首页> 外文期刊>Journal of Radiation Research: Official Organ of the Japan Radiation Research Society >The establishment and characterization of cell lines stably expressing human Ku80 tagged with enhanced green fluorescent protein
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The establishment and characterization of cell lines stably expressing human Ku80 tagged with enhanced green fluorescent protein

机译:稳定表达人KU80标记的细胞系的建立与表征,标记为增强的绿色荧光蛋白

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摘要

The Ku protein is a complex of two subunits, Ku70 and KU80, and it plays a role in multiple nuclear processes, e.g., nonhomologous DNA-end-joining (NHEJ), chromosome maintenance, and transcription regulation. On the other hand, several studies have reported a cytoplasmic or cell surface localization of Ku in various cell types. The mechanism underlying the regulation of all the diverse functions of Ku is still unclear, though the mechanism that regulates the nuclear localization of Ku70 and Ku80 appears to play, at least in part, a key role in regulating the physiological function of Ku. In this study, we generated cell lines expressing the human Ku80 tagged with the green fluorescent protein (GFP) color variants in Ku80-deficient cells, i.e., xrs-6 derived from CHO-K 1. Although Ku70, as well as Ku80, was undetectable in xrs-6 cells, it was seen in these transformants at a level similar to the level of CHO-K 1. Furthermore, etoposide- and radiosensitive phenotype of xrs-6 cells were corrected by an introduction of the tagged KU80. Moreover, the tagged Ku80 suppressed apoptosis triggered by DNA damage. These results demonstrate that fusion to the GFP color variants does not interfere with the functions of the Ku80 in the Ku-dependent DSB repair. Therefore, these transformants might be useful not only in the analysis of Ku80 behavior, but also in an analysis of the dynamics of the NHEJ repair process.
机译:KU蛋白是两个亚基,Ku70和Ku80的复合物,它在多种核过程中发挥作用,例如非症状DNA终端连接(NHEJ),染色体维持和转录调节。另一方面,几项研究报告了各种细胞类型的Ku细胞质或细胞表面定位。 ku所有各种功能规定的机制尚不清楚,尽管调节KU70和KU80核定位的机制似乎至少部分地发挥作用,在调节KU的生理功能方面发挥作用。在这项研究中,我们生成了在Ku80缺陷细胞中表达标记的人Ku80的细胞系,其中缺乏CHO-K1的XRS-6。虽然Ku70以及Ku80,但是在XRS-6细胞中未检测到,在这些转化体中观察到类似于CHO-K的水平的转化体中。此外,通过引入标记的KU80来校正XRS-6细胞的依托钠和放射敏感表型。此外,标记的KU80被DNA损伤触发的凋亡。这些结果表明,GFP颜色变体的融合不会干扰KU80在Ku的DSB修复中的功能。因此,这些转化体不仅可以在分析KU80行为的分析中,而且在分析NHEJ修复过程的分析中。

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