• 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

一系列用于植物中蛋白质丰度比例分析的双报告载体。

A series of dual-reporter vectors for ratiometric analysis of protein abundance in plants.

作者信息

Khosla Aashima, Rodriguez-Furlan Cecilia, Kapoor Suraj, Van Norman Jaimie M, Nelson David C

机构信息

Department of Botany and Plant Sciences University of California Riverside CA USA.

Department of Genetics University of Georgia Athens GA USA.

出版信息

Plant Direct. 2020 Jun 21;4(6):e00231. doi: 10.1002/pld3.231. eCollection 2020 Jun.

DOI:10.1002/pld3.231
PMID:32582876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7306620/
Abstract

Ratiometric reporter systems enable comparisons of the abundance of a protein of interest, or "target," relative to a reference protein. Both proteins are encoded on a single transcript but are separated during translation. This arrangement bypasses the potential for discordant expression that can arise when the target and reference proteins are encoded by separate genes. We generated a set of 18 Gateway-compatible vectors termed pRATIO that combine a variety of promoters, fluorescent, and bioluminescent reporters, and 2A "self-cleaving" peptides. These constructs are easily modified to produce additional combinations or introduce new reporter proteins. We found that mScarlet-I provides the best signal-to-noise ratio among several fluorescent reporter proteins during transient expression experiments in . Firefly and Gaussia luciferase also produce high signal-to-noise in . As proof of concept, we used this system to investigate whether degradation of the receptor KAI2 after karrikin treatment is influenced by its subcellular localization. KAI2 is normally found in the cytoplasm and the nucleus of plant cells. In karrikin-induced degradation of KAI2 was only observed when it was retained in the nucleus. These vectors are tools to easily monitor in vivo the abundance of a protein that is transiently expressed in plants, and will be particularly useful for investigating protein turnover in response to different stimuli.

摘要

比率报告系统能够比较目标蛋白(即“靶标”)相对于参考蛋白的丰度。这两种蛋白都编码在单个转录本上,但在翻译过程中会分开。这种安排避免了靶标蛋白和参考蛋白由不同基因编码时可能出现的表达不一致问题。我们构建了一组18个与Gateway兼容的载体,称为pRATIO,它们结合了多种启动子、荧光和生物发光报告基因以及2A“自切割”肽。这些构建体易于修饰,以产生更多组合或引入新的报告蛋白。我们发现,在拟南芥的瞬时表达实验中,mScarlet-I在几种荧光报告蛋白中具有最佳的信噪比。萤火虫荧光素酶和海肾荧光素酶在拟南芥中也产生高信噪比。作为概念验证,我们使用该系统研究了卡里金处理后受体KAI2的降解是否受其亚细胞定位的影响。KAI2通常存在于植物细胞的细胞质和细胞核中。在拟南芥中,只有当KAI2保留在细胞核中时,才观察到卡里金诱导的KAI2降解。这些载体是在体内轻松监测植物中瞬时表达的蛋白质丰度的工具,对于研究蛋白质在不同刺激下的周转将特别有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/c1ed1407a5c6/PLD3-4-e00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/070e0bcf97f6/PLD3-4-e00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/9471c042f565/PLD3-4-e00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/3bb4bb2b8041/PLD3-4-e00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/c1ed1407a5c6/PLD3-4-e00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/070e0bcf97f6/PLD3-4-e00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/9471c042f565/PLD3-4-e00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/3bb4bb2b8041/PLD3-4-e00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/c1ed1407a5c6/PLD3-4-e00231-g004.jpg

