Bvindi Carol, Tang Liang, Lee Sanghun, Patrick Ryan M, Yee Zheng Rong, Mengiste Tesfaye, Li Ying
Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Purdue Center for Plant Biology, Purdue University, West Lafayette, IN, United States.
Front Plant Sci. 2022 Oct 12;13:1005077. doi: 10.3389/fpls.2022.1005077. eCollection 2022.
Histone posttranslational modifications shape the chromatin landscape of the plant genome and affect gene expression in response to developmental and environmental cues. To date, the role of histone modifications in regulating plant responses to environmental nutrient availability, especially in agriculturally important species, remains largely unknown. We describe the functions of two histone lysine methyltransferases, SET Domain Group 33 (SDG33) and SDG34, in mediating nitrogen (N) responses of shoots and roots in tomato. By comparing the transcriptomes of CRISPR edited tomato lines and with wild-type plants under N-supplied and N-starved conditions, we uncovered that SDG33 and SDG34 regulate overlapping yet distinct downstream gene targets. In response to N level changes, both SDG33 and SDG34 mediate gene regulation in an organ-specific manner: in roots, SDG33 and SDG34 regulate a gene network including () and () genes. In agreement with this, mutations in or abolish the root growth response triggered by an N-supply; In shoots, SDG33 and SDG34 affect the expression of photosynthesis genes and photosynthetic parameters in response to N. Our analysis thus revealed that SDG33 and SDG34 regulate N-responsive gene expression and physiological changes in an organ-specific manner, thus presenting previously unknown candidate genes as targets for selection and engineering to improve N uptake and usage in crop plants.
组蛋白翻译后修饰塑造了植物基因组的染色质景观,并响应发育和环境线索影响基因表达。迄今为止,组蛋白修饰在调节植物对环境养分有效性的反应中的作用,尤其是在农业重要物种中,仍然很大程度上未知。我们描述了两种组蛋白赖氨酸甲基转移酶,SET结构域组33(SDG33)和SDG34,在介导番茄地上部和根部氮(N)反应中的功能。通过比较在供应氮和缺氮条件下CRISPR编辑的番茄株系和野生型植物的转录组,我们发现SDG33和SDG34调节重叠但不同的下游基因靶点。响应氮水平变化,SDG33和SDG34均以器官特异性方式介导基因调控:在根部,SDG33和SDG34调节一个基因网络,包括()和()基因。与此一致,或中的突变消除了由氮供应引发的根生长反应;在地上部,SDG33和SDG34响应氮影响光合作用基因的表达和光合参数。因此,我们的分析表明,SDG33和SDG34以器官特异性方式调节氮响应基因表达和生理变化,从而呈现出以前未知的候选基因作为选择和工程改造的靶点,以提高作物植物对氮的吸收和利用。