Historic breeding practices contribute to germplasm divergence in leaf specialized metabolism and ecophysiology in cultivated sunflower (Helianthus annuus).

IF 2.4 2区 生物学 Q2 PLANT SCIENCES American Journal of Botany Pub Date : 2024-11-01 DOI:10.1002/ajb2.16420
Jordan A Dowell, Alan W Bowsher, Amna Jamshad, Rahul Shah, John M Burke, Lisa A Donovan, Chase M Mason
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Abstract

Premise: The use of hybrid breeding systems to increase crop yields has been the cornerstone of modern agriculture and is exemplified in the breeding and improvement of cultivated sunflower (Helianthus annuus). However, it is poorly understood what effect supporting separate breeding pools in such systems, combined with continued selection for yield, may have on leaf ecophysiology and specialized metabolite variation.

Methods: We analyzed 288 lines of cultivated H. annuus to examine the genomic basis of several specialized metabolites and agronomically important traits across major heterotic groups.

Results: Heterotic group identity supports phenotypic divergences between fertility restoring and cytoplasmic male-sterility maintainer lines in leaf ecophysiology and specialized metabolism. However, the divergence is not associated with physical linkage to nuclear genes that support current hybrid breeding practices in cultivated H. annuus. Additionally, we identified four genomic regions associated with leaf ecophysiology and specialized metabolism that colocalize with previously identified QTLs for quantitative self-compatibility traits and with S-protein homolog (SPH) proteins, a recently discovered family of proteins associated with self-incompatibility and self/nonself recognition in Papaver rhoeas (common poppy) with suggested conserved downstream mechanisms among eudicots.

Conclusions: Further work is necessary to confirm the self-incompatibility mechanisms in cultivated H. annuus and their relationship to the integrative and polygenic architecture of leaf ecophysiology and specialized metabolism in cultivated sunflower. However, because self-compatibility is a derived quantitative trait in cultivated H. annuus, trait linkage to divergent phenotypic traits may have partially arisen as a potential unintended consequence of historical breeding practices and selection for yield.

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历史上的育种实践导致了栽培向日葵(Helianthus annuus)种质在叶片特化代谢和生态生理学方面的差异。
前提:利用杂交育种系统提高作物产量一直是现代农业的基石,栽培向日葵(Helianthus annuus)的育种和改良就是例证。然而,人们还不太了解在这种系统中支持独立的育种池,再加上持续的产量选择,会对叶片生态生理学和特殊代谢物变异产生什么影响:方法:我们分析了 288 个栽培鹅掌楸品系,研究了几个特化代谢物和重要农艺性状在主要杂交群体中的基因组基础:结果:异交群体特征支持生育力恢复系和细胞质雄性保持系在叶片生态生理学和特化代谢方面的表型差异。然而,这种差异与核基因的物理联系无关,而核基因支持当前栽培雌花的杂交育种实践。此外,我们还发现了四个与叶片生态生理学和特化代谢相关的基因组区域,这些区域与之前发现的定量自相容性性状的 QTLs 以及 S 蛋白同源物(SPH)蛋白共定位,SPH 蛋白是最近发现的与 Papaver rhoeas(普通罂粟)的自相容性和自我/非自我识别相关的蛋白家族,其下游机制在裸子植物中是保守的:有必要开展进一步的工作,以确认栽培向日葵的自相容性机制及其与栽培向日葵叶片生态生理学和特化代谢的综合和多基因结构之间的关系。然而,由于自相容性是栽培向日葵的一个衍生数量性状,与不同表型性状的性状联系可能是历史育种实践和产量选择的一个潜在意外结果。
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来源期刊
American Journal of Botany
American Journal of Botany 生物-植物科学
CiteScore
4.90
自引率
6.70%
发文量
171
审稿时长
3 months
期刊介绍: The American Journal of Botany (AJB), the flagship journal of the Botanical Society of America (BSA), publishes peer-reviewed, innovative, significant research of interest to a wide audience of plant scientists in all areas of plant biology (structure, function, development, diversity, genetics, evolution, systematics), all levels of organization (molecular to ecosystem), and all plant groups and allied organisms (cyanobacteria, algae, fungi, and lichens). AJB requires authors to frame their research questions and discuss their results in terms of major questions of plant biology. In general, papers that are too narrowly focused, purely descriptive, natural history, broad surveys, or that contain only preliminary data will not be considered.
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