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首页> 外文期刊>Nature reviews Cancer >Integrated analysis of the yeast NADPH-regulator Stb5 reveals distinct differences in NADPH requirements and regulation in different states of yeast metabolism
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Integrated analysis of the yeast NADPH-regulator Stb5 reveals distinct differences in NADPH requirements and regulation in different states of yeast metabolism

机译:酵母NADPH-稳压器STB5的综合分析显示了酵母代谢不同状态下的NADPH要求和调节的明显差异

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摘要

The Saccharomyces cerevisiae transcription factor (TF) Stb5 is known to be involved in regulating NADPH generation. We explored its role by combining DNA binding studies with transcriptome analysis at four environmental conditions that were selected to cover a range of different metabolic states. Using ChIP-exo, DNA binding targets of Stb5 were found to confirm many previously proposed binding targets, in particular genes encoding enzymes involved in NADPH generation and the pentose-phosphate (PP) pathway. Transcriptome analysis of an STB5 deletion strain revealed transcriptional changes in direct regulation targets of Stb5, including several PP pathway genes as well as additional novel regulatory targets, but interestingly not including the proposed PP pathway flux controlling enzyme Zwf1. Consistently, NADPH levels were found to decrease significantly with STB5 deletion in cultures with aerobic, glucose metabolism. We also found reduced growth for the STB5 deletion strain in similar conditions as those with reduced NADPH levels, supporting a role for Stb5 in NADPH generation through the PP pathway. We finally explored the flux distribution by genome scale modelling simulations and found a decreased flux in both NADPH generating as well as consuming reactions in the STB5 deletion strain.
机译:已知酿酒酵母转录因子(TF)STB5参与调节NADPH生成。我们通过在选择的四种环境条件下将DNA结合研究与转录组分析结合在选择以覆盖一系列不同代谢状态的环境条件下探讨其作用。使用CHIP-EXO,发现STB5的DNA结合靶标以确认许多先前提出的结合靶标,特别是编码参与NADPH生成和磷酸磷酸(PP)途径的酶的基因。 STB5缺失应变的转录组分析显示了STB5直接调节靶标的转录变化,包括几种PP途径基因以及额外的新型调节靶标,但有趣的是不包括所提出的PP途径通量控制酶ZWF1。始终如一地,发现NADPH水平随着葡萄糖,葡萄糖代谢的培养物中的STB5缺失显着降低。我们还发现在类似条件下的STB5缺失菌株的增长降低,因为具有降低的NADPH水平,支持通过PP途径在NADPH中的STB5作用。我们最终通过基因组规模模拟模拟探索了助焊剂分布,并发现了NADPH产生的减少的通量以及STB5缺失菌株中的消耗反应。

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