黄酮类化合物富集根瘤假单胞菌,提高杨树的氮利用率和次生根生长能力

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Jiadong Wu, Sijia Liu, Haoyu Zhang, Sisi Chen, Jingna Si, Lin Liu, Yue Wang, Shuxian Tan, Yuxin Du, Zhelun Jin, Jianbo Xie, Deqiang Zhang
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引用次数: 0

摘要

植物的生长行为是遗传网络结构的一个功能。根系微生物组变异对植物功能性状的影响日益被人们所认识,但调控这种变异的遗传机制却很少被研究。本研究收集了白杨(leuces)、艾格罗斯(Aigeiros)、塔卡玛哈卡(Tacamahaca)和图兰加(Turanga) 4个类群的9种杨的根和根际土壤,获得了根的代谢物和转录数据,根际微生物群数据,并进行了全面的多组学分析。结果表明,与表现不佳的杨树相比,长势强的白杨根中含有更多的假单胞菌。此外,我们证实假单胞菌与tricin和芹菜素的生物合成密切相关,并确定GLABRA3 (GL3)基因对tricin的分泌至关重要。通过PopGL3和查尔酮合成酶(PopCHS4)的组成性转录提高毛霉素分泌,可驱动假单胞菌在根际定殖,进一步促进氮素贫乏土壤中杨树的生长、氮素获取和次生根发育。本研究揭示了植物-代谢物-微生物调控模式对杨树适应性的影响,并全面解码了tricin的关键调控机制,为揭示植物关键代谢物与转录组和根际微生物的相互作用提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Flavones enrich rhizosphere Pseudomonas to enhance nitrogen utilization and secondary root growth in Populus

Flavones enrich rhizosphere Pseudomonas to enhance nitrogen utilization and secondary root growth in Populus

Plant growth behavior is a function of genetic network architecture. The importance of root microbiome variation driving plant functional traits is increasingly recognized, but the genetic mechanisms governing this variation are less studied. Here, we collect roots and rhizosphere soils from nine Populus species belonging to four sections (Leuce, Aigeiros, Tacamahaca, and Turanga), generate metabolite and transcription data for roots and microbiota data for rhizospheres, and conduct comprehensive multi-omics analyses. We demonstrate that the roots of vigorous Leuce poplar enrich more Pseudomonas, compared with the poorly performing poplar. Moreover, we confirm that Pseudomonas is strongly associated with tricin and apigenin biosynthesis and identify that gene GLABRA3 (GL3) is critical for tricin secretion. The elevated tricin secretion via constitutive transcription of PopGL3 and Chalcone synthase (PopCHS4) can drive Pseudomonas colonization in the rhizosphere and further enhance poplar growth, nitrogen acquisition, and secondary root development in nitrogen-poor soil. This study reveals that plant-metabolite-microbe regulation patterns contribute to the poplar fitness and thoroughly decodes the key regulatory mechanisms of tricin, and provides insights into the interactions of the plant’s key metabolites with its transcriptome and rhizosphere microbes.

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来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
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