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Sec14 like PITPs couple lipid metabolism with phosphoinositide synthesis to regulate Golgi functionality.Sec14 样磷脂酰肌醇转移蛋白将脂质代谢与磷酸肌醇合成相结合,以调节高尔基体功能。
Subcell Biochem. 2012;59:271-87. doi: 10.1007/978-94-007-3015-1_9.
2
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3
The Sec14 superfamily and mechanisms for crosstalk between lipid metabolism and lipid signaling.Sec14 超家族与脂质代谢和脂质信号转导之间相互作用的机制。
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4
Functional anatomy of phospholipid binding and regulation of phosphoinositide homeostasis by proteins of the sec14 superfamily.Sec14超家族蛋白对磷脂结合的功能解剖及磷酸肌醇稳态的调控
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6
Phospholipid transfer protein Sec14 is required for trafficking from endosomes and regulates distinct trans-Golgi export pathways.磷脂转移蛋白Sec14是内体运输所必需的,并调节不同的反式高尔基体输出途径。
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The Sec14-superfamily and the regulatory interface between phospholipid metabolism and membrane trafficking.Sec14超家族以及磷脂代谢与膜运输之间的调控界面。
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9
In vitro lipid transfer assays of phosphatidylinositol transfer proteins provide insight into the in vivo mechanism of ligand transfer.磷脂酰肌醇转移蛋白的体外脂质转移分析为研究配体转移的体内机制提供了线索。
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J Lipid Res. 2016 Apr;57(4):650-62. doi: 10.1194/jlr.M066381. Epub 2016 Feb 26.

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Phosphatidylinositol-Phosphatidic Acid Exchange by Nir2 at ER-PM Contact Sites Maintains Phosphoinositide Signaling Competence.Nir2在内质网-质膜接触位点进行的磷脂酰肌醇-磷脂酸交换维持了磷酸肌醇信号传导能力。
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Phosphoinositides: tiny lipids with giant impact on cell regulation.磷酸肌醇:调控细胞的微小脂质,却具有巨大影响。
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Osbpl8 deficiency in mouse causes an elevation of high-density lipoproteins and gender-specific alterations of lipid metabolism.小鼠中 Osbpl8 的缺失会导致高密度脂蛋白升高,并出现性别特异性的脂质代谢改变。
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本文引用的文献

