The genetic basis of selfing rate evolution

被引:3
|
作者
Xu, Kuangyi [1 ]
机构
[1] Univ N Carolina, Dept Biol, Coker Hall,120 South Rd, Chapel Hill, NC 27599 USA
关键词
Adaptation; dominance; genetic variation; mating systems; pollen limitation; selfing; MATING SYSTEM SHIFTS; INBREEDING DEPRESSION; DELETERIOUS MUTATIONS; REPRODUCTIVE-SYSTEMS; POPULATION-GENETICS; PLANT REPRODUCTION; OUTCROSSING RATES; POLLEN LIMITATION; HALDANES SIEVE; FLOWER SIZE;
D O I
10.1111/evo.14480
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Evolution of selfing is common in plant populations, but the genetic basis of selfing rate evolution remains unclear. Although the effects of genetic properties on fixation for mating-unrelated alleles have been investigated, loci that modify the selfing rate (selfing modifiers) differ from mating-unrelated loci in several aspects. Using population genetic models, I investigate the genetic basis of selfing rate evolution. For mating-unrelated alleles, selfing promotes fixation only for recessive mutations, but for selfing modifiers, because the selection coefficient depends on the background selfing rate, selfing can promote fixation even for dominant modifiers. For mating-unrelated alleles, the fixation probability from standing variation is independent of dominance and decreases with an increased background selfing rate. However, for selfing modifiers, the fixation probability peaks at an intermediate selfing rate and when alleles are recessive, because a change of its selection coefficient necessarily involves a change of the inbreeding coefficient, because both depend on the level of inbreeding depression. Furthermore, evolution of selfing involving multiple modifier loci is more likely when selfing is controlled by few large-effect rather than many slight-effect modifiers. I discuss how these characteristics of selfing modifiers have implications for the unidirectional transition from outcrossing to selfing and other empirical patterns.
引用
收藏
页码:883 / 898
页数:16
相关论文
共 50 条
  • [31] Genetic recombination as a molecular basis for the evolution of arboviruses
    Strauss, JH
    Strauss, EG
    FACTORS IN THE EMERGENCE OF ARBOVIRUS DISEASES: EMERGING DISEASES, 1997, : 37 - 50
  • [32] Probing the genetic basis of human brain evolution
    Lahn, B.
    AMERICAN JOURNAL OF PRIMATOLOGY, 2005, 66 : 140 - 140
  • [33] EARLY EVOLUTION OF THE GENETIC BASIS FOR SOMA IN THE VOLVOCACEAE
    Hanschen, Erik R.
    Ferris, Patrick J.
    Michod, Richard E.
    EVOLUTION, 2014, 68 (07) : 2014 - 2025
  • [34] EVOLUTION OF SPERM SHORTAGE IN A SELFING HERMAPHORODITE
    BARKER, DM
    EVOLUTION, 1992, 46 (06) : 1951 - 1955
  • [35] Population Rescue through an Increase in the Selfing Rate under Pollen Limitation: Plasticity versus Evolution
    Xu, Kuangyi
    AMERICAN NATURALIST, 2023, 202 (03): : 337 - 350
  • [36] Partial Selfing Can Reduce Genetic Loads While Maintaining Diversity During Experimental Evolution
    Chelo, Ivo M.
    Afonso, Bruno
    Carvalho, Sara
    Theologidis, Ioannis
    Goy, Christine
    Pino-Querido, Ania
    Proulx, Stephen R.
    Teotonio, Henrique
    G3-GENES GENOMES GENETICS, 2019, 9 (09): : 2811 - 2821
  • [37] The evolution of flower allometry in selfing species
    Ushimaru, A
    Nakata, K
    EVOLUTIONARY ECOLOGY RESEARCH, 2002, 4 (08) : 1217 - 1227
  • [38] Genetic variation and selfing rate in Lychnis flos-cuculi along an industrial pollution gradient
    Dulya, Olesya V.
    Mikryukov, Vladimir S.
    NEW PHYTOLOGIST, 2016, 209 (03) : 1083 - 1095
  • [39] The mutation load under tetrasomic inheritance and its consequences for the evolution of the selfing rate in autotetraploid species
    Ronfort, J
    GENETICS RESEARCH, 1999, 74 (01) : 31 - 42
  • [40] Maintenance of Quantitative Genetic Variance Under Partial Self-Fertilization, with Implications for Evolution of Selfing
    Lande, Russell
    Porcher, Emmanuelle
    GENETICS, 2015, 200 (03) : 891 - 906