Groh Jeffrey S, Vik Diane C, Stevens Kristian A, Brown Patrick J, Langley Charles H, Coop Graham
Department of Evolution and Ecology, University of California, Davis.
Center for Population Biology, University of California, Davis.
bioRxiv. 2024 Feb 8:2023.12.23.573205. doi: 10.1101/2023.12.23.573205.
The maintenance of stable mating type polymorphisms is a classic example of balancing selection, underlying the nearly ubiquitous 50/50 sex ratio in species with separate sexes. One lesser known but intriguing example of a balanced mating polymorphism in angiosperms is heterodichogamy - polymorphism for opposing directions of dichogamy (temporal separation of male and female function in hermaphrodites) within a flowering season. This mating system is common throughout Juglandaceae, the family that includes globally important and iconic nut and timber crops - walnuts (), as well as pecan and other hickories (). In both genera, heterodichogamy is controlled by a single dominant allele. We fine-map the locus in each genus, and find two ancient (>50 Mya) structural variants involving different genes that both segregate as genus-wide trans-species polymorphisms. The locus maps to a ca. 20 kb structural variant adjacent to a probable trehalose phosphate phosphatase (), homologs of which regulate floral development in model systems. is differentially expressed between morphs in developing male flowers, with increased allele-specific expression of the dominant haplotype copy. Across species, the dominant haplotype contains a tandem array of duplicated sequence motifs, part of which is an inverted copy of the 3' UTR. These repeats generate various distinct small RNAs matching sequences within the 3' UTR and further downstream. In contrast to the single-gene locus, the heterodichogamy locus maps to a ca. 200-450 kb cluster of tightly linked polymorphisms across 20 genes, some of which have known roles in flowering and are differentially expressed between morphs in developing flowers. The dominant haplotype in pecan, which is nearly always heterozygous and appears to rarely recombine, shows markedly reduced genetic diversity and is over twice as long as its recessive counterpart due to accumulation of various types of transposable elements. We did not detect either genetic system in other heterodichogamous genera within Juglandaceae, suggesting that additional genetic systems for heterodichogamy may yet remain undiscovered.
维持稳定的交配型多态性是平衡选择的一个经典例子,是具有两性的物种中几乎普遍存在的50/50性别比例的基础。被子植物中一个鲜为人知但有趣的平衡交配多态性例子是异时雌雄异熟——在一个开花季节内,雌雄异熟(雌雄同体中雄性和雌性功能的时间分离)方向相反的多态性。这种交配系统在胡桃科中很常见,该科包括全球重要且具有代表性的坚果和木材作物——核桃(),以及山核桃和其他山胡桃()。在这两个属中,异时雌雄异熟由单个显性等位基因控制。我们在每个属中对该位点进行了精细定位,发现了两个古老的(>5000万年前)结构变异,涉及不同的基因,它们都作为全属范围的跨物种多态性分离。该位点映射到一个约20 kb的结构变异,与一个可能的海藻糖磷酸磷酸酶()相邻,其同源物在模型系统中调节花的发育。在发育中的雄花中,该基因在不同形态之间差异表达,显性单倍型拷贝的等位基因特异性表达增加。在不同物种中,显性单倍型包含一个重复序列基序的串联阵列,其中一部分是3'UTR的反向拷贝。这些重复产生了各种与3'UTR内和更下游序列匹配的不同小RNA。与单基因位点不同,异时雌雄异熟位点映射到一个跨越20个基因的约200 - 450 kb紧密连锁多态性簇,其中一些基因在开花中具有已知作用,并且在发育中的花的不同形态之间差异表达。山核桃中的显性单倍型几乎总是杂合的,似乎很少重组,其遗传多样性显著降低,并且由于各种类型转座元件的积累,其长度是隐性对应物的两倍多。我们在胡桃科的其他异时雌雄异熟属中未检测到这两种遗传系统,这表明可能还有其他未被发现的异时雌雄异熟遗传系统。