Todor Horia, Gooding Jessica, Ilkayeva Olga R, Schmid Amy K
Department of Biology, Duke University, Durham, North Carolina, United States of America.
Sarah W. Stedman Nutrition and Metabolism Center, Duke Molecular Physiology Institute, Departments of Pharmacology and Cancer Biology and Medicine, Duke University Medical Center, Durham, North Carolina, United States of America.
PLoS One. 2015 Aug 18;10(8):e0135693. doi: 10.1371/journal.pone.0135693. eCollection 2015.
Previous work demonstrated that the TrmB transcription factor is responsible for regulating the expression of many enzyme-coding genes in the hypersaline-adapted archaeon Halobacterium salinarum via a direct interaction with a cis-regulatory sequence in their promoters. This interaction is abolished in the presence of glucose. Although much is known about the effects of TrmB at the transcriptional level, it remains unclear whether and to what extent changes in mRNA levels directly affect metabolite levels. In order to address this question, here we performed a high-resolution metabolite profiling time course during a change in nutrients using a combination of targeted and untargeted methods in wild-type and ΔtrmB strain backgrounds. We found that TrmB-mediated transcriptional changes resulted in widespread and significant changes to metabolite levels across the metabolic network. Additionally, the pattern of growth complementation using various purines suggests that the mis-regulation of gluconeogenesis in the ΔtrmB mutant strain in the absence of glucose results in low phosphoribosylpyrophosphate (PRPP) levels. We confirmed these low PRPP levels using a quantitative mass spectrometric technique and found that they are associated with a metabolic block in de novo purine synthesis, which is partially responsible for the growth defect of the ΔtrmB mutant strain in the absence of glucose. In conclusion, we show how transcriptional regulation of metabolism affects metabolite levels and ultimately, phenotypes.
先前的研究表明,TrmB转录因子通过与嗜盐古菌盐生盐杆菌中许多酶编码基因启动子的顺式调控序列直接相互作用,来负责调控这些基因的表达。在葡萄糖存在的情况下,这种相互作用会被消除。尽管人们对TrmB在转录水平的作用了解很多,但mRNA水平的变化是否以及在多大程度上直接影响代谢物水平仍不清楚。为了解决这个问题,我们在这里使用靶向和非靶向方法相结合,在野生型和ΔtrmB菌株背景下,对营养物质变化期间的代谢物进行了高分辨率的时间进程分析。我们发现,TrmB介导的转录变化导致整个代谢网络中代谢物水平发生广泛而显著的变化。此外,使用各种嘌呤进行生长互补的模式表明,在没有葡萄糖的情况下,ΔtrmB突变菌株中糖异生的失调导致磷酸核糖焦磷酸(PRPP)水平较低。我们使用定量质谱技术证实了这些低PRPP水平,并发现它们与从头合成嘌呤的代谢阻滞有关,这在一定程度上导致了ΔtrmB突变菌株在没有葡萄糖时的生长缺陷。总之,我们展示了代谢的转录调控如何影响代谢物水平并最终影响表型。