Am Nat. 2021 Mar;197(3):E89-E109. doi: 10.1086/712424. Epub 2021 Jan 8.
AbstractIn angiosperm self-incompatibility systems, pollen with an allele matching the pollen recipient at the self-incompatibility locus is rejected. Extreme allelic polymorphism is maintained by frequency-dependent selection favoring rare alleles. However, two challenges result in a chicken-or-egg problem for the spread of a new allele (a tightly linked haplotype in this case) under the widespread "collaborative non-self-recognition" mechanism. A novel pollen function mutation alone would merely grant compatibility with a nonexistent style function allele: a neutral change at best. A novel pistil function mutation alone could be fertilized only by pollen with a nonexistent pollen function allele: a deleterious change that would reduce seed set to zero. However, a pistil function mutation complementary to a previously neutral pollen mutation may spread if it restores self-incompatibility to a self-compatible intermediate. We show that novel haplotypes can also drive elimination of existing ones with fewer siring opportunities. We calculate relative probabilities of increase and collapse in haplotype number given the initial collection of incompatibility haplotypes and the population gene conversion rate. Expansion in haplotype number is possible when population gene conversion rate is large, but large contractions are likely otherwise. A Markov chain model derived from these expansion and collapse probabilities generates a stable haplotype number distribution in the realistic range of 10-40 under plausible parameters. However, smaller populations might lose many haplotypes beyond those lost by chance during bottlenecks.
摘要 在被子植物自交不亲和系统中,与自交不亲和位点花粉受体匹配的花粉被排斥。通过有利于稀有等位基因的频率依赖性选择来维持极端的等位基因多态性。然而,在广泛存在的“协作非自我识别”机制下,新等位基因(在这种情况下是紧密连锁的单倍型)的传播存在两个挑战,导致了一个先有鸡还是先有蛋的问题。单独的花粉功能突变只会赋予与不存在的柱头功能等位基因的相容性:充其量是一个中性变化。单独的柱头功能突变只能被不存在花粉功能等位基因的花粉受精:这是一个有害的变化,会将种子设定降低到零。然而,如果一个与以前中性花粉突变互补的柱头功能突变可以恢复自交不亲和性到自交亲和的中间状态,那么它就可以传播。我们表明,新的单倍型也可以通过减少父本机会来消除现有的单倍型。我们根据初始的不亲和单倍型集合和群体基因转换率来计算单倍型数量增加和减少的相对概率。当群体基因转换率较大时,单倍型数量可能会增加,但在其他情况下,较大的收缩是可能的。从这些扩展和收缩概率中得出的马尔可夫链模型在现实范围内(10-40)产生了一个稳定的单倍型数量分布,在合理的参数下。然而,较小的种群可能会在瓶颈期失去许多单倍型,超过随机丢失的数量。