Molecular mechanisms affected by boron deficiency in root and shoot meristems of plants.

IF 5.6 2区 生物学 Q1 PLANT SCIENCES
Liuyang Chu, Cay Christin Schäfer, Michaela S Matthes
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引用次数: 0

Abstract

Boron deficiency is an abiotic stress that negatively impacts plant growth and yield worldwide. Boron deficiency primarily affects the development of plant meristems, groups of stem cells critical for all postembryonic tissue growth. The link between boron and meristem development was first established in 1923, when boron's essentiality was discovered. It remains, however, unclear whether boron directly integrates into molecular meristem pathways. In addition to its stabilizing function in the primary cell wall, growing evidence suggests roles of boron in various molecular processes including phytohormone cascades. These indications help enhance a mechanistic understanding of why boron is crucial for proper meristem development. In this review we compile and discuss molecular pathways influenced by boron availability in Arabidopsis (Arabidopsis thaliana), maize (Zea mays), rice (Oryza sativa), and oilseed rape (Brassica napus) with a focus on the auxin-, ethylene-, and cytokinin-mediated hormone cascades. We particularly compare and contrast phenotypic and molecular adaptations of shoot and root meristems to boron deficiency and pinpoint tissue-specific differences.

植物根部和芽分生组织受缺硼影响的分子机制
缺硼是一种非生物胁迫,对全世界植物的生长和产量都有负面影响。缺硼主要影响植物分生组织的发育,分生组织是对胚后组织生长至关重要的干细胞群。硼与分生组织发育之间的联系最早是在 1923 年发现的。然而,硼是否直接参与分生组织的分子途径,目前仍不清楚。除了硼在初级细胞壁中的稳定功能外,越来越多的证据表明硼在各种分子过程(包括植物激素级联)中发挥作用。这些迹象有助于加深对硼为何对分生组织的正常发育至关重要的机理的理解。在这篇综述中,我们汇编并讨论了拟南芥(Arabidopsis thaliana)、玉米(Zea mays)、水稻(Oryza sativa)和油菜(Brassica napus)中受硼可用性影响的分子途径,重点是辅酶、乙烯和细胞分裂素介导的激素级联。我们特别比较和对比了芽和根分生组织对硼缺乏的表型和分子适应性,并指出了组织特异性差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
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