Department of Agroecology, Section of Crop Genetics and Biotechnology, Aarhus University, Forsøgsvej 1, DK-4200 Slagelse, Denmark.
Department of Biochemistry & Molecular Biology and VILLUM Center for Bioanalytical Sciences, University of Southern Denmark, Campusvej 55, DK-5230 Odense M, Denmark.
Int J Mol Sci. 2020 Feb 24;21(4):1546. doi: 10.3390/ijms21041546.
Overexpression of phytoglobins (formerly plant hemoglobins) increases the survival rate of plant tissues under hypoxia stress by the following two known mechanisms: (1) scavenging of nitric oxide (NO) in the phytoglobin/NO cycle and (2) mimicking ethylene priming to hypoxia when NO scavenging activates transcription factors that are regulated by levels of NO and O in the N-end rule pathway. To map the cellular and metabolic effects of hypoxia in barley ( L., cv. Golden Promise), with or without priming to hypoxia, we studied the proteome and metabolome of wild type (WT) and hemoglobin overexpressing (HO) plants in normoxia and after 24 h hypoxia (WT24, HO24). The WT plants were more susceptible to hypoxia than HO plants. The chlorophyll a + b content was lowered by 50% and biomass by 30% in WT24 compared to WT, while HO plants were unaffected. We observed an increase in ROS production during hypoxia treatment in WT seedlings that was not observed in HO seedlings. We identified and quantified 9694 proteins out of which 1107 changed significantly in abundance. Many proteins, such as ion transporters, Ca-signal transduction, and proteins related to protein degradation were downregulated in HO plants during hypoxia, but not in WT plants. Changes in the levels of histones indicates that chromatin restructuring plays a role in the priming of hypoxia. We also identified and quantified 1470 metabolites, of which the abundance of >500 changed significantly. In summary the data confirm known mechanisms of hypoxia priming by ethylene priming and N-end rule activation; however, the data also indicate the existence of other mechanisms for hypoxia priming in plants.
植物血球素(原植物血红蛋白)的过表达通过以下两种已知机制提高植物组织在缺氧胁迫下的存活率:(1)在植物血球素/NO 循环中清除一氧化氮(NO),以及(2)在清除 NO 激活受 NO 和 O 水平调节的转录因子时模拟乙烯对缺氧的引发。为了研究大麦( L.,cv. Golden Promise)在有或没有缺氧引发的情况下缺氧的细胞和代谢效应,我们研究了野生型(WT)和血红蛋白过表达(HO)植物在常氧和 24 小时缺氧(WT24,HO24)下的蛋白质组和代谢组。与 HO 植物相比,WT 植物对缺氧更敏感。与 WT 相比,WT24 中叶绿素 a + b 含量降低了 50%,生物量降低了 30%,而 HO 植物则不受影响。我们观察到在 WT 幼苗中,在缺氧处理期间 ROS 产生增加,但在 HO 幼苗中未观察到。我们鉴定和定量了 9694 种蛋白质,其中 1107 种蛋白质的丰度发生了显著变化。在缺氧期间,许多蛋白质,如离子转运蛋白、Ca 信号转导和与蛋白质降解相关的蛋白质,在 HO 植物中下调,但在 WT 植物中没有下调。组蛋白水平的变化表明染色质重构在缺氧引发中起作用。我们还鉴定和定量了 1470 种代谢物,其中 >500 种代谢物的丰度发生了显著变化。总之,这些数据证实了乙烯引发和 N 端规则激活的已知缺氧引发机制;然而,这些数据也表明植物中存在其他的缺氧引发机制。