相似文献

1
A series of dual-reporter vectors for ratiometric analysis of protein abundance in plants.一系列用于植物中蛋白质丰度比例分析的双报告载体。
Plant Direct. 2020 Jun 21;4(6):e00231. doi: 10.1002/pld3.231. eCollection 2020 Jun.
2
Ratiometric Measurement of Protein Abundance after Transient Expression of a Transgene in .转基因在……中瞬时表达后蛋白质丰度的比率测量
Bio Protoc. 2020 Sep 5;10(17):e3747. doi: 10.21769/BioProtoc.3747.
3
Reporter Gene-Facilitated Detection of Compounds in Leaf Extracts that Activate the Karrikin Signaling Pathway.报告基因辅助检测叶提取物中激活卡里金信号通路的化合物。
Front Plant Sci. 2016 Dec 2;7:1799. doi: 10.3389/fpls.2016.01799. eCollection 2016.
4
Bringing Plant Immunity to Light: A Genetically Encoded, Bioluminescent Reporter of Pattern-Triggered Immunity in .揭示植物免疫:一种基因编码的生物发光模式触发免疫报告基因
Mol Plant Microbe Interact. 2023 Mar;36(3):139-149. doi: 10.1094/MPMI-07-22-0160-TA. Epub 2023 Feb 7.
5
Gateway binary vectors with organelle-targeted fluorescent proteins for highly sensitive reporter assay in gene expression analysis of plants.用于植物基因表达分析中高灵敏度报告基因检测的细胞器靶向荧光蛋白的 Gateway 二元载体。
J Biotechnol. 2019 May 20;297:19-27. doi: 10.1016/j.jbiotec.2019.03.015. Epub 2019 Mar 19.
6
Development of a Gateway-compatible two-component expression vector system for plants.开发一种与 Gateway 兼容的植物双组份表达载体系统。
Transgenic Res. 2019 Dec;28(5-6):561-572. doi: 10.1007/s11248-019-00167-w. Epub 2019 Aug 21.
7
The Karrikin Receptor Karrikin Insensitive2 Positively Regulates Heat Stress Tolerance in Arabidopsis thaliana.卡里金受体卡里金不敏感2正向调控拟南芥的热胁迫耐受性。
Plant Cell Physiol. 2023 Jan 30;63(12):1914-1926. doi: 10.1093/pcp/pcac112.
8
Transient expression in Nicotiana benthamiana fluorescent marker lines provides enhanced definition of protein localization, movement and interactions in planta.在本氏烟草荧光标记系中的瞬时表达增强了植物中蛋白质定位、移动和相互作用的清晰度。
Plant J. 2009 Jul;59(1):150-62. doi: 10.1111/j.1365-313X.2009.03850.x. Epub 2009 Feb 26.
9
Building customizable auto-luminescent luciferase-based reporters in plants.在植物中构建可定制的自动发光荧光素酶报告基因。
Elife. 2020 Mar 25;9:e52786. doi: 10.7554/eLife.52786.
10
Construction and validation of improved triple fusion reporter gene vectors for molecular imaging of living subjects.用于活体分子成像的改进型三重融合报告基因载体的构建与验证
Cancer Res. 2007 Apr 1;67(7):3085-93. doi: 10.1158/0008-5472.CAN-06-2402.

引用本文的文献

1
An N-terminal domain specifies developmental control by the SMAX1-LIKE family of transcriptional regulators in .一个N端结构域决定了植物中SMAX1类转录调节因子家族的发育控制。
Proc Natl Acad Sci U S A. 2025 Jun 17;122(24):e2412793122. doi: 10.1073/pnas.2412793122. Epub 2025 Jun 10.
2
Genetically Encoded, Noise-Tolerant, Auxin Biosensors in Yeast.酵母中基因编码、抗噪声、生长素生物传感器。
ACS Synth Biol. 2024 Sep 20;13(9):2804-2819. doi: 10.1021/acssynbio.4c00186. Epub 2024 Aug 28.
3
Improved validation of protein interactions using bicistronic BiFC (Bi2FC).

