Neel J V, Mohrenweiser H W, Meisler M H
Proc Natl Acad Sci U S A. 1980 Oct;77(10):6037-41. doi: 10.1073/pnas.77.10.6037.
The techniques of electrophoresis were used in a search for evidence of mutation affecting protein structure, the indicators being hemoglobin and a set of serum proteins and erythrocyte enzymes. Among 94,796 locus tests on Amerindians from Central and South America, there was no evidence for mutation. Among 105,649 locus tests on newborn infants in Ann Arbor, Michigan, there was also no evidence for mutation. We have previously failed to encounter any mutations in a series of 208,196 locus tests involving Japanese children [Neel, J. V., Satoh, C., Hamilton, H. B., Otake, M., Goriki, K., Kageoka, T., Fugita, M., Neriishi, S & Asakawa,J. (1980) Proc. Natl. Acad. Sci. USA 77, 4221-4225], and H. Harris, D. A. Hopkinson, and E. B. Robson [(1974) Ann. Hum. Genet. 37, 237-253] found no mutations in 113,478 locus tests on inhabitants of the United Kingdom. This failure to demonstrate any mutations of this type in a total of 522,119 locus tests excludes, at the 95% level of probability, a mutation rate greater than 0.6 X 10(-5)/locus per generation in this combination of populations.
电泳技术被用于寻找影响蛋白质结构的突变证据,指标是血红蛋白、一组血清蛋白和红细胞酶。在对中南美洲美洲印第安人的94,796次基因座检测中,没有发现突变证据。在密歇根州安阿伯市对新生儿的105,649次基因座检测中,也没有发现突变证据。我们之前在对208,196名日本儿童进行的一系列基因座检测中未能发现任何突变[尼尔,J. V.,佐藤,C.,汉密尔顿,H. B.,小竹,M.,五木,K.,影冈,T.,藤田,M.,根岸,S. & 浅川,J.(1980年)《美国国家科学院院刊》77, 4221 - 4225],并且H. 哈里斯、D. A. 霍普金森和E. B. 罗布森[(1974年)《人类遗传学杂志》37, 237 - 253]在对英国居民的113,478次基因座检测中未发现突变。在总共522,119次基因座检测中未能证明任何此类突变,在95%的概率水平上排除了该人群组合中每代每个基因座的突变率大于0.6×10⁻⁵的可能性。