College of Life Sciences, Hunan University, Changsha, 410082, China.
Key Laboratory of Protein Chemistry and Developmental Biology of the Ministry of Education, Hunan Normal University, Changsha, 410081, China.
Physiol Plant. 2019 Apr;165(4):728-745. doi: 10.1111/ppl.12763. Epub 2018 Aug 2.
Lectin receptor-like kinases (LecRKs) play important roles in the responses to adverse environment stress. Abscisic acid (ABA) is a plant hormone involved in plant growth, development and adverse environmental stress responses. Although some studies of ABA response LecRK genes have been reported, the molecular mechanisms of LecRKs regulation of downstream pathways under ABA induction are not well understood. The present study showed that LecRK-VI.4 responded to ABA and negatively regulated stomatal closure. Here, a quantitative phosphoproteomics approach based on mass spectrometry was employed to study the roles of LecRK-VI.4 in the ABA signaling pathway. Metal oxide affinity beads and C18 chromatography were used for phosphopeptide enrichment and separation. The isobaric tags for relative and absolute quantitation were used for profiling the phosphoproteome of mutant lecrk-vi.4-1 and wild-type Col-0 Arabidopsis under normal growth conditions or ABA treatments. In total, 475 unique phosphopeptides were quantified, including 81 phosphopeptides related to LecRK-VI.4 regulation. Gene ontology, protein-protein interaction and motif analysis were performed. The bioinformatics data showed that phosphorylated proteins regulated by LecRK-VI.4 had close relations with factors of stomatal function, which included aquaporin activity, H pump activity and the Ca concentration in the cytoplasm. These data have expanded our understanding of how LecRK-VI.4 regulates ABA-mediated stomatal movements.
凝集素受体样激酶(LecRKs)在应对不利环境胁迫的反应中发挥重要作用。脱落酸(ABA)是一种参与植物生长、发育和应对环境胁迫反应的植物激素。尽管已经报道了一些关于 ABA 响应 LecRK 基因的研究,但 ABA 诱导下 LecRKs 对下游途径的调控的分子机制尚不清楚。本研究表明 LecRK-VI.4 对 ABA 有响应,并负调控气孔关闭。在这里,采用基于质谱的定量磷酸化蛋白质组学方法研究了 LecRK-VI.4 在 ABA 信号通路中的作用。使用金属氧化物亲和珠和 C18 色谱法进行磷酸肽富集和分离。用等重同位素标记相对和绝对定量技术对正常生长条件或 ABA 处理下突变体 lecrk-vi.4-1 和野生型 Col-0 拟南芥的 LecRK-VI.4 磷酸蛋白质组进行了分析。共定量了 475 个独特的磷酸肽,包括 81 个与 LecRK-VI.4 调节相关的磷酸肽。进行了基因本体、蛋白质-蛋白质相互作用和基序分析。生物信息学数据表明,LecRK-VI.4 调节的磷酸化蛋白与气孔功能的因子密切相关,包括水通道蛋白活性、H+泵活性和细胞质中的 Ca2+浓度。这些数据扩展了我们对 LecRK-VI.4 如何调节 ABA 介导的气孔运动的理解。