Normark Benjamin B
Department of Plant, Soil, and Insect Sciences and Graduate Program in Organismic and Evolutionary Biology, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Evolution. 2006 Apr;60(4):631-42.
The genetic systems of animals and plants are typically eumendelian. That is, an equal complement of autosomes is inherited from each of two parents, and at each locus, each parent's allele is equally likely to be expressed and equally likely to be transmitted. Genetic systems that violate any of these eumendelian symmetries are termed asymmetric and include parent-specific gene expression (PSGE), haplodiploidy, thelytoky, and related systems. Asymmetric genetic systems typically arise in lineages with close associations between kin (gregarious siblings, brooding, or viviparity). To date, different explanatory frameworks have been proposed to account for each of the different asymmetric genetic systems. Haig's kinship theory of genomic imprinting argues that PSGE arises when kinship asymmetries between interacting kin create conflicts between maternally and paternally derived alleles. Greater maternal than paternal relatedness within groups selects for more "abstemious" expression of maternally derived alleles and more "greedy" expression of paternally derived alleles. Here, I argue that this process may also underlie origins of haplodiploidy and many origins of thelytoky. The tendency for paternal alleles to be more "greedy" in maternal kin groups means that maternal-paternal conflict is not a zero-sum game: the maternal optimum will more closely correspond to the optimum for family groups and demes and for associated entities such as symbionts. Often in these circumstances, partial or complete suppression of paternal gene expression will evolve (haplodiploidy, thelytoky), or other features of the life cycle will evolve to minimize the conflict (monogamy, inbreeding). Maternally transmitted cytoplasmic elements and maternally imprinted nuclear alleles have a shared interest in minimizing agonistic interactions between female siblings and may cooperate to exclude the paternal genome. Eusociality is the most dramatic expression of the conflict-reducing effects of haplodiploidy, but its original and more widespread function may be suppression of intrafamilial cannibalism. In rare circumstances in which paternal gene products gain access to maternal physiology via a placenta, PSGE with greedy paternal gene expression can persist (e.g., in mammals).
动植物的遗传系统通常是孟德尔式的。也就是说,从双亲各自继承相等数量的常染色体,并且在每个基因座上,每个亲本的等位基因表达的可能性相同,传递的可能性也相同。违反这些孟德尔式对称性的遗传系统被称为不对称遗传系统,包括亲本特异性基因表达(PSGE)、单倍二倍体、产雌孤雌生殖及相关系统。不对称遗传系统通常出现在亲属之间联系紧密的谱系中(群居的兄弟姐妹、育雏或胎生)。迄今为止,已经提出了不同的解释框架来解释每种不同的不对称遗传系统。黑格的基因组印记亲缘理论认为,当相互作用的亲属之间的亲缘不对称导致母源和父源等位基因之间产生冲突时,PSGE就会出现。群体内母系亲缘关系大于父系亲缘关系,会选择母源等位基因更“节制”的表达和父源等位基因更“贪婪”的表达。在此,我认为这个过程也可能是单倍二倍体起源和许多产雌孤雌生殖起源的基础。父源等位基因在母系亲属群体中更“贪婪”的倾向意味着母系-父系冲突不是一场零和博弈:母系最优解将更接近家族群体、种群以及共生体等相关实体的最优解。在这些情况下,父源基因表达的部分或完全抑制往往会进化出来(单倍二倍体、产雌孤雌生殖),或者生命周期的其他特征也会进化以尽量减少冲突(一夫一妻制、近亲繁殖)。母系传递的细胞质成分和母系印记的核等位基因在最小化雌性兄弟姐妹之间的对抗性相互作用方面有着共同利益,并且可能会合作排除父本基因组。群居昆虫的社会行为是单倍二倍体减少冲突效应的最显著表现,但其最初且更广泛的功能可能是抑制家族内部的同类相食行为。在罕见的情况下,父源基因产物通过胎盘进入母本生理系统,具有贪婪父源基因表达的PSGE可能会持续存在(例如在哺乳动物中)。