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利用报告基因、比较基因组学和凝胶迁移试验对疫霉进行启动子分析与剖析

Promoter Analysis and Dissection Using Reporter Genes, Comparative Genomics, and Gel Shift Assays in Phytophthora.

作者信息

Vo Nguyen N T, Judelson Howard S

机构信息

Department of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.

出版信息

Methods Mol Biol. 2025;2892:1-21. doi: 10.1007/978-1-0716-4330-3_1.

Abstract

Transcriptional regulation allows cells to execute developmental programs, maintain homeostasis, and respond to intra- and extracellular signals. Central to these processes are promoters, which in eukaryotes are sequences upstream of genes that bind transcription factors (TFs) and which recruit RNA polymerase to initiate mRNA synthesis. Valuable tools for studying promoters include reporter genes, which can be used to indicate when and where genes are activated. Moreover, functional regions within promoters (typically TF binding sites) can be identified by integrating reporter assays with promoter mutagenesis. These sites may also be revealed through comparative genomics, or by the DNA-protein binding procedure known as a gel shift or electrophoretic mobility shift assay (EMSA). The latter can also be used to test if a specific TF binds a DNA target or assess the binding kinetics or affinity of the complex. In this chapter, we describe procedures for expressing reporter genes in Phytophthora, assaying reporter activity, identifying functional sites within promoters, and testing purified TFs or proteins within nuclear extracts for DNA binding.

摘要

转录调控使细胞能够执行发育程序、维持体内平衡并响应细胞内和细胞外信号。这些过程的核心是启动子,在真核生物中,启动子是基因上游的序列,可结合转录因子(TFs)并招募RNA聚合酶以启动mRNA合成。用于研究启动子的重要工具包括报告基因,可用于指示基因何时何地被激活。此外,启动子内的功能区域(通常是TF结合位点)可以通过将报告基因检测与启动子诱变相结合来鉴定。这些位点也可以通过比较基因组学或通过称为凝胶迁移或电泳迁移率变动分析(EMSA)的DNA-蛋白质结合程序来揭示。后者还可用于测试特定TF是否结合DNA靶标或评估复合物的结合动力学或亲和力。在本章中,我们描述了在疫霉中表达报告基因、检测报告基因活性、鉴定启动子内功能位点以及测试核提取物中纯化的TF或蛋白质与DNA结合的程序。

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