• 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

FUS突变小鼠中低读取深度QuantSeq 3'测序与全RNA测序的比较

A Comparison of Low Read Depth QuantSeq 3' Sequencing to Total RNA-Seq in FUS Mutant Mice.

作者信息

Jarvis Seth, Birsa Nicol, Secrier Maria, Fratta Pietro, Plagnol Vincent

机构信息

UCL Queen Square Institute of Neurology, London, United Kingdom.

UCL Genetics Institute, London, United Kingdom.

出版信息

Front Genet. 2020 Nov 19;11:562445. doi: 10.3389/fgene.2020.562445. eCollection 2020.

DOI:10.3389/fgene.2020.562445
PMID:33329699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7717943/
Abstract

Transcriptomics is a developing field with new methods of analysis being produced which may hold advantages in price, accuracy, or information output. QuantSeq is a form of 3' sequencing produced by Lexogen which aims to obtain similar gene-expression information to RNA-seq with significantly fewer reads, and therefore at a lower cost. QuantSeq is also able to provide information on differential polyadenylation. We applied both QuantSeq at low read depth and total RNA-seq to the same two sets of mouse spinal cord RNAs, each comprised by four controls and four mutants related to the neurodegenerative disease amyotrophic lateral sclerosis. We found substantial differences in which genes were found to be significantly differentially expressed by the two methods. Some of this difference likely due to the difference in number of reads between our QuantSeq and RNA-seq data. Other sources of difference can be explained by the differences in the way the two methods handle genes with different primary transcript lengths and how likely each method is to find a gene to be differentially expressed at different levels of overall gene expression. This work highlights how different methods aiming to assess expression difference can lead to different results.

摘要

转录组学是一个不断发展的领域,新的分析方法不断涌现,这些方法可能在价格、准确性或信息输出方面具有优势。QuantSeq是Lexogen公司开发的一种3'测序形式,旨在用明显更少的读数获得与RNA测序相似的基因表达信息,从而降低成本。QuantSeq还能够提供差异多聚腺苷酸化的信息。我们将低读数深度的QuantSeq和全RNA测序应用于两组相同的小鼠脊髓RNA,每组由四个与神经退行性疾病肌萎缩侧索硬化相关的对照和四个突变体组成。我们发现,两种方法在哪些基因被显著差异表达方面存在实质性差异。这种差异部分可能是由于我们的QuantSeq和RNA测序数据之间读数数量的差异。其他差异来源可以通过两种方法处理具有不同初级转录本长度的基因的方式差异,以及每种方法在不同总体基因表达水平下发现基因差异表达的可能性差异来解释。这项工作突出了旨在评估表达差异的不同方法如何导致不同的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4718/7717943/60112a0e8165/fgene-11-562445-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4718/7717943/1b55d1fd640a/fgene-11-562445-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4718/7717943/60112a0e8165/fgene-11-562445-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4718/7717943/1b55d1fd640a/fgene-11-562445-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4718/7717943/60112a0e8165/fgene-11-562445-g002.jpg

相似文献

1
A Comparison of Low Read Depth QuantSeq 3' Sequencing to Total RNA-Seq in FUS Mutant Mice.FUS突变小鼠中低读取深度QuantSeq 3'测序与全RNA测序的比较
Front Genet. 2020 Nov 19;11:562445. doi: 10.3389/fgene.2020.562445. eCollection 2020.
2
A comparison between whole transcript and 3' RNA sequencing methods using Kapa and Lexogen library preparation methods.使用 Kapa 和 Lexogen 文库制备方法的全转录组和 3' RNA 测序方法比较。
BMC Genomics. 2019 Jan 7;20(1):9. doi: 10.1186/s12864-018-5393-3.
3
Deploying new generation sequencing for the study of flesh color depletion in Atlantic Salmon (Salmo salar).应用新一代测序技术研究大西洋鲑鱼肉色减退。
BMC Genomics. 2021 Jul 17;22(1):545. doi: 10.1186/s12864-021-07884-9.
4
Optimizing Cost-Effective gene expression phenotyping approaches in cattle using 3' mRNA sequencing.利用3' mRNA测序优化牛的具有成本效益的基因表达表型分析方法。
BMC Genomics. 2025 Apr 16;26(1):379. doi: 10.1186/s12864-025-11571-4.
5
Application of the 3' mRNA-Seq using unique molecular identifiers in highly degraded RNA derived from formalin-fixed, paraffin-embedded tissue.使用独特分子标识符的3' mRNA测序在源自福尔马林固定石蜡包埋组织的高度降解RNA中的应用
BMC Genomics. 2021 Oct 24;22(1):759. doi: 10.1186/s12864-021-08068-1.
6
QuantSeq. 3' Sequencing combined with Salmon provides a fast, reliable approach for high throughput RNA expression analysis.QuantSeq 3' 测序与 Salmon 联合使用,为高通量 RNA 表达分析提供了一种快速、可靠的方法。
Sci Rep. 2019 Dec 11;9(1):18895. doi: 10.1038/s41598-019-55434-x.
7
Influence of RNA-Seq library construction, sampling methods, and tissue harvesting time on gene expression estimation.RNA测序文库构建、采样方法及组织采集时间对基因表达估计的影响。
Mol Ecol Resour. 2023 May;23(4):803-817. doi: 10.1111/1755-0998.13757. Epub 2023 Feb 23.
8
Accurate Quantification of Overlapping Herpesvirus Transcripts from RNA Sequencing Data.从 RNA 测序数据中准确量化重叠的疱疹病毒转录本。
J Virol. 2022 Jan 26;96(2):e0163521. doi: 10.1128/JVI.01635-21. Epub 2021 Oct 27.
9
The effects of a globin blocker on the resolution of 3'mRNA sequencing data in porcine blood.球蛋白阻断剂对猪血液 3'mRNA 测序数据解析的影响。
BMC Genomics. 2019 Oct 15;20(1):741. doi: 10.1186/s12864-019-6122-2.
10
MustSeq, an alternative approach for multiplexible strand-specific 3' end sequencing of mRNA transcriptome confers high efficiency and practicality.MustSeq 是一种用于对 mRNA 转录组进行多重、有向 3' 端测序的替代方法,具有高效、实用的特点。
RNA Biol. 2021 Oct 15;18(sup1):232-243. doi: 10.1080/15476286.2021.1974208. Epub 2021 Sep 29.

