Our FABulous VACation: a decade of phosphatidylinositol 3,5-bisphosphate.

Stephen K Dove, Zoë E Johnson
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引用次数: 15

Abstract

PtdIns(3,5)P2 was discovered about a decade ago and much of the machinery that makes, degrades and senses it has been uncovered. Despite this, we still lack a complete understanding of how the pieces fit together but some patterns are beginning to emerge. Molecular functions for PtdIns(3,5)P2 are also elusive, but the identification of effectors offers a way into some of these processes. An examination of the defects associated with loss of synthesis of PtdIns(3,5)P2 in lower and higher eukaryotes begins to suggest a unifying theme; this lipid regulates membrane retrieval via retrograde trafficking from distal compartments to organelles that are more proximal in the endocytic/lysosomal system. Another unifying theme is stress signalling to organelles, possibly both to change their morphology in response to external insults and to maintain the lumenal pH or membrane potential of organelles. The next few years seem likely to uncover details of the molecular mechanisms underlying the biology of this fascinating lipid. This review also highlights some areas where further research is needed.

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我们的美妙假期:磷脂酰肌醇3,5-二磷酸的十年。
PtdIns(3,5)P2大约在十年前被发现,许多制造、降解和感知它的机制已经被发现。尽管如此,我们仍然缺乏对各个部分如何组合在一起的完整理解,但一些模式已经开始出现。PtdIns(3,5)P2的分子功能也是难以捉摸的,但效应物的鉴定为研究这些过程提供了一条途径。在低等和高等真核生物中,与PtdIns(3,5)P2合成损失相关的缺陷的检查开始提出一个统一的主题;这种脂质通过内吞/溶酶体系统中从远端室向更近端的细胞器的逆行运输调节膜回收。另一个统一的主题是向细胞器发出应激信号,可能既改变其形态以响应外部损伤,又维持细胞器的管腔pH或膜电位。接下来的几年似乎有可能揭示这种令人着迷的脂质生物学背后的分子机制的细节。这篇综述还强调了一些需要进一步研究的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Pleckstrin homology (PH) domains and phosphoinositides. Evolutionarily conserved structural and functional roles of the FYVE domain. The role of the phosphoinositides at the Golgi complex. PtdIns5P: a little phosphoinositide with big functions? Our FABulous VACation: a decade of phosphatidylinositol 3,5-bisphosphate.
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