Burr Risa, Stewart Emerson V, Espenshade Peter J
From the Department of Cell Biology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
From the Department of Cell Biology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205
J Biol Chem. 2017 Mar 31;292(13):5311-5324. doi: 10.1074/jbc.M117.778209. Epub 2017 Feb 15.
The Mga2 and Sre1 transcription factors regulate oxygen-responsive lipid homeostasis in the fission yeast in a manner analogous to the mammalian sterol regulatory element-binding protein (SREBP)-1 and SREBP-2 transcription factors. Mga2 and SREBP-1 regulate triacylglycerol and glycerophospholipid synthesis, whereas Sre1 and SREBP-2 regulate sterol synthesis. In mammals, a shared activation mechanism allows for coordinate regulation of SREBP-1 and SREBP-2. In contrast, distinct pathways activate fission yeast Mga2 and Sre1. Therefore, it is unclear whether and how these two related pathways are coordinated to maintain lipid balance in fission yeast. Previously, we showed that Sre1 cleavage is defective in the absence of Here, we report that this defect is due to deficient unsaturated fatty acid synthesis, resulting in aberrant membrane transport. This defect is recapitulated by treatment with the fatty acid synthase inhibitor cerulenin and is rescued by addition of exogenous unsaturated fatty acids. Furthermore, sterol synthesis inhibition blocks Mga2 pathway activation. Together, these data demonstrate that Sre1 and Mga2 are each regulated by the lipid product of the other transcription factor pathway, providing a source of coordination for these two branches of lipid synthesis.
Mga2和Sre1转录因子以类似于哺乳动物固醇调节元件结合蛋白(SREBP)-1和SREBP-2转录因子的方式调节裂殖酵母中的氧响应脂质稳态。Mga2和SREBP-1调节三酰甘油和甘油磷脂的合成,而Sre1和SREBP-2调节固醇合成。在哺乳动物中,一种共享的激活机制允许对SREBP-1和SREBP-2进行协调调节。相比之下,不同的途径激活裂殖酵母的Mga2和Sre1。因此,尚不清楚这两条相关途径是否以及如何协调以维持裂殖酵母中的脂质平衡。此前,我们表明在缺乏[此处原文缺失相关内容]的情况下Sre1裂解存在缺陷。在此,我们报告该缺陷是由于不饱和脂肪酸合成不足,导致异常的膜转运。用脂肪酸合酶抑制剂浅蓝菌素处理可重现此缺陷,添加外源性不饱和脂肪酸可挽救此缺陷。此外,固醇合成抑制会阻断Mga2途径的激活。总之,这些数据表明Sre1和Mga2各自受另一个转录因子途径的脂质产物调节,为脂质合成的这两个分支提供了一种协调来源。