引用本文的文献

1
Optimizing Cost-Effective gene expression phenotyping approaches in cattle using 3' mRNA sequencing.利用3' mRNA测序优化牛的具有成本效益的基因表达表型分析方法。
BMC Genomics. 2025 Apr 16;26(1):379. doi: 10.1186/s12864-025-11571-4.
2
Varying conjunctival immune response adaptations of house finch populations to a rapidly evolving bacterial pathogen.雀形目鸟类对快速进化的细菌病原体的结膜免疫反应适应性存在差异。
Front Immunol. 2024 Feb 2;15:1250818. doi: 10.3389/fimmu.2024.1250818. eCollection 2024.
3
3' RNA-seq is superior to standard RNA-seq in cases of sparse data but inferior at identifying toxicity pathways in a model organism.

本文引用的文献

1
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention.FUS 肌萎缩侧索硬化症相关突变通过内含子保留损害 FUS 自身调控和剪接因子网络。
Nucleic Acids Res. 2020 Jul 9;48(12):6889-6905. doi: 10.1093/nar/gkaa410.
2
Abnormal Upregulation of GPR17 Receptor Contributes to Oligodendrocyte Dysfunction in SOD1 G93A Mice.GPR17 受体异常上调导致 SOD1 G93A 小鼠少突胶质细胞功能障碍。
Int J Mol Sci. 2020 Mar 31;21(7):2395. doi: 10.3390/ijms21072395.
3
Coxsackievirus B3 Infection of Human Neural Progenitor Cells Results in Distinct Expression Patterns of Innate Immune Genes.
在数据稀疏的情况下,3' RNA测序比标准RNA测序更具优势,但在识别模式生物中的毒性途径方面则较差。
Front Bioinform. 2023 Jul 27;3:1234218. doi: 10.3389/fbinf.2023.1234218. eCollection 2023.
4
Technical assessment of different extraction methods and transcriptome profiling of RNA isolated from small volumes of blood.不同提取方法的技术评估及小体积血液中 RNA 的转录组谱分析。
Sci Rep. 2023 Mar 3;13(1):3598. doi: 10.1038/s41598-023-30629-5.
5
Application of the 3' mRNA-Seq using unique molecular identifiers in highly degraded RNA derived from formalin-fixed, paraffin-embedded tissue.使用独特分子标识符的3' mRNA测序在源自福尔马林固定石蜡包埋组织的高度降解RNA中的应用
BMC Genomics. 2021 Oct 24;22(1):759. doi: 10.1186/s12864-021-08068-1.
柯萨奇病毒 B3 感染人神经祖细胞导致固有免疫基因表达模式的显著差异。
Viruses. 2020 Mar 17;12(3):325. doi: 10.3390/v12030325.
4
tRNA 2'-O-methylation by a duo of TRM7/FTSJ1 proteins modulates small RNA silencing in Drosophila.TRM7/FTSJ1 蛋白双组分对 tRNA 2'-O-甲基化修饰调控果蝇中的小 RNA 沉默。
Nucleic Acids Res. 2020 Feb 28;48(4):2050-2072. doi: 10.1093/nar/gkaa002.
5
QuantSeq. 3' Sequencing combined with Salmon provides a fast, reliable approach for high throughput RNA expression analysis.QuantSeq 3' 测序与 Salmon 联合使用,为高通量 RNA 表达分析提供了一种快速、可靠的方法。
Sci Rep. 2019 Dec 11;9(1):18895. doi: 10.1038/s41598-019-55434-x.
6
Cytoplasmic functions of TDP-43 and FUS and their role in ALS.TDP-43 和 FUS 的细胞质功能及其在 ALS 中的作用。
Semin Cell Dev Biol. 2020 Mar;99:193-201. doi: 10.1016/j.semcdb.2019.05.023. Epub 2019 Jun 4.
7
A comparison between whole transcript and 3' RNA sequencing methods using Kapa and Lexogen library preparation methods.使用 Kapa 和 Lexogen 文库制备方法的全转录组和 3' RNA 测序方法比较。
BMC Genomics. 2019 Jan 7;20(1):9. doi: 10.1186/s12864-018-5393-3.
8
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin mice.在“FUSDelta14”基因敲入小鼠中,人源化突变FUS导致进行性运动神经元变性但无聚集。
Brain. 2017 Nov 1;140(11):2797-2805. doi: 10.1093/brain/awx248.
9
High-Resolution RNA Maps Suggest Common Principles of Splicing and Polyadenylation Regulation by TDP-43.高分辨率RNA图谱揭示TDP-43调控剪接和聚腺苷酸化的共同机制
Cell Rep. 2017 May 2;19(5):1056-1067. doi: 10.1016/j.celrep.2017.04.028.
10
The Function of the Mitochondrial Calcium Uniporter in Neurodegenerative Disorders.线粒体钙单向转运体在神经退行性疾病中的作用
Int J Mol Sci. 2017 Feb 10;18(2):248. doi: 10.3390/ijms18020248.