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过氧化物酶体和线粒体分裂的汇聚和发散机制。

Convergent and divergent mechanisms of peroxisomal and mitochondrial division.

机构信息

Department of Molecular Biology, School of Biological Sciences, University of California, San Diego, La Jolla, CA, USA.

出版信息

J Cell Biol. 2023 Sep 4;222(9). doi: 10.1083/jcb.202304076. Epub 2023 Aug 2.

DOI:10.1083/jcb.202304076
PMID:37530713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10397058/
Abstract

Organelle division and segregation are important in cellular homeostasis. Peroxisomes (POs) and mitochondria share a core division machinery and mechanism of membrane scission. The division of each organelle is interdependent not only on the other but also on other organelles, reflecting the dynamic communication between subcellular compartments, even as they coordinate the exchange of metabolites and signals. We highlight common and unique mechanisms involved in the fission of these organelles under the premise that much can be gleaned regarding the division of one organelle based on information available for the other.

摘要

细胞器的分裂和隔离对于细胞内稳态很重要。过氧化物酶体 (PO) 和线粒体共享核心分裂机制和膜分裂机制。每个细胞器的分裂不仅相互依赖,而且还依赖于其他细胞器,反映了亚细胞区室之间的动态通信,即使它们协调代谢物和信号的交换也是如此。我们在基于其他细胞器的可用信息可以了解一个细胞器的分裂的前提下,强调这些细胞器分裂所涉及的共同和独特的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/c2bff45c2cc7/JCB_202304076_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/85e27bcfab26/JCB_202304076_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/57f37931c2e0/JCB_202304076_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/57b34832540b/JCB_202304076_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/c2bff45c2cc7/JCB_202304076_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/85e27bcfab26/JCB_202304076_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/57f37931c2e0/JCB_202304076_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/57b34832540b/JCB_202304076_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3342/10397058/c2bff45c2cc7/JCB_202304076_Fig4.jpg

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2
The dynamin-related protein Vps1 and the peroxisomal membrane protein Pex27 function together during peroxisome fission.动力蛋白相关蛋白 Vps1 和过氧化物酶体膜蛋白 Pex27 在过氧化物酶体分裂过程中协同作用。
J Cell Sci. 2023 Mar 15;136(6). doi: 10.1242/jcs.246348. Epub 2023 Mar 24.
3
Genetic defects in peroxisome morphogenesis (Pex11β, dynamin-like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid-phospholipid metabolism.
过氧化物酶体形态发生的遗传缺陷(Pex11β、动力蛋白样蛋白1和核苷二磷酸激酶3)会影响二十二碳六烯酸磷脂代谢。
J Inherit Metab Dis. 2023 Mar;46(2):273-285. doi: 10.1002/jimd.12582. Epub 2022 Dec 23.
4
An ER phospholipid hydrolase drives ER-associated mitochondrial constriction for fission and fusion.内质网磷脂水解酶驱动内质网相关的线粒体收缩以促进裂变和融合。
Elife. 2022 Nov 30;11:e84279. doi: 10.7554/eLife.84279.
5
Structure-function analysis of the ER-peroxisome contact site protein Pex32.内质网-过氧化物酶体接触位点蛋白Pex32的结构-功能分析
Front Cell Dev Biol. 2022 Aug 9;10:957871. doi: 10.3389/fcell.2022.957871. eCollection 2022.
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HO Induces Calcium and ERMES Complex-Dependent Mitochondrial Constriction and Division as Well as Mitochondrial Outer Membrane Remodeling in .HO诱导钙和ERMES复合物依赖性的线粒体收缩与分裂以及线粒体的外膜重塑。
J Fungi (Basel). 2022 Aug 9;8(8):829. doi: 10.3390/jof8080829.
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Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders.分子视角下的过氧化物酶体动态平衡和过氧化物酶体生物发生障碍。
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