Department of Biology, The Pennsylvania State University, University Park, PA 16802;
Arkansas Biosciences Institute, Arkansas State University, State University, AR 72467.
Proc Natl Acad Sci U S A. 2020 Feb 25;117(8):4243-4251. doi: 10.1073/pnas.1908707117. Epub 2020 Feb 11.
Host-parasite coevolution can maintain high levels of genetic diversity in traits involved in species interactions. In many systems, host traits exploited by parasites are constrained by use in other functions, leading to complex selective pressures across space and time. Here, we study genome-wide variation in the staple crop (L.) Moench and its association with the parasitic weed (Delile) Benth., a major constraint to food security in Africa. We hypothesize that geographic selection mosaics across gradients of parasite occurrence maintain genetic diversity in sorghum landrace resistance. Suggesting a role in local adaptation to parasite pressure, multiple independent loss-of-function alleles at sorghum are broadly distributed among African landraces and geographically associated with occurrence. However, low frequency of these alleles within -prone regions and their absence elsewhere implicate potential trade-offs restricting their fixation. is thought to cause resistance by changing stereochemistry of strigolactones, hormones that control plant architecture and below-ground signaling to mycorrhizae and are required to stimulate parasite germination. Consistent with trade-offs, we find signatures of balancing selection surrounding and other candidates from analysis of genome-wide associations with parasite distribution. Experiments with CRISPR-Cas9-edited sorghum further indicate that the benefit of -mediated resistance strongly depends on parasite genotype and abiotic environment and comes at the cost of reduced photosystem gene expression. Our study demonstrates long-term maintenance of diversity in host resistance genes across smallholder agroecosystems, providing a valuable comparison to both industrial farming systems and natural communities.
宿主-寄生虫协同进化可以维持物种相互作用中涉及的性状的高水平遗传多样性。在许多系统中,寄生虫利用的宿主性状受到其他功能的限制,导致跨时空的复杂选择压力。在这里,我们研究了主要粮食作物高粱(L.)Moench 的全基因组变异及其与寄生杂草(Delile)Benth. 的关联,后者是非洲粮食安全的主要制约因素。我们假设,寄生虫发生梯度上的地理选择镶嵌体维持了高粱地方品种抗性的遗传多样性。这表明在局部适应寄生虫压力方面发挥了作用,高粱多个独立的功能丧失等位基因在非洲地方品种中广泛分布,并与的发生存在地理关联。然而,这些等位基因在易感地区的低频率以及在其他地区的缺失暗示了潜在的权衡限制了它们的固定。据认为,通过改变独脚金内酯的立体化学来引起抗性,独脚金内酯是控制植物结构和地下信号到菌根的激素,对于刺激寄生虫萌发是必需的。与权衡一致,我们在分析与寄生虫分布相关的全基因组关联时,发现了围绕和其他候选基因的平衡选择的特征。使用 CRISPR-Cas9 编辑的高粱进行的实验进一步表明,介导的抗性的好处强烈依赖于寄生虫基因型和非生物环境,并且是以降低光合作用基因表达为代价的。我们的研究表明,在小农农业生态系统中,宿主抗性基因的多样性可以长期维持,这为工业农业系统和自然群落提供了有价值的比较。