Genomic co-localization of variation affecting agronomic and human gut microbiome traits in a meta-analysis of diverse sorghum.

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
Nate Korth, Qinnan Yang, Mallory J Van Haute, Michael C Tross, Bo Peng, Nikee Shrestha, Mackenzie Zwiener-Malcom, Ravi V Mural, James C Schnable, Andrew K Benson
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Abstract

Substantial functional metabolic diversity exists within species of cultivated grain crops that directly or indirectly provide more than half of all calories consumed by humans around the globe. While such diversity is the molecular currency used for improving agronomic traits, diversity is poorly characterized for its effects on human nutrition and utilization by gut microbes. Moreover, we know little about agronomic traits' potential tradeoffs and pleiotropic effects on human nutritional traits. Here, we applied a quantitative genetics approach using a meta-analysis and parallel genome-wide association studies of Sorghum bicolor traits describing changes in the composition and function of human gut microbe communities, and any of 200 sorghum seed and agronomic traits across a diverse sorghum population to identify associated genetic variants. A total of 15 multiple-effect loci (MEL) were initially found where different alleles in the sorghum genome produced changes in seed that affected the abundance of multiple bacterial taxa across 2 human microbiomes in automated in vitro fermentations. Next, parallel genome-wide studies conducted for seed, biochemical, and agronomic traits in the same population identified significant associations within the boundaries of 13/15 MEL for microbiome traits. In several instances, the colocalization of variation affecting gut microbiome and agronomic traits provided hypotheses for causal mechanisms through which variation could affect both agronomic traits and human gut microbes. This work demonstrates that genetic factors affecting agronomic traits in sorghum seed can also drive significant effects on human gut microbes, particularly bacterial taxa considered beneficial. Understanding these pleiotropic relationships will inform future strategies for crop improvement toward yield, sustainability, and human health.

高粱多样性荟萃分析中影响农艺学和人类肠道微生物组性状的基因组共定位变异。
栽培谷物作物直接或间接为全球人类提供了一半以上的热量,其物种内部存在着大量的功能代谢多样性。虽然这种多样性是用于改善农艺性状的分子货币,但多样性对人类营养和肠道微生物利用的影响却鲜为人知。此外,我们对农艺性状对人类营养性状的潜在权衡和多效应知之甚少。在此,我们采用定量遗传学方法,通过荟萃分析和并行的高粱双色性状全基因组关联研究,描述了人类肠道微生物群落组成和功能的变化,以及多样化高粱种群中 200 种高粱种子和农艺性状中的任何一种性状,以确定相关的遗传变异。最初共发现了 15 个多效应位点(MEL),在这些位点上,高粱基因组中的不同等位基因会导致种子发生变化,从而影响自动体外发酵中两个人类微生物群落中多个细菌类群的丰度。接下来,在同一人群中对种子、生化和农艺性状进行了平行的全基因组研究,在微生物组性状的 13/15 MEL 边界内发现了显著的关联。在一些情况下,影响肠道微生物组和农艺性状的变异的共定位为变异可能影响农艺性状和人类肠道微生物的因果机制提供了假设。这项工作表明,影响高粱种子农艺性状的遗传因素也会对人类肠道微生物,尤其是被认为有益的细菌类群产生重大影响。了解这些多效关系将为未来作物改良战略提供信息,从而提高产量、可持续性和人类健康。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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