Lange K, Gladstien K, Zatz M
Am J Hum Genet. 1978 Mar;30(2):180-9.
A revival of interest in Haldane's equilibrium theory for X-linked lethals has been stimulated by the introduction of accurate tests for the detection of female heterozygotes in Lesch-Nyhan disease. Application of these tests appears to indicate an excess of familial cases. This excess can be attributed to ascertainment bias, a difference in female and male mutation rates, genetic drift, and reproductive compensation. Reproductive compensation will be particularly effective in increasing the proportion of familial cases if (1) birth control is widespread; (2) selection against affected males acts in utero; (3) affected sons show symptoms at an early age; and (4) sons are more highly valued than daughters. We demonstrate how only a few generations of reproductive compensation are sufficient to achieve an approximate equilibrium between selection and mutation showing a high proportion of familial cases. We also discuss the random fluctuations around equilibrium caused by genetic drift.
对莱施-奈恩病女性杂合子进行精确检测的试验问世后,人们重新燃起了对霍尔丹X连锁致死平衡理论的兴趣。应用这些试验似乎表明家族性病例过多。这种过多可归因于确诊偏倚、雌雄突变率差异、遗传漂变和生殖补偿。如果(1)节育普遍;(2)对患病男性的选择在子宫内起作用;(3)患病儿子在幼年出现症状;(4)儿子比女儿更受重视,那么生殖补偿在增加家族性病例比例方面将特别有效。我们证明,仅几代的生殖补偿就足以在选择和突变之间实现近似平衡,从而显示出高比例的家族性病例。我们还讨论了由遗传漂变引起的围绕平衡的随机波动。