遗传对女性不忠和人类性伴侣数量的影响:抗利尿激素受体基因(AVPR1A)作用的连锁和关联研究

Lynn F Cherkas, Elizabeth C Oelsner, Y T Mak, Anna Valdes, Tim D Spector
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引用次数: 77

摘要

与动物不同,基因对人类不忠的影响尚不清楚。我们在这里报告了一项大型研究,研究对象是1600多对未经挑选的英国女性双胞胎,她们秘密报告了以前的不忠事件、一生中性伴侣的总数以及对不忠的态度。我们的研究结果表明,不忠和性伴侣的数量都受到适度的遗传影响(分别为41%和38%),这两个特征之间的遗传相关性很强(47%)。相反,对不忠的态度受到共同和独特的环境影响,而不是遗传影响。全基因组连锁扫描发现了3个与不忠和性伴侣数量相关的暗含但不显著的连锁区域,分别位于染色体3、7和20上,最大LOD评分为2.46。我们没有成功地将不忠或性伴侣的数量与其他哺乳动物的性行为相关的基因位点——抗利尿激素受体基因联系起来。尽管如此,我们关于性不忠的遗传性和性伴侣数量的研究结果为人类性行为的某些进化理论提供了支持,也为该领域进一步的遗传和分子研究提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic influences on female infidelity and number of sexual partners in humans: a linkage and association study of the role of the vasopressin receptor gene (AVPR1A).

In humans, in contrast to animals, the genetic influences on infidelity are unclear. We report here a large study of over 1600 unselected United Kingdom female twin pairs who confidentially reported previous episodes of infidelity and total lifetime number of sexual partners, as well as attitudes towards infidelity. Our findings demonstrate that infidelity and number of sexual partners are both under moderate genetic influence (41% and 38% heritable, respectively) and the genetic correlation between these two traits is strong (47%). Conversely, attitudes towards infidelity are driven by shared and unique environmental, but not genetic, influences. A genome-wide linkage scan identified three suggestive but nonsignificant linkage areas associated with infidelity and number of sexual partners on chromosomes 3, 7 and 20 with a maximum LOD score of 2.46. We were unsuccessful in associating infidelity or number of sexual partners with a locus implicated in other mammals' sexual behavior, the vasopressin receptor gene. Nonetheless, our findings on the heritability of sexual infidelity and number of sexual partners provide support for certain evolutionary theories of human sexual behavior, as well as justifying further genetic and molecular research in this domain.

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