Walton K E, Styer D, Gruenstein E I
J Biol Chem. 1979 Aug 25;254(16):7951-60.
Two dimensional gel electrophoresis has been used to measure the degree of genetic polymorphism among the proteins of normal human fibroblasts. Autoradiographic analysis of the gel protein profiles from radioactively labeled cells allowed comparison of as many as 300 discrete polypeptides at a time. In addition, a newly developed technique for double label autoradiography was used to increase the sensitivity of the system for detection of small differences in the protein profiles of different cell lines. Only about 1.2% of the proteins of different cell lines were found to differ in their electrophoretic mobility. This corresponds to an average heterozygosity of approximately 0.6%. Previous studies of genetic polymorphism using different methods of one-dimensional electrophoretic analysis have estimated the average heterozygosity of the human population at about 6.7%. Detailed mathematical analysis shows the variation of the observed from the expected number of differences to be statistically highly significant. While the reasons for this difference are not clear, the observation of low levels of genetic polymorphism on two-dimensional gels should enhance the usefulness of this technique for detection of altered proteins in inherited disease.
二维凝胶电泳已被用于测量正常人成纤维细胞蛋白质之间的遗传多态性程度。对来自放射性标记细胞的凝胶蛋白质谱进行放射自显影分析,一次可比较多达300种离散多肽。此外,一种新开发的双标记放射自显影技术被用于提高该系统检测不同细胞系蛋白质谱微小差异的灵敏度。发现不同细胞系中只有约1.2%的蛋白质在电泳迁移率上存在差异。这相当于平均杂合度约为0.6%。先前使用不同一维电泳分析方法对遗传多态性的研究估计人类群体的平均杂合度约为6.7%。详细的数学分析表明,观察到的差异数量与预期差异数量之间的变化在统计学上具有高度显著性。虽然这种差异的原因尚不清楚,但二维凝胶上低水平遗传多态性的观察结果应会提高该技术在检测遗传性疾病中蛋白质改变方面的实用性。