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本文引用的文献

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A filter at the entrance of the Golgi that selects vesicles according to size and bulk lipid composition.高尔基体入口处的一种过滤器,可根据大小和总体脂质组成选择囊泡。
Elife. 2016 Jul 26;5:e16988. doi: 10.7554/eLife.16988.
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A Eukaryotic Sensor for Membrane Lipid Saturation.真核生物细胞膜脂饱和度传感器
Mol Cell. 2016 Jul 7;63(1):49-59. doi: 10.1016/j.molcel.2016.05.015. Epub 2016 Jun 16.
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Mga2 Transcription Factor Regulates an Oxygen-responsive Lipid Homeostasis Pathway in Fission Yeast.Mga2转录因子调控裂殖酵母中的氧响应脂质稳态途径。
J Biol Chem. 2016 Jun 3;291(23):12171-83. doi: 10.1074/jbc.M116.723650. Epub 2016 Apr 6.
4
Identification of Rbd2 as a candidate protease for sterol regulatory element binding protein (SREBP) cleavage in fission yeast.鉴定Rbd2为裂殖酵母中固醇调节元件结合蛋白(SREBP)裂解的候选蛋白酶。
Biochem Biophys Res Commun. 2015 Dec 25;468(4):606-10. doi: 10.1016/j.bbrc.2015.10.165. Epub 2015 Nov 3.
5
Endoplasmic Reticulum Exit of Golgi-resident Defective for SREBP Cleavage (Dsc) E3 Ligase Complex Requires Its Activity.内质网输出对固醇调节元件结合蛋白裂解(Dsc)E3连接酶复合物有缺陷的高尔基体驻留蛋白需要其活性。
J Biol Chem. 2015 Jun 5;290(23):14430-40. doi: 10.1074/jbc.M114.630863. Epub 2015 Apr 27.
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Membrane curvature at a glance.膜曲率一览。
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7
Subunit architecture of the Golgi Dsc E3 ligase required for sterol regulatory element-binding protein (SREBP) cleavage in fission yeast.裂殖酵母固醇调节元件结合蛋白(SREBP)切割所需的高尔基 Dsc E3 连接酶的亚基结构。
J Biol Chem. 2013 Jul 19;288(29):21043-21054. doi: 10.1074/jbc.M113.468215. Epub 2013 Jun 12.
8
Yeast sterol regulatory element-binding protein (SREBP) cleavage requires Cdc48 and Dsc5, a ubiquitin regulatory X domain-containing subunit of the Golgi Dsc E3 ligase.酵母甾醇调节元件结合蛋白 (SREBP) 的切割需要 Cdc48 和 Dsc5,后者是高尔基 Dsc E3 连接酶的一个含有泛素调节 X 结构域的亚基。
J Biol Chem. 2012 Jan 2;287(1):672-681. doi: 10.1074/jbc.M111.317370. Epub 2011 Nov 15.
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Yeast SREBP cleavage activation requires the Golgi Dsc E3 ligase complex.酵母 SREBP 切割激活需要高尔基 Dsc E3 连接酶复合物。
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10
Links between lipid homeostasis, organelle morphodynamics and protein trafficking in eukaryotic and plant secretory pathways.真核生物和植物分泌途径中脂质动态平衡、细胞器形态动力学和蛋白质运输之间的联系。
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酵母甾醇调节元件结合蛋白(SREBP)和Mga2转录因子的协同调节

Coordinate Regulation of Yeast Sterol Regulatory Element-binding Protein (SREBP) and Mga2 Transcription Factors.

作者信息

Burr Risa, Stewart Emerson V, Espenshade Peter J

机构信息

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

出版信息

J Biol Chem. 2017 Mar 31;292(13):5311-5324. doi: 10.1074/jbc.M117.778209. Epub 2017 Feb 15.

DOI:10.1074/jbc.M117.778209
PMID:28202541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5392677/
Abstract

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.

摘要

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。