本文引用的文献

1
Design principles of a minimal auxin response system.最小生长素反应系统的设计原则。
Nat Plants. 2020 May;6(5):473-482. doi: 10.1038/s41477-020-0662-y. Epub 2020 May 15.
2
Fluorescent reporters for functional analysis in rice leaves.用于水稻叶片功能分析的荧光报告基因。
Plant Direct. 2020 Feb 11;4(2):e00188. doi: 10.1002/pld3.188. eCollection 2020 Feb.
3
SMAX1/SMXL2 regulate root and root hair development downstream of KAI2-mediated signalling in Arabidopsis.SMAX1/SMXL2 通过调控 KAI2 介导的信号通路调节拟南芥的根和根毛发育。
使用双顺反子双分子荧光互补技术(Bi2FC)改进蛋白质相互作用的验证。
Physiol Mol Biol Plants. 2024 Jul;30(7):1047-1054. doi: 10.1007/s12298-024-01477-y. Epub 2024 Jul 2.
4
Optimizing Promoters and Subcellular Localization for Constitutive Transgene Expression in Marchantia polymorpha.优化启动子和亚细胞定位以实现地钱中组成型转基因表达。
Plant Cell Physiol. 2024 Sep 3;65(8):1298-1309. doi: 10.1093/pcp/pcae063.
5
Quantitative Estimation of Promoter Activity in Cannabis sativa Using Agroinfiltration-Based Transient Gene Expression.利用基于农杆菌浸润的瞬时基因表达技术定量评估大麻中的启动子活性。
Methods Mol Biol. 2024;2787:245-253. doi: 10.1007/978-1-0716-3778-4_16.
6
Gene Stacking and Stoichiometric Expression of ER-Targeted Constructs Using "2A" Self-Cleaving Peptides.使用“2A”自我切割肽进行 ER 靶向构建体的基因叠加和化学计量表达。
Methods Mol Biol. 2024;2772:337-351. doi: 10.1007/978-1-0716-3710-4_26.
7
A quantitative autonomous bioluminescence reporter system with a wide dynamic range for Plant Synthetic Biology.用于植物合成生物学的具有宽动态范围的定量自主生物发光报告系统。
Plant Biotechnol J. 2024 Jan;22(1):37-47. doi: 10.1111/pbi.14146. Epub 2023 Oct 26.
8
The strigolactone receptor D14 targets SMAX1 for degradation in response to GR24 treatment and osmotic stress.独脚金内酯受体 D14 通过靶向 SMAX1 使其降解来响应 GR24 处理和渗透胁迫。
Plant Commun. 2022 Jan 31;3(2):100303. doi: 10.1016/j.xplc.2022.100303. eCollection 2022 Mar 14.
9
Rapid analysis of strigolactone receptor activity in a mutant.突变体中独脚金内酯受体活性的快速分析
Plant Direct. 2022 Mar 25;6(3):e389. doi: 10.1002/pld3.389. eCollection 2022 Mar.
10
KARRIKIN UP-REGULATED F-BOX 1 (KUF1) imposes negative feedback regulation of karrikin and KAI2 ligand metabolism in .KARRIKIN UP-REGULATED F-BOX 1 (KUF1) 对 KARRIKIN 和 KAI2 配体代谢施加负反馈调节作用。
Proc Natl Acad Sci U S A. 2022 Mar 15;119(11):e2112820119. doi: 10.1073/pnas.2112820119. Epub 2022 Mar 7.
PLoS Genet. 2019 Aug 29;15(8):e1008327. doi: 10.1371/journal.pgen.1008327. eCollection 2019 Aug.
4
I see the light! Fluorescent proteins suitable for cell wall/apoplast targeting in leaves.我看到曙光了!适用于叶片细胞壁/质外体靶向的荧光蛋白。
Plant Direct. 2019 Jan 17;3(1):e00112. doi: 10.1002/pld3.112. eCollection 2019 Jan.
5
Impairment in karrikin but not strigolactone sensing enhances root skewing in Arabidopsis thaliana.卡里卡丁感应受损而非独脚金内酯感应增强拟南芥根系偏斜。
Plant J. 2019 May;98(4):607-621. doi: 10.1111/tpj.14233. Epub 2019 Mar 11.
6
Polar vacuolar distribution is essential for accurate asymmetric division of zygotes.极性液泡的分布对于合子的精确不对称分裂是必不可少的。
Proc Natl Acad Sci U S A. 2019 Feb 5;116(6):2338-2343. doi: 10.1073/pnas.1814160116. Epub 2019 Jan 16.
7
Shining Light on the Secreted Luciferases of Marine Copepods: Current Knowledge and Applications.揭示海洋桡足类分泌型荧光素酶的奥秘:当前的知识和应用。
Photochem Photobiol. 2019 May;95(3):705-721. doi: 10.1111/php.13077. Epub 2019 Feb 11.
8
An Effective Way of Producing Fully Assembled Antibody in Transgenic Tobacco Plants by Linking Heavy and Light Chains via a Self-Cleaving 2A Peptide.通过自我切割的2A肽连接重链和轻链在转基因烟草植株中产生完全组装抗体的有效方法。
Front Plant Sci. 2018 Sep 19;9:1379. doi: 10.3389/fpls.2018.01379. eCollection 2018.
9
Photophysical Behavior of mNeonGreen, an Evolutionarily Distant Green Fluorescent Protein.mNeonGreen 的光物理行为,一种进化上遥远的绿色荧光蛋白。
Biophys J. 2018 May 22;114(10):2419-2431. doi: 10.1016/j.bpj.2018.04.013. Epub 2018 Apr 27.
10
Using the 2A Protein Coexpression System: Multicistronic 2A Vectors Expressing Gene(s) of Interest and Reporter Proteins.使用2A蛋白共表达系统:表达目的基因和报告蛋白的多顺反子2A载体。
Methods Mol Biol. 2018;1755:31-48. doi: 10.1007/978-1-4939-7724-6_3.