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产生不稳定血红蛋白或血红蛋白M的新发突变。二、人类最小核苷酸突变率的直接估计。

De novo mutations producing unstable Hbs or Hbs M. II. Direct estimates of minimum nucleotide mutation rates in man.

作者信息

Stamatoyannopoulos G, Nute P E

出版信息

Hum Genet. 1982;60(2):181-8. doi: 10.1007/BF00569709.

Abstract

Cases of unstable hemoglobin and hemoglobin M disease that have appeared as de novo mutants over a span of approximately 50 years were used to deriving minimal, direct estimates of mutation rates per nucleotide per generation in man. The estimates are based upon analysis of data related to 40 cases of unstable Hbs and 15 of Hbs M that arose in 13 countries. The estimated rate calculated using all de novo beta-gene mutants is 7.4 X 10(-9) per nucleotide per generation; that derived using de novo alpha-gene mutants is 10.0 X 10(-9). Subsequent calculations of mutation rates per alpha- and beta-chain gene and extrapolation of these rates to a hypothetical gene of 1000 nucleotides yield an estimated mutation rate of 8.6 X 10(-6) per 1000 nucleotides per generation. Even though some instances of false paternity may have biased these estimates in an upward direction, under-reporting of Hb M cases, and particularly of unstable hemoglobins, makes it likely that the cited values are minimal estimates of mutation rates at the molecular level.

摘要

在大约50年的时间里出现的作为新生突变体的不稳定血红蛋白和血红蛋白M病的病例,被用于对人类每代每个核苷酸的突变率进行最小化的直接估计。这些估计是基于对13个国家出现的40例不稳定血红蛋白病例和15例血红蛋白M病例相关数据的分析。使用所有新生β基因突变得出的估计率为每代每个核苷酸7.4×10⁻⁹;使用新生α基因突变得出的估计率为10.0×10⁻⁹。随后对每个α链和β链基因的突变率进行计算,并将这些率外推到一个假设的1000个核苷酸的基因,得出每代每1000个核苷酸的估计突变率为8.6×10⁻⁶。尽管一些错误认定父亲的情况可能使这些估计值向上偏差,但血红蛋白M病例,尤其是不稳定血红蛋白病例的报告不足,使得所引用的值很可能是分子水平突变率的最小估计值。

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