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Phosphoinositide 5-phosphatase Fig 4p is required for both acute rise and subsequent fall in stress-induced phosphatidylinositol 3,5-bisphosphate levels.磷酸肌醇5-磷酸酶Fig 4p对于应激诱导的磷脂酰肌醇3,5-二磷酸水平的急性升高及随后的下降均是必需的。
Eukaryot Cell. 2006 Apr;5(4):723-31. doi: 10.1128/EC.5.4.723-731.2006.
2
The Vac14p-Fig4p complex acts independently of Vac7p and couples PI3,5P2 synthesis and turnover.Vac14p-Fig4p复合物独立于Vac7p发挥作用,并将磷脂酰肌醇-3,5-二磷酸(PI3,5P2)的合成与周转联系起来。
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Roles for a lipid phosphatase in the activation of its opposing lipid kinase.脂质磷酸酶在其相反脂质激酶激活中的作用。
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4
Osmotic stress-induced increase of phosphatidylinositol 3,5-bisphosphate requires Vac14p, an activator of the lipid kinase Fab1p.渗透胁迫诱导的磷脂酰肌醇3,5-二磷酸增加需要Vac14p,它是脂质激酶Fab1p的激活剂。
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5
Early protection to stress mediated by CDK-dependent PI3,5P signaling from the vacuole/lysosome.由液泡/溶酶体中依赖细胞周期蛋白依赖性激酶的PI3,5P信号介导的对压力的早期保护。
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Vacuole size control: regulation of PtdIns(3,5)P2 levels by the vacuole-associated Vac14-Fig4 complex, a PtdIns(3,5)P2-specific phosphatase.液泡大小控制:由与液泡相关的Vac14-Fig4复合物(一种PtdIns(3,5)P2特异性磷酸酶)对PtdIns(3,5)P2水平进行调控。
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A protein complex that regulates PtdIns(3,5)P2 levels.一种调节磷脂酰肌醇-3,5-二磷酸(PtdIns(3,5)P2)水平的蛋白质复合物。
EMBO J. 2009 Jan 21;28(2):86-7. doi: 10.1038/emboj.2008.270.
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Sac1 lipid phosphatase and Stt4 phosphatidylinositol 4-kinase regulate a pool of phosphatidylinositol 4-phosphate that functions in the control of the actin cytoskeleton and vacuole morphology.Sac1脂质磷酸酶和Stt4磷脂酰肌醇4激酶调节着一组磷脂酰肌醇4磷酸,其在肌动蛋白细胞骨架和液泡形态的控制中发挥作用。
Mol Biol Cell. 2001 Aug;12(8):2396-411. doi: 10.1091/mbc.12.8.2396.
9
Essential role for the myotubularin-related phosphatase Ymr1p and the synaptojanin-like phosphatases Sjl2p and Sjl3p in regulation of phosphatidylinositol 3-phosphate in yeast.肌管素相关磷酸酶Ymr1p以及类突触素磷酸酶Sjl2p和Sjl3p在酵母中对磷脂酰肌醇3-磷酸调控的重要作用。
Mol Biol Cell. 2004 Aug;15(8):3567-79. doi: 10.1091/mbc.e04-03-0209. Epub 2004 May 28.
10
Atg18 regulates organelle morphology and Fab1 kinase activity independent of its membrane recruitment by phosphatidylinositol 3,5-bisphosphate.自噬相关蛋白18(Atg18)独立于磷脂酰肌醇3,5-二磷酸介导的膜募集作用,调控细胞器形态及Fab1激酶活性。
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PI(3,5)P2 asymmetry during mitosis is essential for asymmetric vacuolar inheritance.有丝分裂过程中 PI(3,5)P2 的不对称分布对于液泡的不对称遗传是必需的。
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Genome-wide CRISPR screens in spheroid culture reveal that the tumor suppressor LKB1 inhibits growth via the PIKFYVE lipid kinase.在球体培养物中的全基因组 CRISPR 筛选揭示,肿瘤抑制因子 LKB1 通过 PIKFYVE 脂质激酶抑制生长。
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The signalling lipid PI3,5P is essential for timely mitotic exit.信号脂质 PI3,5P 对于适时的有丝分裂退出是必不可少的。
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10
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本文引用的文献

