源自HeLa细胞的一种异常形式的CD59

A. Davies, D. Vannais, B. Fernie, A. B. Wilson, D. Gustafson, C. Willers, C. Waldren
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摘要

我们从HeLa细胞文库中分离出CD59 cDNA,该cDNA编码CD59的突变形式,具有单碱基替换(G到T),将Arg55变为Met。由于该突变发生在CD59的假定活性位点附近,我们在中国仓鼠卵巢细胞中表达了该蛋白的异常形式,以测试其对功能的影响。我们发现突变不影响CD59的补体抑制活性。然而,功能阻断CD59单克隆抗体BRIC229和YTH 53.1识别的表位受到显著影响。G到T的替换导致了一个mn1限制位点的丢失,这使得PCR-RFLP分析成为可能。所有被研究的52名人类受试者和我们内部的HeLa细胞都是正常CD59序列的纯合子,这表明序列的改变不是由于一般人群的正常变异。因此,这种突变可能是在用于产生商业获得的cDNA文库的HeLa细胞系中自发产生的。
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An Aberrant Form of CD59 Derived from HeLa Cells
We isolated a CD59 cDNA from a HeLa cell library which encoded a mutated form of CD59, having a single base substitution (G to T) that changed Arg55 to Met. Since this mutation occurred in the vicinity of the putative active site of CD59, we expressed the aberrant form of the protein in Chinese hamster ovary cells in order to test for effects upon function. We found that the mutation did not influence complement inhibitory activity of CD59. However, the epitopes recognised by the function-blocking CD59 monoclonal antibodies BRIC229 and YTH 53.1 were significantly affected. The G to T substitution caused loss of an Mnl I restriction site which permitted PCR-RFLP analysis. All of 52 human subjects studied, and our in-house HeLa cells, were homozygous for the normal CD59 sequence, indicating that the altered sequence was not due to normal variation in the general population. Therefore this mutation probably arose spontaneously in the HeLa cell line used to generate the commercially obtained cDNA library.
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