Alanazi Jowaher S, Latimer Jean J
Department of Pharmaceutical Sciences, Nova Southeastern University and AutoNation Breast Cancer Institute, Fort Lauderdale, FL, USA.
Methods Mol Biol. 2020;2102:509-528. doi: 10.1007/978-1-0716-0223-2_28.
Host cell reactivation (HCR) is a transfection-based assay in which intact cells repair damage localized to exogenous DNA. This chapter provides instructions for the application of this technique, using as an exemplar UV irradiation as a source of damage to a luciferase reporter plasmid. Through measurement of the activity of a successfully transcribed and translated reporter enzyme, the amount of damaged plasmid that a cell can "reactivate" or repair and express can be quantitated. Different DNA repair pathways can be analyzed by this technique by damaging the reporter plasmid in different ways. Since it involves repair of a transcriptionally active gene, when applied to UV damage the HCR assay measures the capacity of the host cells to perform transcription-coupled repair (TCR), a subset of the overall nucleotide excision repair pathway that specifically targets transcribed gene sequences. This method features two ways to perform the assay using expression vectors with luciferase and beta galactosidase, as well as with firefly luciferase and Renilla luciferase using the same luminometer.
宿主细胞再激活(HCR)是一种基于转染的检测方法,其中完整的细胞修复定位在外源DNA上的损伤。本章提供了该技术应用的说明,以紫外线照射作为对荧光素酶报告质粒造成损伤的来源为例。通过测量成功转录和翻译的报告酶的活性,可以定量细胞能够“再激活”或修复并表达的受损质粒的量。通过以不同方式损伤报告质粒,该技术可以分析不同的DNA修复途径。由于它涉及转录活性基因的修复,当应用于紫外线损伤时,HCR检测测量宿主细胞进行转录偶联修复(TCR)的能力,TCR是整体核苷酸切除修复途径的一个子集,专门针对转录的基因序列。该方法具有两种使用荧光素酶和β-半乳糖苷酶表达载体进行检测的方式,以及使用同一台发光计同时检测萤火虫荧光素酶和海肾荧光素酶的方式。