van Hooft Pim, Dougherty Eric R, Getz Wayne M, Greyling Barend J, Zwaan Bas J, Bastos Armanda D S
Resource Ecology Group, Wageningen University, Wageningen, The Netherlands.
Mammal Research Institute, Department of Zoology & Entomology, University of Pretoria, Hatfield, South Africa.
PLoS One. 2018 Feb 7;13(2):e0191481. doi: 10.1371/journal.pone.0191481. eCollection 2018.
In the African buffalo (Syncerus caffer) population of the Kruger National Park (South Africa) a primary sex-ratio distorter and a primary sex-ratio suppressor have been shown to occur on the Y chromosome. A subsequent autosomal microsatellite study indicated that two types of deleterious alleles with a negative effect on male body condition, but a positive effect on relative fitness when averaged across sexes and generations, occur genome-wide and at high frequencies in the same population. One type negatively affects body condition of both sexes, while the other acts antagonistically: it negatively affects male but positively affects female body condition. Here we show that high frequencies of male-deleterious alleles are attributable to Y-chromosomal distorter-suppressor pair activity and that these alleles are suppressed in individuals born after three dry pre-birth years, likely through epigenetic modification. Epigenetic suppression was indicated by statistical interactions between pre-birth rainfall, a proxy for parental body condition, and the phenotypic effect of homozygosity/heterozygosity status of microsatellites linked to male-deleterious alleles, while a role for the Y-chromosomal distorter-suppressor pair was indicated by between-sex genetic differences among pre-dispersal calves. We argue that suppression of male-deleterious alleles results in negative frequency-dependent selection of the Y distorter and suppressor; a prerequisite for a stable polymorphism of the Y distorter-suppressor pair. The Y distorter seems to be responsible for positive selection of male-deleterious alleles during resource-rich periods and the Y suppressor for positive selection of these alleles during resource-poor periods. Male-deleterious alleles were also associated with susceptibility to bovine tuberculosis, indicating that Kruger buffalo are sensitive to stressors such as diseases and droughts. We anticipate that future genetic studies on African buffalo will provide important new insights into gene fitness and epigenetic modification in the context of sex-ratio distortion and infectious disease dynamics.
在南非克鲁格国家公园的非洲水牛(非洲野水牛)种群中,已证明在Y染色体上存在一种原发性性别比例畸变基因和一种原发性性别比例抑制基因。随后的一项常染色体微卫星研究表明,在同一群体中,全基因组范围内存在两种对雄性身体状况有负面影响,但在跨性别和世代平均时对相对适应性有正面影响的有害等位基因,且频率较高。其中一种对两性的身体状况都有负面影响,而另一种则具有拮抗作用:它对雄性身体状况有负面影响,但对雌性身体状况有正面影响。在这里,我们表明雄性有害等位基因的高频率归因于Y染色体畸变-抑制基因对的活动,并且这些等位基因在出生前经历三个干旱年份后出生的个体中受到抑制,可能是通过表观遗传修饰。出生前降雨量(代表亲代身体状况)与与雄性有害等位基因相关的微卫星纯合/杂合状态的表型效应之间的统计相互作用表明了表观遗传抑制,而Y染色体畸变-抑制基因对的作用则通过扩散前小牛的性别间遗传差异得以体现。我们认为,对雄性有害等位基因的抑制导致了Y畸变基因和抑制基因的负频率依赖选择;这是Y畸变-抑制基因对稳定多态性的前提条件。Y畸变基因似乎在资源丰富时期负责雄性有害等位基因的正选择,而Y抑制基因在资源匮乏时期负责这些等位基因的正选择。雄性有害等位基因还与牛结核病易感性相关,这表明克鲁格水牛对疾病和干旱等应激源敏感。我们预计,未来对非洲水牛的遗传学研究将在性别比例畸变和传染病动态的背景下,为基因适应性和表观遗传修饰提供重要的新见解。