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本文引用的文献

1
Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion.Mgm1 亚型的共组装需要心磷脂并介导线粒体内膜融合。
J Cell Biol. 2009 Sep 21;186(6):793-803. doi: 10.1083/jcb.200906098. Epub 2009 Sep 14.
2
The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice.与发动蛋白相关的GTP酶Drp1是小鼠胚胎发育和大脑发育所必需的。
J Cell Biol. 2009 Sep 21;186(6):805-16. doi: 10.1083/jcb.200903065. Epub 2009 Sep 14.
3
The BCL-2-like protein CED-9 of C. elegans promotes FZO-1/Mfn1,2- and EAT-3/Opa1-dependent mitochondrial fusion.秀丽隐杆线虫的BCL-2样蛋白CED-9促进FZO-1/Mfn1、2和EAT-3/Opa1依赖性的线粒体融合。
J Cell Biol. 2009 Aug 24;186(4):525-40. doi: 10.1083/jcb.200905070.
4
Origins. On the origin of eukaryotes.起源。关于真核生物的起源。
Science. 2009 Aug 7;325(5941):666-8. doi: 10.1126/science.325_666.
5
A hyperfused mitochondrial state achieved at G1-S regulates cyclin E buildup and entry into S phase.在G1-S期达到的线粒体高度融合状态调节细胞周期蛋白E的积累并进入S期。
Proc Natl Acad Sci U S A. 2009 Jul 21;106(29):11960-5. doi: 10.1073/pnas.0904875106. Epub 2009 Jul 15.
6
Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.线粒体分裂因子Drp1对小鼠的胚胎发育和突触形成至关重要。
Nat Cell Biol. 2009 Aug;11(8):958-66. doi: 10.1038/ncb1907. Epub 2009 Jul 5.
7
Mechanisms of endocytosis.内吞作用的机制。
Annu Rev Biochem. 2009;78:857-902. doi: 10.1146/annurev.biochem.78.081307.110540.
8
Bcl-x L increases mitochondrial fission, fusion, and biomass in neurons.Bcl-x L增加神经元中的线粒体裂变、融合及生物量。
J Cell Biol. 2009 Mar 9;184(5):707-19. doi: 10.1083/jcb.200809060. Epub 2009 Mar 2.
9
The molecular mechanism and cellular functions of mitochondrial division.线粒体分裂的分子机制和细胞功能。
Biochim Biophys Acta. 2009 Dec;1792(12):1138-44. doi: 10.1016/j.bbadis.2008.11.011. Epub 2008 Dec 3.
10
Arabidopsis ELONGATED MITOCHONDRIA1 is required for localization of DYNAMIN-RELATED PROTEIN3A to mitochondrial fission sites.拟南芥的ELONGATED MITOCHONDRIA1是动力相关蛋白3A定位于线粒体分裂位点所必需的。
Plant Cell. 2008 Jun;20(6):1555-66. doi: 10.1105/tpc.108.058578. Epub 2008 Jun 17.

线粒体的分裂与融合。

Mitochondrial fission and fusion.

机构信息

National Heart, Lung and Blood Institute, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

出版信息

Essays Biochem. 2010;47:85-98. doi: 10.1042/bse0470085.

DOI:10.1042/bse0470085
PMID:20533902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4762097/
Abstract

Mitochondria are highly dynamic cellular organelles, with the ability to change size, shape and position over the course of a few seconds. Many of these changes are related to the ability of mitochondria to undergo the highly co-ordinated processes of fission (division of a single organelle into two or more independent structures) or fusion (the opposing reaction). These actions occur simultaneously and continuously in many cell types, and the balance between them regulates the overall morphology of mitochondria within any given cell. Fission and fusion are active processes which require many specialized proteins, including mechanical enzymes that physically alter mitochondrial membranes, and adaptor proteins that regulate the interaction of these mechanical proteins with organelles. Although not fully understood, alterations in mitochondrial morphology appear to be involved in several activities that are crucial to the health of cells. In the present chapter we discuss the mechanisms behind mitochondrial fission and fusion, and discuss the implications of changes in organelle morphology during the life of a cell.

摘要

线粒体是高度动态的细胞细胞器,能够在几秒钟内改变大小、形状和位置。许多这些变化与线粒体能够进行高度协调的分裂(将单个细胞器分裂成两个或更多个独立结构)或融合(相反的反应)过程有关。这些动作在许多细胞类型中同时且连续地发生,它们之间的平衡调节了给定细胞内线粒体的整体形态。分裂和融合是需要许多专门蛋白质的活跃过程,包括物理改变线粒体膜的机械酶,以及调节这些机械蛋白与细胞器相互作用的衔接蛋白。尽管尚未完全理解,但线粒体形态的改变似乎与细胞健康至关重要的几种活动有关。在本章中,我们讨论了线粒体分裂和融合背后的机制,并讨论了细胞器形态在细胞生命过程中的变化的影响。

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