guo Wei

机构信息

Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA

出版信息

RNA. 2025 Feb 19;31(3):300-306. doi: 10.1261/rna.080332.124.

DOI:10.1261/rna.080332.124
PMID:39773891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11874993/
Abstract

Alternative splicing (AS) is the process wherein the exons from a single gene are joined in different combinations to produce nonidentical, albeit related, RNA transcripts. This process is important for the development and physiological function of many organs and is particularly important in the heart. Notably, AS has been implicated in cardiac disease and failure, and a growing number of genetic variants in AS factors have been identified in association with cardiac malformation and/or disease. With the field poised to interrogate how these variants affect cardiac development and disease, an understandable point of emphasis will undoubtedly be on downstream target gene missplicing. In this Perspective article, we would like to encourage consideration not only of the potential for novel disease mechanisms, but also for contributions from disruption of the ever-expanding list of nonsplicing functions ascribed to many AS factors. We discuss the emergence of a novel cardiac disease mechanism based on pathogenic RNA granules and speculate on the generality of such a mechanism among localization-disrupting AS factor genetic variants. We also highlight emerging nonsplicing functions attributed to several AS factors with cardiac disease-associated genetic variants in the hopes of pointing to avenues for exploration of mechanisms that may contribute to disease alongside target gene missplicing.

摘要

可变剪接(AS)是指来自单个基因的外显子以不同组合方式拼接在一起,从而产生虽相关但不同的RNA转录本的过程。这一过程对许多器官的发育和生理功能至关重要,在心脏中尤为重要。值得注意的是,可变剪接与心脏疾病和心脏衰竭有关,并且已经鉴定出越来越多与心脏畸形和/或疾病相关的可变剪接因子的遗传变异。随着该领域准备探究这些变异如何影响心脏发育和疾病,一个可以理解的重点无疑将放在下游靶基因的错误剪接上。在这篇观点文章中,我们不仅鼓励考虑新疾病机制的可能性,还要考虑许多可变剪接因子所具有的不断扩展的非剪接功能被破坏所带来的影响。我们讨论了一种基于致病性RNA颗粒的新型心脏疾病机制,并推测这种机制在破坏定位的可变剪接因子遗传变异中的普遍性。我们还强调了归因于几种与心脏疾病相关的遗传变异的可变剪接因子的新出现的非剪接功能,希望能指出除了靶基因错误剪接之外,可能导致疾病的机制的探索途径。