Arabidopsis root responses to salinity depend on pectin modification and cell wall sensing

Nora Gigli-Bisceglia, Eva van Zelm, W. Huo, J. Lamers, C. Testerink
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引用次数: 28

Abstract

Soil salinity is an increasing worldwide problem for agriculture, affecting plant growth and yield. To understand the molecular mechanisms activated in response to salt in plants, we investigated the Catharanthus roseus Receptor like Kinase 1 Like (CrRLK1L) family, which contains well described sensors previously shown to be involved in maintaining and sensing the structural integrity of the cell walls. We found that herk1the1-4 double mutants, lacking the function of the Arabidopsis thaliana Receptor like Kinase HERKULES1 combined with a gain-of-function allele of THESEUS1, phenocopied the phenotypes previously reported in plants lacking FERONIA (FER) function. We report that both fer-4 and herk1the1-4 mutants respond strongly to salt application, resulting in a more intense activation of early and late stress responses. We also show that salt triggers de-methyl esterification of loosely bound pectins, responsible for the activation of several salt response signaling pathways. Addition of calcium chloride or chemically inhibiting pectin methyl esterase (PME) activity reduced activation of the early signaling protein Mitogen Activated Protein Kinase 6 (MPK6) as well as amplitude of salt-induced marker gene induction. MPK6 is required for the full induction of the salt-induced gene expression markers we tested. The sodium specific root halotropism response on the other hand, appears independent of MPK6 or calcium application, and is only mildly influenced by the cell wall sensors FER/HERK1/THE1-4 or alteration of PME activity. We hypothesize a model where salt-triggered modification of pectin requires the functionality of FER alone or the HERK1/THE1 combination to attenuate salt responses. Collectively, our results show the complexity of salt stress responses and salt sensing mechanisms and their connection to cell wall modifications, responsible for several salt response pathways and ultimately plant resilience to salinity.
拟南芥根系对盐度的响应依赖于果胶修饰和细胞壁感应
土壤盐碱化是一个日益严重的全球性农业问题,影响着植物的生长和产量。为了了解植物对盐的反应激活的分子机制,我们研究了Catharanthus roseus Receptor like Kinase 1 like (CrRLK1L)家族,该家族包含之前被证明参与维持和感知细胞壁结构完整性的传感器。我们发现herk1the1-4双突变体缺乏拟南芥受体样激酶HERKULES1的功能,结合了THESEUS1的功能获得等位基因,表型上复制了先前报道的缺乏FERONIA (FER)功能的植物的表型。我们报道,fer4和herk1the1-4突变体对盐的施用反应强烈,导致更强烈的早期和晚期胁迫反应的激活。我们还表明,盐触发松散结合的果胶的去甲基酯化反应,负责激活几种盐反应信号通路。添加氯化钙或化学抑制果胶甲基酯酶(PME)活性降低了早期信号蛋白有丝分裂原活化蛋白激酶6 (MPK6)的激活以及盐诱导标记基因诱导的幅度。MPK6是我们测试的盐诱导基因表达标记的完全诱导所必需的。另一方面,钠特异性根嗜盐性反应似乎与MPK6或钙施用无关,仅受细胞壁传感器FER/HERK1/THE1-4或PME活性改变的轻微影响。我们假设一个模型,其中盐触发的果胶修饰需要FER单独或HERK1/THE1组合的功能来减弱盐反应。总的来说,我们的研究结果表明,盐胁迫反应和盐感知机制的复杂性及其与细胞壁修饰的联系,负责几种盐响应途径和最终植物对盐的恢复力。
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