鹰嘴豆优化生物固氮途径的遗传见解及其与抗病育种的相互作用。

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
S L Bithell, M A Asif, J Chowdhury, A K Kamiri, F Snijders, S Harden, K L Plett, J M Plett
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引用次数: 0

摘要

鹰嘴豆(Cicer arietinum)是一种全球重要的粮食豆类,需要提高产量稳定性,以解决粮食安全和农业土地流失问题。一种方法是通过与根瘤菌的共生来提高养分获取和生物抗逆性。为了支持多种有益性状的同时选择,我们试图确定在共生促进生长条件下和病原体存在时改善植物-微生物共生的数量性状位点(QTL)和相关基因。我们的目的是利用鹰嘴豆-中根瘤菌根瘤菌模型来鉴定与生物固氮(BNF)和养分获取相关的QTL,并通过疫霉根腐病(Phytophthora root rot, PRR)对不同基因型鹰嘴豆固氮(BNF)对宿主基因表达的影响,了解生物胁迫下促进生物固氮(BNF)持续的因素。用两个鹰嘴豆× C。在鹰嘴豆重组自交系(RIL)群体中,我们鉴定出了与BNF相关的QTL和几个与宏量和微量营养状况相关的QTL。从一组最具PRR抗性的RIL (n = 70)中,我们成功地鉴定出具有高PRR抗性的RIL和来自BNF的n。在三方(宿主:根瘤菌:病原体)互作条件下,虽然病原菌对根瘤菌丰度没有一致的影响,但prr抗性基因型的n同化基因保持较高的活性,而易感基因型则抑制这些基因。对鹰嘴豆中BNF遗传支持的进一步了解将有助于选择保持较高BNF和更抗病的材料,这可能共同提高鹰嘴豆的产量稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Insights Into Pathways Supporting Optimized Biological Nitrogen Fixation in Chickpea and Their Interaction With Disease Resistance Breeding.

In chickpea (Cicer arietinum), a globally important grain legume, improvements in yield stability are required to address food security and agricultural land loss. One approach is to improve both nutrient acquisition through symbiosis with rhizobial bacteria and biotic stress resistance. To support the simultaneous selection of multiple beneficial traits, we sought to identify quantitative trait loci (QTL) and genes linked to improved plant-microbe symbiosis both under symbiosis-promotive growth conditions and when pathogens are present. Our aims were to use the chickpea-Mesorhizobium rhizobial model to identify QTL associated with biological nitrogen fixation (BNF) and nutrient acquisition and understand factors promotive of sustained BNF under biotic stress through the impact of Phytophthora root rot (PRR) on BNF across chickpea genotypes on host gene expression. Using two chickpea × C. echinospermum recombinant inbred line (RIL) populations, we identified QTL associated with BNF and several associated with macro- and micro-nutrient status of chickpea. From within a set of the most PRR-resistant RIL (n = 70), we successfully identified RIL with both high PRR resistance and N sourced from BNF. In conditions of the tripartite (host:rhizobia:pathogen) interaction, while there was no consistent pathogen impact on the abundance of Mesorhizobium in nodules, PRR-resistant genotypes maintained a higher activity of their N-assimilation genes, while susceptible genotypes repressed these genes. This improved understanding of the genetic support of BNF in chickpea will allow selection for material that maintains higher BNF and is more disease resistant, which together may improve yield stability in chickpea.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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