Ana M Sanchez, Aye K Kyaw, Sara Nunes Violante, Angad Garg, Justin R Cross, Stewart Shuman
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Time-resolved profiling revealed that many key phosphometabolites were progressively depleted, including (i) NTPs, NDPs, and dNTPs; (ii) coenzyme A, NAD<sup>+</sup>, NADP<sup>+</sup>, NADH, and ADP-ribose; (iii) glycolysis pathway intermediates upstream of pyruvate; (iv) pentose phosphate pathway intermediates from 6-phosphogluconate to sedoheptulose-7-phosphate; (v) nucleotide sugars GDP-hexose, UDP-glucose/galactose, and UDP-GalNAc/GlcNAc; and (vi) phospholipid precursors glycerol-3-phosphate, CDP-choline, and glycerophosphocholine. By contrast, early Krebs cycle intermediates accumulated during phosphate starvation. Other metabolic changes included the following: (i) interdiction of <i>de novo</i> pyrimidine synthesis; (ii) depletion of <i>S</i>-adenosylmethionine and <i>S</i>-adenosylhomocysteine; (iii) transient accumulation of polyamine biosynthetic intermediates putrescine and 5-methylthioadenosine; (iv) accumulation of betaine (correlating with an increase in expression of <i>atd1</i> mRNA encoding aldehyde dehydrogenase); and (v) depletion of aminoadipate pathway intermediates 2-oxoadipate, 2-aminoadipate, and saccharopine. Replenishing phosphate after 24 h of starvation resulted in restoration of the pre-starvation metabolome (over 2 to 12 h) as cells exited quiescence and resumed growth.</p><p><strong>Importance: </strong>Fission yeast <i>Schizosaccharomyces pombe</i> is a valuable model system to study cellular phosphate homeostasis and the adaptive responses to chronic phosphate starvation. Previous analyses focused on changes in the fission yeast transcriptome and proteome during phosphate starvation-induced durable G0 quiescence. Here, we deployed metabolomics to survey the scope and temporal order of metabolite changes during 24 h of phosphate starvation and the kinetics of metabolic recovery after cells starved for 24 h are replenished with phosphate. 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Here, we characterize the metabolic responses of fission yeast to a 24 h interval of phosphate starvation, during which cells enter a state of G0 quiescence. Time-resolved profiling revealed that many key phosphometabolites were progressively depleted, including (i) NTPs, NDPs, and dNTPs; (ii) coenzyme A, NAD<sup>+</sup>, NADP<sup>+</sup>, NADH, and ADP-ribose; (iii) glycolysis pathway intermediates upstream of pyruvate; (iv) pentose phosphate pathway intermediates from 6-phosphogluconate to sedoheptulose-7-phosphate; (v) nucleotide sugars GDP-hexose, UDP-glucose/galactose, and UDP-GalNAc/GlcNAc; and (vi) phospholipid precursors glycerol-3-phosphate, CDP-choline, and glycerophosphocholine. By contrast, early Krebs cycle intermediates accumulated during phosphate starvation. 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引用次数: 0
摘要
无机磷酸盐是细胞从环境中获得的必需营养物,并被细胞内代谢产物和大分子吸收。在这里,我们描述了裂变酵母对磷酸盐饥饿间隔24小时的代谢反应,在此期间细胞进入G0静止状态。时间分辨分析显示,许多关键的磷代谢产物逐渐耗尽,包括(i) NTPs、ndp和dNTPs;辅酶A、NAD+、NADP+、NADH和adp核糖;(iii)丙酮酸上游的糖酵解途径中间体;(iv)戊糖磷酸途径中间体,从6-磷酸葡萄糖酸酯到sedo庚糖-7-磷酸;(v)核苷酸糖(gdp -己糖、udp -葡萄糖/半乳糖和UDP-GalNAc/GlcNAc);磷脂前体甘油-3-磷酸、cdp -胆碱和甘油磷胆碱。相比之下,早期克雷布斯循环中间体在磷酸盐饥饿期间积累。其他代谢变化包括:(i)禁止从头合成嘧啶;(ii) s -腺苷蛋氨酸和s -腺苷同型半胱氨酸耗竭;(iii)多胺生物合成中间体腐胺和5-甲基硫代腺苷的短暂积累;(iv)甜菜碱的积累(与编码醛脱氢酶的atd1 mRNA表达增加相关);氨基己二酸途径中间体2-氧己二酸、2-氨基己二酸和糖精的耗竭。在饥饿24小时后补充磷酸盐,导致饥饿前代谢组恢复(超过2至12小时),细胞退出静止并恢复生长。裂糖酵母(Schizosaccharomyces pombe)是研究细胞磷酸盐稳态和慢性磷酸盐饥饿适应性反应的一个有价值的模型系统。先前的分析集中在磷酸盐饥饿诱导的持久G0静止期间裂变酵母转录组和蛋白质组的变化。在这里,我们利用代谢组学研究了24小时磷酸盐饥饿期间代谢物变化的范围和时间顺序,以及饥饿24小时后细胞补充磷酸盐后代谢恢复的动力学。这些结果有助于对磷酸盐状态如何影响细胞周期、基因表达、代谢和按时间顺序寿命的多组学理解。
Fission yeast metabolome dynamics during phosphate starvation and replenishment.
Inorganic phosphate is an essential nutrient acquired by cells from their environment and assimilated into myriad intracellular metabolites and macromolecules. Here, we characterize the metabolic responses of fission yeast to a 24 h interval of phosphate starvation, during which cells enter a state of G0 quiescence. Time-resolved profiling revealed that many key phosphometabolites were progressively depleted, including (i) NTPs, NDPs, and dNTPs; (ii) coenzyme A, NAD+, NADP+, NADH, and ADP-ribose; (iii) glycolysis pathway intermediates upstream of pyruvate; (iv) pentose phosphate pathway intermediates from 6-phosphogluconate to sedoheptulose-7-phosphate; (v) nucleotide sugars GDP-hexose, UDP-glucose/galactose, and UDP-GalNAc/GlcNAc; and (vi) phospholipid precursors glycerol-3-phosphate, CDP-choline, and glycerophosphocholine. By contrast, early Krebs cycle intermediates accumulated during phosphate starvation. Other metabolic changes included the following: (i) interdiction of de novo pyrimidine synthesis; (ii) depletion of S-adenosylmethionine and S-adenosylhomocysteine; (iii) transient accumulation of polyamine biosynthetic intermediates putrescine and 5-methylthioadenosine; (iv) accumulation of betaine (correlating with an increase in expression of atd1 mRNA encoding aldehyde dehydrogenase); and (v) depletion of aminoadipate pathway intermediates 2-oxoadipate, 2-aminoadipate, and saccharopine. Replenishing phosphate after 24 h of starvation resulted in restoration of the pre-starvation metabolome (over 2 to 12 h) as cells exited quiescence and resumed growth.
Importance: Fission yeast Schizosaccharomyces pombe is a valuable model system to study cellular phosphate homeostasis and the adaptive responses to chronic phosphate starvation. Previous analyses focused on changes in the fission yeast transcriptome and proteome during phosphate starvation-induced durable G0 quiescence. Here, we deployed metabolomics to survey the scope and temporal order of metabolite changes during 24 h of phosphate starvation and the kinetics of metabolic recovery after cells starved for 24 h are replenished with phosphate. These results contribute to a multi-omics understanding of how phosphate status impacts cell cycle, gene expression, metabolism, and chronological lifespan.
期刊介绍:
mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.