Todd Bridget L, Stewart Emerson V, Burg John S, Hughes Adam L, Espenshade Peter J
Department of Cell Biology, Johns Hopkins University School of Medicine, 725 N. Wolfe Street, Physiology 107B, Baltimore, Maryland 21205, USA.
Mol Cell Biol. 2006 Apr;26(7):2817-31. doi: 10.1128/MCB.26.7.2817-2831.2006.
Fission yeast sterol regulatory element binding protein (SREBP), called Sre1p, functions in an oxygen-sensing pathway to allow adaptation to fluctuating oxygen concentrations. The Sre1p-Scp1p complex responds to oxygen-dependent sterol synthesis as an indirect measure of oxygen availability. To examine the role of Sre1p in anaerobic gene expression in Schizosaccharomyces pombe, we performed transcriptional profiling experiments after a shift to anaerobic conditions for 1.5 h. Of the 4,940 genes analyzed, expression levels of 521 (10.5%) and 686 (13.9%) genes were significantly increased and decreased, respectively, under anaerobic conditions. Sre1p controlled 68% of genes induced > or = 2-fold. Oxygen-requiring biosynthetic pathways for ergosterol, heme, sphingolipid, and ubiquinone were primary targets of Sre1p. Induction of glycolytic genes and repression of mitochondrial oxidative phosphorylation genes largely did not require Sre1p. Using chromatin immunoprecipitation, we demonstrated that Sre1p acts directly at target gene promoters and stimulates its own transcription under anaerobic conditions. sre1+ promoter analysis identified two DNA elements that are both necessary and sufficient for oxygen-dependent, Sre1p-dependent transcription. Interestingly, these elements are homologous to sterol regulatory elements bound by mammalian SREBP, highlighting the evolutionary conservation between Sre1p and SREBP. We conclude that Sre1p is a principal activator of anaerobic gene expression, upregulating genes required for nonrespiratory oxygen consumption.
裂殖酵母固醇调节元件结合蛋白(SREBP),称为Sre1p,在氧感应途径中发挥作用,以适应波动的氧浓度。Sre1p-Scp1p复合物对氧依赖性固醇合成作出反应,作为氧可用性的间接指标。为了研究Sre1p在粟酒裂殖酵母厌氧基因表达中的作用,我们在转移至厌氧条件1.5小时后进行了转录谱实验。在分析的4940个基因中,厌氧条件下分别有521个(10.5%)和686个(13.9%)基因的表达水平显著增加和降低。Sre1p控制了68%诱导倍数≥2倍的基因。麦角固醇、血红素、鞘脂和泛醌的需氧生物合成途径是Sre1p的主要靶标。糖酵解基因的诱导和线粒体氧化磷酸化基因的抑制在很大程度上不需要Sre1p。通过染色质免疫沉淀,我们证明Sre1p直接作用于靶基因启动子,并在厌氧条件下刺激其自身转录。sre1 +启动子分析确定了两个DNA元件,它们对于氧依赖性、Sre1p依赖性转录既是必需的也是充分的。有趣的是,这些元件与哺乳动物SREBP结合的固醇调节元件同源,突出了Sre1p和SREBP之间的进化保守性。我们得出结论,Sre1p是厌氧基因表达的主要激活剂,上调非呼吸性氧消耗所需的基因。