Birky C W, Maruyama T, Fuerst P
Genetics. 1983 Mar;103(3):513-27. doi: 10.1093/genetics/103.3.513.
We developed population genetic theory for organelle genes, using an infinite alleles model appropriate for molecular genetic data, and considering the effects of mutation and random drift on the frequencies of selectively neutral alleles. The effects of maternal inheritance and vegetative segregation of organelle genes are dealt with by defining new effective gene numbers, and substituting these for 2N(e) in classical theory of nuclear genes for diploid organisms. We define three different effective gene numbers. The most general is N(lambda), defined as a function of population size, number of organelle genomes per cell, and proportions of genes contributed by male and female gametes to the zygote. In many organisms, vegetative segregation of organelle genomes and intracellular random drift of organelle gene frequencies combine to produce a predominance of homoplasmic cells within individuals in the population. Then, the effective number of organelle genes is N(eo), a simple function of the numbers of males and females and of the maternal and paternal contributions to the zygote. Finally, when the paternal contribution is very small, N( eo) is closely approximated by the number of females, N( f). Then if the sex ratio is 1, the mean time to fixation or loss of new mutations is approximately two times longer for nuclear genes than for organelle genes, and gene diversity is approximately four times greater. The difference between nuclear and organelle genes disappears or is reversed in animals in which males have large harems. The differences between nuclear and organelle gene behavior caused by maternal inheritance and vegetative segregation are generally small and may be overshadowed by differences in mutation rates to neutral alleles. For monoecious organisms, the effective number of organelle genes is approximately equal to the total population size N. We also show that a population can be effectively subdivided for organelle genes at migration rates which result in panmixis for nuclear genes, especially if males migrate more than females.
我们利用适用于分子遗传数据的无限等位基因模型,考虑突变和随机漂变对选择性中性等位基因频率的影响,建立了细胞器基因的群体遗传理论。通过定义新的有效基因数来处理细胞器基因的母系遗传和营养分离效应,并将其代入二倍体生物核基因经典理论中的2N(e)。我们定义了三种不同的有效基因数。最通用的是N(lambda),它被定义为群体大小、每个细胞中细胞器基因组数量以及雄配子和雌配子对合子贡献的基因比例的函数。在许多生物体中,细胞器基因组的营养分离和细胞器基因频率的细胞内随机漂变相结合,导致群体中个体内同质细胞占主导。然后,细胞器基因的有效数量是N(eo),它是雄性和雌性数量以及母本和父本对合子贡献的简单函数。最后,当父本贡献非常小时,N(eo)非常接近雌性数量N(f)。那么,如果性别比为1,新突变固定或丢失的平均时间对于核基因来说大约是细胞器基因的两倍,并且基因多样性大约大四倍。在雄性拥有大量妻妾的动物中,核基因和细胞器基因之间的差异消失或反转。由母系遗传和营养分离引起的核基因和细胞器基因行为之间的差异通常较小,可能会被中性等位基因突变率的差异所掩盖。对于雌雄同体的生物体,细胞器基因的有效数量大约等于总人口大小N。我们还表明,对于细胞器基因,群体可以在导致核基因随机交配的迁移率下有效地细分,特别是如果雄性比雌性迁移更多。