Department of Chemical and Biomolecular Engineering, Rice University, Houston, TX, USA.
Department of Biosciences, Rice University, Houston, TX, USA.
Methods Mol Biol. 2022;2378:45-67. doi: 10.1007/978-1-0716-1732-8_4.
The unfolded protein response (UPR) is a complex signal transduction pathway that remodels gene expression in response to proteotoxic stress in the endoplasmic reticulum (ER) and is linked to the development of a range of diseases, including Alzheimer's disease, diabetes, and several types of cancer. UPR induction is typically monitored by measuring the expression level of UPR marker genes. Most tools for quantifying gene expression, including DNA microarrays and quantitative PCR with reverse transcription (RT-PCR), produce snapshots of the cell transcriptome, but are not ideal for measurements requiring temporal resolution of gene expression dynamics. Reporter assays for indirect detection of the UPR typically rely on extrachromosomal expression of reporters under the control of minimal or synthetic regulatory sequences that do not recapitulate the native chromosomal context of the UPR target genes. To address the need for tools to monitor chromosomal gene expression that recapitulate gene expression dynamics from the native chromosomal context and generate a readily detectable signal output, we developed a gene signal amplifier platform that links transcriptional and post-translational regulation of a fluorescent output to the expression of a chromosomal gene marker of the UPR. The platform is based on a genetic circuit that amplifies the output signal with high sensitivity and dynamic resolution and is implemented through chromosomal integration of the gene encoding the main control element of the genetic circuit to link its expression to that of the target gene, thereby generating a platform that can be easily adapted to monitor any UPR target through integration of the main control element at the appropriate chromosomal locus. By recapitulating the transcriptional and translational control mechanisms underlying the expression of UPR targets with high sensitivity, this platform provides a novel technology for monitoring the UPR with superior sensitivity and dynamic resolution.
未折叠蛋白反应(UPR)是一种复杂的信号转导途径,它会响应内质网(ER)中的蛋白毒性应激,重塑基因表达,并与一系列疾病的发展有关,包括阿尔茨海默病、糖尿病和几种类型的癌症。UPR 的诱导通常通过测量 UPR 标记基因的表达水平来监测。包括 DNA 微阵列和带有反转录(RT-PCR)的定量 PCR 在内的大多数基因表达定量工具都可以生成细胞转录组的快照,但对于需要基因表达动力学的时间分辨率测量并不理想。用于间接检测 UPR 的报告基因检测通常依赖于在受最小或合成调控序列控制的染色体外表达报告基因,而这些序列不能再现 UPR 靶基因的天然染色体环境。为了解决需要监测从天然染色体环境中再现基因表达动力学并产生易于检测的信号输出的染色体基因表达的工具的需求,我们开发了一种基因信号放大器平台,该平台将荧光输出的转录和翻译后调节与 UPR 染色体基因标记的表达联系起来。该平台基于一个遗传电路,该电路通过高灵敏度和动态分辨率放大输出信号,并且通过将基因编码的主要控制元件的染色体整合来实现,从而将其表达与靶基因的表达联系起来,从而生成一个可以通过在适当的染色体位置整合主要控制元件来轻松适应监测任何 UPR 靶标的平台。通过高灵敏度地再现 UPR 靶标表达的转录和翻译后控制机制,该平台为监测 UPR 提供了一种具有卓越灵敏度和动态分辨率的新技术。