1
The Vac14p-Fig4p complex acts independently of Vac7p and couples PI3,5P2 synthesis and turnover.Vac14p-Fig4p复合物独立于Vac7p发挥作用,并将磷脂酰肌醇-3,5-二磷酸(PI3,5P2)的合成与周转联系起来。
J Cell Biol. 2006 Feb 27;172(5):693-704. doi: 10.1083/jcb.200512105. Epub 2006 Feb 21.
2
mVps24p functions in EGF receptor sorting/trafficking from the early endosome.mVps24p在表皮生长因子受体从早期内体的分选/运输过程中发挥作用。
Exp Cell Res. 2005 Mar 10;304(1):265-73. doi: 10.1016/j.yexcr.2004.11.003. Epub 2004 Dec 1.
3
Subversion of phosphoinositide metabolism by intracellular bacterial pathogens.细胞内细菌病原体对磷酸肌醇代谢的破坏
Nat Cell Biol. 2004 Nov;6(11):1026-33. doi: 10.1038/ncb1104-1026.
4
Role for a novel signaling intermediate, phosphatidylinositol 5-phosphate, in insulin-regulated F-actin stress fiber breakdown and GLUT4 translocation.一种新型信号中间体磷脂酰肌醇5-磷酸在胰岛素调节的F-肌动蛋白应力纤维分解和葡萄糖转运蛋白4转位中的作用。
Endocrinology. 2004 Nov;145(11):4853-65. doi: 10.1210/en.2004-0489. Epub 2004 Jul 29.
5
Salmonella modulates vesicular traffic by altering phosphoinositide metabolism.沙门氏菌通过改变磷酸肌醇代谢来调节囊泡运输。
Science. 2004 Jun 18;304(5678):1805-7. doi: 10.1126/science.1098188.
6
Essential role for the myotubularin-related phosphatase Ymr1p and the synaptojanin-like phosphatases Sjl2p and Sjl3p in regulation of phosphatidylinositol 3-phosphate in yeast.肌管素相关磷酸酶Ymr1p以及类突触素磷酸酶Sjl2p和Sjl3p在酵母中对磷脂酰肌醇3-磷酸调控的重要作用。
Mol Biol Cell. 2004 Aug;15(8):3567-79. doi: 10.1091/mbc.e04-03-0209. Epub 2004 May 28.
7
Svp1p defines a family of phosphatidylinositol 3,5-bisphosphate effectors.Svp1p定义了一个磷脂酰肌醇3,5-二磷酸效应器家族。
EMBO J. 2004 May 5;23(9):1922-33. doi: 10.1038/sj.emboj.7600203. Epub 2004 Apr 22.
8
Osmotically induced cell swelling versus cell shrinking elicits specific changes in phospholipid signals in tobacco pollen tubes.渗透诱导的细胞肿胀与细胞收缩引发烟草花粉管中磷脂信号的特定变化。
Plant Physiol. 2004 Feb;134(2):813-23. doi: 10.1104/pp.103.029454. Epub 2004 Jan 22.
9
Myotubularin regulates the function of the late endosome through the gram domain-phosphatidylinositol 3,5-bisphosphate interaction.肌管素通过GRAM结构域与磷脂酰肌醇3,5-二磷酸的相互作用来调节晚期内体的功能。
J Biol Chem. 2004 Apr 2;279(14):13817-24. doi: 10.1074/jbc.M312294200. Epub 2004 Jan 12.
10
How versatile are inositol phosphate kinases?肌醇磷酸激酶的多功能性如何?
Biochem J. 2004 Jan 15;377(Pt 2):265-80. doi: 10.1042/BJ20031428.

磷酸肌醇5-磷酸酶Fig 4p对于应激诱导的磷脂酰肌醇3,5-二磷酸水平的急性升高及随后的下降均是必需的。

Phosphoinositide 5-phosphatase Fig 4p is required for both acute rise and subsequent fall in stress-induced phosphatidylinositol 3,5-bisphosphate levels.

作者信息

Duex Jason E, Nau Johnathan J, Kauffman Emily J, Weisman Lois S

机构信息

Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109-2216, USA.

出版信息

Eukaryot Cell. 2006 Apr;5(4):723-31. doi: 10.1128/EC.5.4.723-731.2006.

DOI:10.1128/EC.5.4.723-731.2006
PMID:16607019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1459661/
Abstract

Phosphoinositide lipids regulate complex events via the recruitment of proteins to a specialized region of the membrane at a specific time. Precise control of both the synthesis and turnover of phosphoinositide lipids is integral to membrane trafficking, signal transduction, and cytoskeletal rearrangements. Little is known about the acute regulation of the levels of these signaling lipids. When Saccharomyces cerevisiae cells are treated with hyperosmotic medium the levels of phosphatidylinositol 3,5-bisphosphate (PI3,5P(2)) increase 20-fold. Here we show that this 20-fold increase is rapid and occurs within 5 min. Surprisingly, these elevated levels are transient. Fifteen minutes following hyperosmotic shock they decrease at a rapid rate, even though the cells remain in hyperosmotic medium. In parallel with the rapid increase in the levels of PI3,5P(2), vacuole volume decreases rapidly. Furthermore, concomitant with a return to basal levels of PI3,5P(2) vacuole volume is restored. We show that Fig 4p, consistent with its proposed role as a PI3,5P(2) 5-phosphatase, is required in vivo for this rapid return to basal levels of PI3,5P(2). Surprisingly, we find that Fig 4p is also required for the hyperosmotic shock-induced increase in PI3,5P(2) levels. These findings demonstrate that following hyperosmotic shock, large, transient changes occur in the levels of PI3,5P(2) and further suggest that Fig 4p is important in regulating both the acute rise and subsequent fall in PI3,5P(2) levels.

摘要

磷酸肌醇脂质通过在特定时间将蛋白质招募到膜的特定区域来调节复杂事件。磷酸肌醇脂质合成与周转的精确控制对于膜运输、信号转导和细胞骨架重排至关重要。关于这些信号脂质水平的急性调节知之甚少。当酿酒酵母细胞用高渗培养基处理时,磷脂酰肌醇3,5-二磷酸(PI3,5P₂)的水平增加20倍。在这里我们表明,这种20倍的增加是迅速的,并且在5分钟内发生。令人惊讶的是,这些升高的水平是短暂的。高渗休克后15分钟,它们迅速下降,即使细胞仍处于高渗培养基中。与PI3,5P₂水平的迅速增加同时,液泡体积迅速减小。此外,随着PI3,5P₂恢复到基础水平,液泡体积也得以恢复。我们表明,Fig 4p与其作为PI3,5P₂ 5-磷酸酶的假定作用一致,在体内是PI3,5P₂迅速恢复到基础水平所必需的。令人惊讶的是,我们发现Fig 4p对于高渗休克诱导的PI3,5P₂水平升高也是必需的。这些发现表明,在高渗休克后,PI3,5P₂水平会发生大的、短暂的变化,并进一步表明Fig 4p在调节PI3,5P₂水平的急性升高和随后下降方面都很重要。