• 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

包含脊髓性肌萎缩症基因四个早期外显子的环状 RNA 的转录组和蛋白质组的影响。

Transcriptome- and proteome-wide effects of a circular RNA encompassing four early exons of the spinal muscular atrophy genes.

机构信息

Department of Biomedical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA, 50011, USA.

出版信息

Sci Rep. 2024 May 7;14(1):10442. doi: 10.1038/s41598-024-60593-7.

DOI:10.1038/s41598-024-60593-7
PMID:38714739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11076517/
Abstract

Spinal muscular atrophy (SMA) genes, SMN1 and SMN2 (hereinafter referred to as SMN1/2), produce multiple circular RNAs (circRNAs), including C2A-2B-3-4 that encompasses early exons 2A, 2B, 3 and 4. C2A-2B-3-4 is a universally and abundantly expressed circRNA of SMN1/2. Here we report the transcriptome- and proteome-wide effects of overexpression of C2A-2B-3-4 in inducible HEK293 cells. Our RNA-Seq analysis revealed altered expression of ~ 15% genes (4172 genes) by C2A-2B-3-4. About half of the affected genes by C2A-2B-3-4 remained unaffected by L2A-2B-3-4, a linear transcript encompassing exons 2A, 2B, 3 and 4 of SMN1/2. These findings underscore the unique role of the structural context of C2A-2B-3-4 in gene regulation. A surprisingly high number of upregulated genes by C2A-2B-3-4 were located on chromosomes 4 and 7, whereas many of the downregulated genes were located on chromosomes 10 and X. Supporting a cross-regulation of SMN1/2 transcripts, C2A-2B-3-4 and L2A-2B-3-4 upregulated and downregulated SMN1/2 mRNAs, respectively. Proteome analysis revealed 61 upregulated and 57 downregulated proteins by C2A-2B-3-4 with very limited overlap with those affected by L2A-2B-3-4. Independent validations confirmed the effect of C2A-2B-3-4 on expression of genes associated with chromatin remodeling, transcription, spliceosome function, ribosome biogenesis, lipid metabolism, cytoskeletal formation, cell proliferation and neuromuscular junction formation. Our findings reveal a broad role of C2A-2B-3-4, and expands our understanding of functions of SMN1/2 genes.

摘要

脊髓性肌萎缩症(SMA)基因 SMN1 和 SMN2(以下简称 SMN1/2)产生多种环状 RNA(circRNA),包括包含早期外显子 2A、2B、3 和 4 的 C2A-2B-3-4。C2A-2B-3-4 是 SMN1/2 普遍且丰富表达的 circRNA。在这里,我们报告了在诱导型 HEK293 细胞中过表达 C2A-2B-3-4 对转录组和蛋白质组的广泛影响。我们的 RNA-Seq 分析显示,C2A-2B-3-4 改变了约 15%的基因(4172 个基因)的表达。C2A-2B-3-4 影响的大约一半基因不受 L2A-2B-3-4 的影响,L2A-2B-3-4 是包含 SMN1/2 的外显子 2A、2B、3 和 4 的线性转录本。这些发现强调了 C2A-2B-3-4 在基因调控中的结构环境的独特作用。C2A-2B-3-4 上调的基因数量惊人地高,位于染色体 4 和 7 上,而许多下调的基因位于染色体 10 和 X 上。支持 SMN1/2 转录物的交叉调节,C2A-2B-3-4 和 L2A-2B-3-4 分别上调和下调 SMN1/2 mRNA。蛋白质组分析显示,C2A-2B-3-4 上调了 61 个蛋白,下调了 57 个蛋白,与 L2A-2B-3-4 影响的蛋白很少重叠。独立验证证实了 C2A-2B-3-4 对与染色质重塑、转录、剪接体功能、核糖体生物发生、脂质代谢、细胞骨架形成、细胞增殖和神经肌肉接头形成相关基因表达的影响。我们的研究结果揭示了 C2A-2B-3-4 的广泛作用,并扩展了我们对 SMN1/2 基因功能的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/385a7cd06338/41598_2024_60593_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/eda12eb23f23/41598_2024_60593_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/d0d0a9eb1f91/41598_2024_60593_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/6329fba42867/41598_2024_60593_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/dc5dff25b0bf/41598_2024_60593_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/1de16e3e84f0/41598_2024_60593_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/9b6892de469b/41598_2024_60593_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/385a7cd06338/41598_2024_60593_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/eda12eb23f23/41598_2024_60593_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/d0d0a9eb1f91/41598_2024_60593_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/6329fba42867/41598_2024_60593_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/dc5dff25b0bf/41598_2024_60593_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/1de16e3e84f0/41598_2024_60593_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/9b6892de469b/41598_2024_60593_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0882/11076517/385a7cd06338/41598_2024_60593_Fig7_HTML.jpg