1
Osh proteins regulate phosphoinositide metabolism at ER-plasma membrane contact sites.Osh 蛋白在 ER-质膜接触位点调节磷酸肌醇代谢。
Cell. 2011 Feb 4;144(3):389-401. doi: 10.1016/j.cell.2010.12.034.
2
Resurrection of a functional phosphatidylinositol transfer protein from a pseudo-Sec14 scaffold by directed evolution.通过定向进化从伪 Sec14 支架中复活具有功能的磷脂酰肌醇转移蛋白。
Mol Biol Cell. 2011 Mar 15;22(6):892-905. doi: 10.1091/mbc.E10-11-0903. Epub 2011 Jan 19.
3
Phosphatidylinositol 4-phosphate controls both membrane recruitment and a regulatory switch of the Rab GEF Sec2p.磷脂酰肌醇 4-磷酸控制 Rab GEF Sec2p 的膜募集和调节开关。
Dev Cell. 2010 May 18;18(5):828-40. doi: 10.1016/j.devcel.2010.03.016.
4
Interaction between Sec7p and Pik1p: the first clue for the regulation of a coincidence detection signal.Sec7p 和 Pik1p 的相互作用:巧合检测信号调控的第一个线索。
Eur J Cell Biol. 2010 Aug;89(8):575-83. doi: 10.1016/j.ejcb.2010.02.004.
5
Acute manipulation of Golgi phosphoinositides to assess their importance in cellular trafficking and signaling.急性调控高尔基磷酸肌醇以评估其在细胞运输和信号转导中的重要性。
Proc Natl Acad Sci U S A. 2010 May 4;107(18):8225-30. doi: 10.1073/pnas.1000157107. Epub 2010 Apr 19.
6
PtdIns4P recognition by Vps74/GOLPH3 links PtdIns 4-kinase signaling to retrograde Golgi trafficking.PtdIns4P 通过 Vps74/GOLPH3 的识别将 PtdIns4-kinase 信号与逆行高尔基运输联系起来。
J Cell Biol. 2009 Dec 28;187(7):967-75. doi: 10.1083/jcb.200909063. Epub 2009 Dec 21.
7
Dual roles for the Drosophila PI 4-kinase four wheel drive in localizing Rab11 during cytokinesis.果蝇 PI 4-kinase 四驱动在胞质分裂过程中定位 Rab11 的双重作用。
J Cell Biol. 2009 Dec 14;187(6):847-58. doi: 10.1083/jcb.200908107.
8
Linking phospholipid flippases to vesicle-mediated protein transport.将磷脂翻转酶与囊泡介导的蛋白质运输联系起来。
Biochim Biophys Acta. 2009 Jul;1791(7):612-9. doi: 10.1016/j.bbalip.2009.03.004. Epub 2009 Mar 12.
9
Early stages of Golgi vesicle and tubule formation require diacylglycerol.高尔基体囊泡和小管形成的早期阶段需要二酰基甘油。
Mol Biol Cell. 2009 Feb;20(3):780-90. doi: 10.1091/mbc.e08-03-0256. Epub 2008 Nov 26.
10
Trans-Golgi network and endosome dynamics connect ceramide homeostasis with regulation of the unfolded protein response and TOR signaling in yeast.反式高尔基体网络和内体动力学将神经酰胺稳态与酵母中未折叠蛋白反应的调节及雷帕霉素靶蛋白信号传导联系起来。
Mol Biol Cell. 2008 Nov;19(11):4785-803. doi: 10.1091/mbc.e08-04-0426. Epub 2008 Aug 27.

Sec14 样磷脂酰肌醇转移蛋白将脂质代谢与磷酸肌醇合成相结合,以调节高尔基体功能。

Sec14 like PITPs couple lipid metabolism with phosphoinositide synthesis to regulate Golgi functionality.

作者信息

Mousley Carl J, Davison James M, Bankaitis Vytas A

机构信息

Department of Cell & Developmental Biology, Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, 27599-7090, Chapel Hill, NC, USA,

出版信息

Subcell Biochem. 2012;59:271-87. doi: 10.1007/978-94-007-3015-1_9.

DOI:10.1007/978-94-007-3015-1_9
PMID:22374094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5373100/
Abstract

An interface coordinating lipid metabolism with proteins that regulate membrane trafficking is necessary to regulate Golgi morphology and dynamics. Such an interface facilitates the membrane deformations required for vesicularization, forms platforms for protein recruitment and assembly on appropriate sites on a membrane surface and provides lipid co-factors for optimal protein activity in the proper spatio-temporally regulated manner. Importantly, Sec14 and Sec14-like proteins are a unique superfamily of proteins that sense specific aspects of lipid metabolism, employing this information to potentiate phosphoinositide production. Therefore, Sec14 and Sec14 like proteins form central conduits to integrate multiple aspects of lipid metabolism with productive phosphoinositide signaling.

摘要

协调脂质代谢与调节膜运输的蛋白质之间的界面对于调节高尔基体的形态和动力学是必要的。这样的界面促进了囊泡化所需的膜变形,在膜表面的适当位点形成蛋白质募集和组装的平台,并以适当的时空调节方式提供脂质辅助因子以实现最佳蛋白质活性。重要的是,Sec14和类Sec14蛋白是一类独特的蛋白质超家族,它们感知脂质代谢的特定方面,并利用这些信息增强磷脂酰肌醇的产生。因此,Sec14和类Sec14蛋白形成了核心通道,将脂质代谢的多个方面与有效的磷脂酰肌醇信号传导整合在一起。