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Regulation of one-carbon metabolism in arabidopsis: The N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation

机译:拟南芥中一碳代谢的调节:响应叶酸饥饿,胱硫醚γ-合酶的N末端调节域被切割。

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In all organisms, control of folate homeostasis is of vital importance to sustain the demand for one-carbon (C1) units that are essential in major metabolic pathways. In this study we induced folate deficiency in Arabidopsis ( Arabidopsis thaliana) cells by using two antifolate inhibitors. This treatment triggered a rapid and important decrease in the pool of folates with significant modification in the distribution of C1-substituted folate coenzymes, suggesting an adaptive response to favor a preferential shuttling of the flux of C1 units to the synthesis of nucleotides over the synthesis of methionine ( Met). Metabolic profiling of folate-deficient cells indicated important perturbation of the activated methyl cycle because of the impairment of Met synthases that are deprived of their substrate 5-methyl-tetrahydrofolate. Intriguingly, S-adenosyl-Met and Met pools declined during the initial period of folate starvation but were further restored to typical levels. Reestablishment of Met and S-adenosyl-Met homeostasis was concomitant with a previously unknown posttranslational modification that consists in the removal of 92 amino acids at the N terminus of cystathionine gamma-synthase (CGS), the first specific enzyme for Met synthesis. Rescue experiments and analysis of different stresses indicated that CGS processing is specifically associated with perturbation of the folates pool. Also, CGS processing involves chloroplastic serine-type proteases that are expressed in various plant species subjected to folate starvation. We suggest that a metabolic effector, to date unidentified, can modulate CGS activity in vivo through an interaction with the N-terminal domain of the enzyme and that removal of this domain can suppress this regulation.
机译:在所有生物中,控制叶酸稳态对维持对主要代谢途径必不可少的一碳(C1)单位的需求至关重要。在这项研究中,我们通过使用两种抗叶酸抑制剂诱导了拟南芥(Arabidopsis thaliana)细胞中的叶酸缺乏。这种处理触发了叶酸库的快速而重要的减少,并显着改变了C1取代的叶酸辅酶的分布,这表明了一种适应性反应,有利于C1单元通量对核苷酸合成的优先穿梭而不是核苷酸的合成。蛋氨酸(蛋氨酸)。叶酸缺乏细胞的代谢谱分析表明,由于缺乏其底物5-甲基-四氢叶酸的Met合酶的损伤,激活的甲基循环受到了严重干扰。有趣的是,在叶酸饥饿初期,S-腺苷-Met和Met池下降,但进一步恢复到典型水平。 Met和S-腺苷-Met稳态的重建与先前未知的翻译后修饰同时进行,该修饰包括去除胱氨酸Gamma合酶(CGS)N端N端的92个氨基酸,Met合成是第一个特异性酶。救援实验和对不同应力的分析表明,CGS加工与叶酸盐池的扰动特别相关。同样,CGS加工涉及在遭受叶酸饥饿的各种植物中表达的叶绿体丝氨酸型蛋白酶。我们建议迄今为止尚未确定的代谢效应子可以通过与酶的N末端结构域相互作用来调节体内CGS活性,并且去除该结构域可以抑制这种调节。

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