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[尼美根断裂综合征患者细胞经电离辐射后p53蛋白诱导的特异性特征]

[Specific features of p53 protein induction after ionizing radiation in cells of patients with Nijmegen breakage syndrome].

作者信息

Balmukhanov T S, Aĭtkhozhina N A, Matsuura S, Komatsu K, Weemas C

机构信息

Institute of Molecular Biology and Biochemistry, Almaty, 480012, Kazakhstan.

出版信息

Genetika. 2002 Jul;38(7):980-4.

Abstract

Synthesis of p53 and WAF1 (p21) proteins was studied in cells of patients with Nijmegen breakage syndrome (NBS) and of patients with ataxia telangiectasia (AT), as well as in normal cells with respect to their response to ionizing radiation (IR). In the NBS cells, the p53 protein was progressively accumulated with increasing radiation dose and reached the maximum 2 h after exposure to radiation at a dose of 5 Gy. The amount of p53 protein was consistently lower than that in normal cells, which was correlated with low content of the WAF1, the protein regulated by p53 at the level of transcription. Suboptimal induction of p53 observed in NBS cells was also characteristic of the AT cells, though the quantitative parameters of the protein synthesis in AT cells were intermediate relative to those in normal and NBS cells. In four NBS lines, the time schedule of p53 synthesis was similar to that observed in normal cells, whereas in AT cells, induction of p53 was significantly delayed as compared to control. In response to irradiation, the amount of p53 protein synthesized in patients with AT and NBS was significantly lower than that in normal cells. The results obtained, as well as the previously published medical and genetic evidence, suggest that the two diseases are of different origin and different genes are responsible for their development.

摘要

研究了尼曼匹克氏症(NBS)患者和共济失调毛细血管扩张症(AT)患者细胞中p53和WAF1(p21)蛋白的合成情况,以及正常细胞对电离辐射(IR)的反应。在NBS细胞中,p53蛋白随着辐射剂量的增加而逐渐积累,在接受5 Gy剂量辐射后2小时达到最大值。p53蛋白的量始终低于正常细胞,这与WAF1含量低有关,WAF1是一种在转录水平受p53调控的蛋白。在NBS细胞中观察到的p53诱导不足也是AT细胞的特征,尽管AT细胞中蛋白质合成的定量参数相对于正常细胞和NBS细胞处于中间水平。在四个NBS细胞系中,p53合成的时间进程与正常细胞中观察到的相似,而在AT细胞中,与对照相比,p53的诱导明显延迟。对辐射的反应中,AT和NBS患者合成的p53蛋白量明显低于正常细胞。所获得的结果以及先前发表的医学和遗传学证据表明,这两种疾病起源不同,其发展由不同基因负责。

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