通过单细胞转录组学研究生物固氮。

IF 5.6 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2024-11-20 DOI:10.1093/jxb/erae454
Wendell J Pereira, Daniel Conde, Noé Perron, Henry W Schmidt, Christopher Dervinis, Rafael E Venado, Jean-Michel Ané, Matias Kirst
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引用次数: 0

摘要

大量使用氮肥会对环境造成有害影响,因此社会必须探索可持续的替代方法。根瘤共生是固氮族中某些植物物种自然发生的过程,将根瘤共生工程化到非豆科作物中是一个很有前景的途径。单细胞转录组学的进步为在细胞水平剖析根瘤共生的分子机制提供了前所未有的机会。本综述总结了对Medicago truncatula、Lotus japonicus和Glycine max进行单细胞研究的主要发现。我们重点介绍了这些研究如何解决有关根瘤共生发展的基本问题,包括以下发现:单细胞转录组学揭示了根毛和皮层细胞在根瘤菌感染过程中的保守转录程序,表明豆科植物物种之间存在共同的感染途径。利用单细胞技术对确定性和非确定性结核进行表征,支持将固氮、同化和运输划分为不同的细胞群。单细胞转录组学数据帮助鉴定了新的根瘤共生基因,并为优先选择候选基因进行功能表征提供了新方法。通过对单细胞转录组学数据进行轨迹推断和 RNA 速度分析,可以重建根瘤共生过程中的细胞系和动态转录状态。
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Investigating biological nitrogen fixation via single-cell transcriptomics.

The extensive use of nitrogen fertilizers has detrimental environmental consequences, and it is fundamental for society to explore sustainable alternatives. One promising avenue is engineering root nodule symbiosis, a naturally occurring process in certain plant species within the nitrogen-fixing clade, into non-leguminous crops. Advancements in single-cell transcriptomics provide unprecedented opportunities to dissect the molecular mechanisms underlying root nodule symbiosis at the cellular level. This review summarizes key findings from single-cell studies in Medicago truncatula, Lotus japonicus, and Glycine max. We highlight how these studies address fundamental questions about the development of root nodule symbiosis, including the following findings: Single-cell transcriptomics has revealed a conserved transcriptional program in root hair and cortical cells during rhizobial infection, suggesting a common infection pathway across legume species. Characterization of determinate and indeterminate nodules using single-cell technologies supports the compartmentalization of nitrogen fixation, assimilation, and transport into distinct cell populations. Single-cell transcriptomics data has enabled the identification of novel root nodule symbiosis genes and provided new approaches for prioritizing candidate genes for functional characterization. Trajectory inference and RNA velocity analyses of single-cell transcriptomics data have allowed the reconstruction of cellular lineages and dynamic transcriptional states during root nodule symbiosis.

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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
期刊最新文献
Investigating biological nitrogen fixation via single-cell transcriptomics. Innovative modeling on the effects of low-temperature stress on rice yields. Accounting for the impact of genotype and environment on variation in leaf respiration of wheat in Mexico and Australia. Diverse roles of phytohormonal signaling in modulating plant-virus interaction. Phytochrome-interacting factors PIF4 and PIF5 directly regulate autophagy during leaf senescence in Arabidopsis.
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