相似文献

1
Transcriptome- and proteome-wide effects of a circular RNA encompassing four early exons of the spinal muscular atrophy genes.包含脊髓性肌萎缩症基因四个早期外显子的环状 RNA 的转录组和蛋白质组的影响。
Sci Rep. 2024 May 7;14(1):10442. doi: 10.1038/s41598-024-60593-7.
2
Transcriptome- and proteome-wide effects of a circular RNA encompassing four early exons of the spinal muscular atrophy genes.包含脊髓性肌萎缩症基因四个早期外显子的环状RNA对转录组和蛋白质组的广泛影响。
Res Sq. 2024 Feb 28:rs.3.rs-3818622. doi: 10.21203/rs.3.rs-3818622/v1.
3
Internal Introns Promote Backsplicing to Generate Circular RNAs from Spinal Muscular Atrophy Gene.内含子促进反式剪接产生来自脊髓性肌萎缩症基因的环状 RNA
Genes (Basel). 2022 Jun 25;13(7):1145. doi: 10.3390/genes13071145.
4
Revealing diverse alternative splicing variants of the highly homologous SMN1 and SMN2 genes by targeted long-read sequencing.通过靶向长读测序揭示高度同源的 SMN1 和 SMN2 基因的多样化可变剪接变体。
Mol Genet Genomics. 2022 Jul;297(4):1039-1048. doi: 10.1007/s00438-022-01874-6. Epub 2022 May 25.
5
Characteristics of circular RNAs generated by human Survival Motor Neuron genes.人存活运动神经元基因产生的环状 RNA 的特征。
Cell Signal. 2020 Sep;73:109696. doi: 10.1016/j.cellsig.2020.109696. Epub 2020 Jun 15.
6
Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes.脊髓性肌萎缩症基因的剪接调控机制。
Adv Neurobiol. 2018;20:31-61. doi: 10.1007/978-3-319-89689-2_2.
7
Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene.氧化应激引发脊髓性肌萎缩症基因多个外显子在全身范围内的跳跃。
PLoS One. 2016 Apr 25;11(4):e0154390. doi: 10.1371/journal.pone.0154390. eCollection 2016.
8
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene.脊髓性肌萎缩症患者的混合 SMN 基因的临床表型。
Brain Dev. 2021 Feb;43(2):294-302. doi: 10.1016/j.braindev.2020.09.005. Epub 2020 Oct 6.
9
Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.脊髓性肌萎缩症基因SMN1和SMN2的内含子保留转录本。
Brain Dev. 2018 Sep;40(8):670-677. doi: 10.1016/j.braindev.2018.03.001. Epub 2018 Mar 23.
10
Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis.神经钙蛋白δ抑制通过恢复受损的内吞作用,对人类及跨物种的脊髓性肌萎缩起到保护作用。
Am J Hum Genet. 2017 Feb 2;100(2):297-315. doi: 10.1016/j.ajhg.2017.01.005. Epub 2017 Jan 26.

引用本文的文献

1
Translation of circular RNAs.环状RNA的翻译。
Nucleic Acids Res. 2025 Jan 7;53(1). doi: 10.1093/nar/gkae1167.

本文引用的文献

1
A super minigene with a short promoter and truncated introns recapitulates essential features of transcription and splicing regulation of the SMN1 and SMN2 genes.一个带有短启动子和截短内含子的超级微型基因概括了SMN1和SMN2基因转录和剪接调控的基本特征。
Nucleic Acids Res. 2024 Apr 24;52(7):3547-3571. doi: 10.1093/nar/gkad1259.
2
Roles of circRNAs in regulating the tumor microenvironment.环状 RNA 在调节肿瘤微环境中的作用。
Med Oncol. 2023 Oct 11;40(11):329. doi: 10.1007/s12032-023-02194-4.
3
Alzheimer's disease pathogenetic progression is associated with changes in regulated retained introns and editing of circular RNAs.
阿尔茨海默病的发病机制进展与可变保留内含子的变化以及环状RNA的编辑有关。
Front Mol Neurosci. 2023 May 5;16:1141079. doi: 10.3389/fnmol.2023.1141079. eCollection 2023.
4
Understanding the roles and regulation patterns of circRNA on its host gene in tumorigenesis and tumor progression.解析 circRNA 对其宿主基因在肿瘤发生和肿瘤进展中的作用和调控模式。
J Exp Clin Cancer Res. 2023 Apr 15;42(1):86. doi: 10.1186/s13046-023-02657-6.
5
The RNA-Binding Protein SMN as a Novel Player in Laryngeal Squamous Cell Carcinoma.RNA 结合蛋白 SMN 作为喉鳞状细胞癌的新角色。
Int J Mol Sci. 2023 Jan 16;24(2):1794. doi: 10.3390/ijms24021794.
6
The Depletion of NAMPT Disturbs Mitochondrial Homeostasis and Causes Neuronal Degeneration in Mouse Hippocampus.NAMPT 的耗竭扰乱了线粒体的动态平衡,并导致小鼠海马神经元变性。
Mol Neurobiol. 2023 Mar;60(3):1267-1280. doi: 10.1007/s12035-022-03142-5. Epub 2022 Nov 28.
7
Internal Introns Promote Backsplicing to Generate Circular RNAs from Spinal Muscular Atrophy Gene.内含子促进反式剪接产生来自脊髓性肌萎缩症基因的环状 RNA
Genes (Basel). 2022 Jun 25;13(7):1145. doi: 10.3390/genes13071145.
8
Structural Mechanism of TAF-Iβ Chaperone Function on Linker Histone H1.10.TAF-Iβ 对连接组蛋白 H1.10 的伴侣功能的结构机制。
J Mol Biol. 2022 Oct 15;434(19):167755. doi: 10.1016/j.jmb.2022.167755. Epub 2022 Jul 21.
9
R-loop Mediated DNA Damage and Impaired DNA Repair in Spinal Muscular Atrophy.R环介导的脊髓性肌萎缩症中的DNA损伤与DNA修复受损
Front Cell Neurosci. 2022 Jun 16;16:826608. doi: 10.3389/fncel.2022.826608. eCollection 2022.
10
An exercise-inducible metabolite that suppresses feeding and obesity.一种可诱导运动的代谢物,可抑制进食和肥胖。
Nature. 2022 Jun;606(7915):785-790. doi: 10.1038/s41586-022-04828-5. Epub 2022 Jun 15.