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阿拉伯糖生物合成对拟南芥的耐盐性至关重要。

Arabinose biosynthesis is critical for salt stress tolerance in Arabidopsis.

机构信息

CAS Center for Excellence in Molecular Plant Sciences, Shanghai Center for Plant Stress Biology, Chinese Academy of Sciences, Shanghai, 201602, China.

Department of Horticulture and Landscape Architecture, Purdue University, West Lafayette, IN, 47907, USA.

出版信息

New Phytol. 2019 Oct;224(1):274-290. doi: 10.1111/nph.15867. Epub 2019 May 17.

DOI:10.1111/nph.15867
PMID:31009077
Abstract

The capability to maintain cell wall integrity is critical for plants to adapt to unfavourable conditions. l-Arabinose (Ara) is a constituent of several cell wall polysaccharides and many cell wall-localised glycoproteins, but so far the contribution of Ara metabolism to abiotic stress tolerance is still poorly understood. Here, we report that mutations in the MUR4 (also known as HSR8) gene, which is required for the biosynthesis of UDP-Arap in Arabidopsis, led to reduced root elongation under high concentrations of NaCl, KCl, NaNO , or KNO . The short root phenotype of the mur4/hsr8 mutants under high salinity is rescued by exogenous Ara or gum arabic, a commercial product of arabinogalactan proteins (AGPs) from Acacia senegal. Mutation of the MUR4 gene led to abnormal cell-cell adhesion under salt stress. MUR4 forms either a homodimer or heterodimers with its isoforms. Analysis of the higher order mutants of MUR4 with its three paralogues, MURL, DUR, MEE25, reveals that the paralogues of MUR4 also contribute to the biosynthesis of UDP-Ara and are critical for root elongation. Taken together, our work revealed the importance of the Ara metabolism in salt stress tolerance and also provides new insights into the enzymes involved in the UDP-Ara biosynthesis in plants.

摘要

维持细胞壁完整性的能力对于植物适应不利条件至关重要。L-阿拉伯糖(Ara)是几种细胞壁多糖和许多细胞壁定位糖蛋白的组成部分,但迄今为止,Ara 代谢对非生物胁迫耐受性的贡献仍知之甚少。在这里,我们报告说,拟南芥中 UDP-Arap 生物合成所需的 MUR4(也称为 HSR8)基因突变导致在高浓度 NaCl、KCl、NaNO3 或 KNO3 下根伸长减少。 mur4/hsr8 突变体在高盐下的短根表型可以通过外源性 Ara 或阿拉伯胶(来自 Acacia senegal 的阿拉伯半乳聚糖蛋白 (AGP) 的商业产品)挽救。MUR4 基因突变导致盐胁迫下细胞-细胞粘附异常。MUR4 形成同源二聚体或与同工型形成异源二聚体。对 MUR4 与其三个同源物 MURL、DUR 和 MEE25 的高级突变体的分析表明,MUR4 的同源物也有助于 UDP-Ara 的生物合成,并且对根伸长至关重要。总之,我们的工作揭示了 Ara 代谢在耐盐性中的重要性,并为植物中 UDP-Ara 生物合成涉及的酶提供了新的见解。

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