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利用双荧光素酶报告系统定量木质部特异性热稳定的精胺依赖的 SACL 转录物的翻译。

Quantification of Xylem-Specific Thermospermine-Dependent Translation of SACL Transcripts with Dual Luciferase Reporter System.

机构信息

Instituto de Biología Molecular y Celular de Plantas (CSIC-Universitat Politècnica de València), Valencia, Spain.

出版信息

Methods Mol Biol. 2024;2722:79-87. doi: 10.1007/978-1-0716-3477-6_6.

Abstract

Thermospermine (Tspm) is a polyamine found to play a crucial role in xylem development in Arabidopsis thaliana. Tspm promotes the translation of the SACL genes by counteracting the activity of a cis element in their 5'-leader region that suppresses the translation of the main ORF. Here we describe a method to test the Tspm-dependent translational regulation of the 5'-leader of the SACL mRNAs in Nicotiana benthamiana leaves and A. thaliana mesophyll protoplasts with a dual luciferase assay. The dual luciferase reporter system is used to assess gene expression and is based on the detection of the Firefly luciferase luminescence driven by a specific promoter. However, it can also be used to evaluate the cis elements found in 5'-leader that influence the translation of the main ORF in a transcript. We have used a modified version of the pGreenII 0800 LUC plasmid carrying a double 35S promoter, followed by a poly-linker sequence in phase with the Firefly luciferase gene (pGreen2x35SLUC) where the full 5'-leader sequence of SACL3 was cloned. This construct was used for Agrobacterium tumefaciens infiltration of N. benthamiana leaves and for transfection of A. thaliana mesophyll protoplasts, followed by mock or Tspm treatments. The resulting translation of the Firefly luciferase in these organisms and conditions was then tested by measuring luminescence with the dual luciferase assay and a luminometer. These experiments have allowed us to quantify the positive effect of Tspm in the translation of SACL3 transcripts.

摘要

热稳定多胺(Tspm)是一种多胺,被发现在拟南芥木质部发育中发挥关键作用。Tspm 通过抵消其 5' 前导区中抑制主要 ORF 翻译的顺式元件的活性,促进 SACL 基因的翻译。在这里,我们描述了一种在烟草Nicotiana benthamiana 叶片和拟南芥叶肉原生质体中使用双荧光素酶测定法测试 Tspm 依赖的 SACL mRNA 5' 前导翻译调节的方法。双荧光素酶报告系统用于评估基因表达,基于特定启动子驱动的萤火虫荧光素酶发光的检测。然而,它也可用于评估影响转录中主要 ORF 翻译的 5' 前导中的顺式元件。我们使用了经过修饰的 pGreenII 0800 LUC 质粒的一个版本,该质粒带有双 35S 启动子,随后是与萤火虫荧光素酶基因成相位的多接头序列(pGreen2x35SLUC),其中克隆了 SACL3 的完整 5' 前导序列。该构建体用于农杆菌侵染烟草Nicotiana benthamiana 叶片和拟南芥叶肉原生质体的转染,然后进行模拟或 Tspm 处理。然后通过使用双荧光素酶测定法和发光计测量这些生物体和条件下的萤火虫荧光素酶的发光来测试翻译。这些实验使我们能够量化 Tspm 在 SACL3 转录物翻译中的正效应。

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