Vogel F, Crusio W E, Kovac C, Fryns J P, Freund M
Institut für Humangenetik und Anthropologie, Universität, Heidelberg, Federal Republic of Germany.
Hum Genet. 1990 Nov;86(1):25-32. doi: 10.1007/BF00205167.
The high incidence of the fra (X) syndrome (about 1:2000 male newborns) requires an explanation in view of the low fitness of mentally retarded hemizygous males and heterozygous females. In the past, it has been proposed that the mutation rate may be unusually high, and that mutations occur exclusively in male germ cells. According to an alternative hypothesis, a moderately high mutation rate might combine with a selective advantage of clinically unaffected heterozygotes. In earlier studies, such a combined hypothesis was shown to lead to plausible implications regarding mutation rate and fitness. Moreover, a mutation rate in male germ cells of the magnitude required by the exclusive mutation hypothesis was excluded by studies on comprehensive pedigree data. In this third study in the series, an increased fitness of heterozygous females is demonstrated directly by a comparison of the reproductive performance of heterozygotes with that of adequate controls (mothers and grandparents of Down's syndrome patients). Since, average numbers of children have decreased during recent decades in populations of industrialized countries, heterozygotes (mothers of affected probands and their female relatives in their own generation) were subdivided into those born before and after 1940. Moreover, sibship sizes of probands' mothers and fathers were analyzed separately for family branches in which the fra (X) trait segregated (mostly the maternal branch), or did not segregate (in most instances the paternal branch). In all four categories reproductive performance in heterozygotes was found to be higher than in the controls. This difference was significant statistically for two of the four groups; it was small and nonsignificant only for the parental family branch in which the fra (X) mutant did not segregate and for mothers born after 1940. Fitness estimates ranged between 1.11 and 1.36. A higher incidence of dizygotic twinning suggests a biological component for this increased fertility. On the other hand, fra (X) families have a significantly lower social status than the controls. This suggests a socio-psychological component of their higher fertility. Apparently, both components contribute to their fertility; at present, their relative importance cannot be assessed.
鉴于智力发育迟缓的半合子男性和杂合子女性适应性较低,脆性X综合征的高发病率(约为1:2000男性新生儿)需要作出解释。过去曾有人提出,突变率可能异常高,且突变仅发生在男性生殖细胞中。根据另一种假设,中等程度的高突变率可能与临床未受影响的杂合子的选择优势相结合。在早期研究中,这种综合假设被证明会产生关于突变率和适应性的合理推断。此外,对综合系谱数据的研究排除了仅突变假设所要求的男性生殖细胞中的突变率。在该系列的第三项研究中,通过将杂合子的生殖表现与适当对照(唐氏综合征患者的母亲和祖父母)进行比较,直接证明了杂合子女性适应性的提高。由于近几十年来工业化国家人口中平均子女数量有所下降,杂合子(受影响先证者的母亲及其同代女性亲属)被分为1940年之前和之后出生的两组。此外,分别分析了先证者母亲和父亲的同胞兄弟姐妹数量,这些家庭分支中脆性X特征发生分离(大多为母系分支)或未发生分离(在大多数情况下为父系分支)。在所有四类中,发现杂合子的生殖表现均高于对照组。在这四组中的两组中,这种差异具有统计学意义;仅在脆性X突变未发生分离的亲代家庭分支以及1940年之后出生的母亲中,差异较小且无统计学意义。适应性估计值在1.11至1.36之间。双卵双胎的发生率较高表明这种生育力增加存在生物学因素。另一方面,脆性X家庭的社会地位明显低于对照组。这表明其较高生育力存在社会心理因素。显然,这两个因素都对其生育力有影响;目前,它们的相对重要性尚无法评估。