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A Novel Class of ER Membrane Proteins Regulates ER-Associated Endosome Fission.一类新型的内质网膜蛋白调控内质网相关内体分裂。
Cell. 2018 Sep 20;175(1):254-265.e14. doi: 10.1016/j.cell.2018.08.030. Epub 2018 Sep 13.
2
Receptor recognition by the peroxisomal AAA complex depends on the presence of the ubiquitin moiety and is mediated by Pex1p.过氧化物酶体 AAA 复合物通过 Pex1p 介导的泛素部分与受体的识别有关。
J Biol Chem. 2018 Oct 5;293(40):15458-15470. doi: 10.1074/jbc.RA118.003936. Epub 2018 Aug 10.
3
Structures, Functions, and Dynamics of ESCRT-III/Vps4 Membrane Remodeling and Fission Complexes.ESCRT-III/Vps4 膜重塑和裂变复合物的结构、功能和动力学。
Annu Rev Cell Dev Biol. 2018 Oct 6;34:85-109. doi: 10.1146/annurev-cellbio-100616-060600. Epub 2018 Aug 10.
4
Here, there, and everywhere: The importance of ER membrane contact sites.无处不在的内质网膜接触位点:重要性。
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Lipid droplet and peroxisome biogenesis occur at the same ER subdomains.脂滴和过氧化物酶体的生物发生发生在相同的内质网亚区。
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Seipin and the membrane-shaping protein Pex30 cooperate in organelle budding from the endoplasmic reticulum.Seipin 和膜成型蛋白 Pex30 合作在内质网从细胞器出芽。
Nat Commun. 2018 Jul 27;9(1):2939. doi: 10.1038/s41467-018-05278-2.
7
Pex19 is involved in importing dually targeted tail-anchored proteins to both mitochondria and peroxisomes.Pex19 参与将双重靶向的尾部锚定蛋白导入线粒体和过氧化物酶体。
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Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol.过氧化物酶体单泛素化 PEX5 与 AAA ATP 酶 PEX1 和 PEX6 相互作用,并在其易位到细胞质中时展开。
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9
Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact.系统绘制接触位点图谱揭示了质体-线粒体接触的连接蛋白和功能。
Nat Commun. 2018 May 2;9(1):1761. doi: 10.1038/s41467-018-03957-8.
10
Insights into the Role of the Peroxisomal Ubiquitination Machinery in Pex13p Degradation in the Yeast Hansenula polymorpha.对过氧化物酶体泛素化机制在酵母汉逊德巴利酵母 Pex13p 降解中作用的深入了解。
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过氧化物酶体的生物发生、膜接触位点和质量控制。

Peroxisome biogenesis, membrane contact sites, and quality control.

机构信息

Section of Molecular Biology, Division of Biological Sciences, University of California, San Diego, CA, USA.

Section of Molecular Biology, Division of Biological Sciences, University of California, San Diego, CA, USA

出版信息

EMBO Rep. 2019 Jan;20(1). doi: 10.15252/embr.201846864. Epub 2018 Dec 10.

DOI:10.15252/embr.201846864
PMID:30530632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6322382/
Abstract

Peroxisomes are conserved organelles of eukaryotic cells with important roles in cellular metabolism, human health, redox homeostasis, as well as intracellular metabolite transfer and signaling. We review here the current status of the different co-existing modes of biogenesis of peroxisomal membrane proteins demonstrating the fascinating adaptability in their targeting and sorting pathways. While earlier studies focused on peroxisomes as autonomous organelles, the necessity of the ER and potentially even mitochondria as sources of peroxisomal membrane proteins and lipids has come to light in recent years. Additionally, the intimate physical juxtaposition of peroxisomes with other organelles has transitioned from being viewed as random encounters to a growing appreciation of the expanding roles of such inter-organellar membrane contact sites in metabolic and regulatory functions. Peroxisomal quality control mechanisms have also come of age with a variety of mechanisms operating both during biogenesis and in the cellular response to environmental cues.

摘要

过氧化物酶体是真核细胞中保守的细胞器,在细胞代谢、人类健康、氧化还原稳态以及细胞内代谢物转移和信号转导中具有重要作用。我们在这里回顾了过氧化物酶体膜蛋白不同共存生物发生模式的最新研究进展,这些模式展示了其在靶向和分拣途径中的惊人适应性。虽然早期的研究集中在过氧化物酶体作为自主细胞器,但近年来,内质网甚至线粒体作为过氧化物酶体膜蛋白和脂质来源的必要性已经显现出来。此外,过氧化物体与其他细胞器的紧密物理毗邻已经从随机相遇转变为越来越多地认识到这种细胞器间膜接触位点在代谢和调节功能中的扩展作用。过氧化物酶体的质量控制机制也随着各种机制在生物发生过程中和细胞对环境信号的反应中发挥作用而不断发展。