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本文引用的文献

1
A novel membrane fusion-mediated plant immunity against bacterial pathogens.一种新型的膜融合介导的植物对细菌病原体的免疫反应。
Genes Dev. 2009 Nov 1;23(21):2496-506. doi: 10.1101/gad.1825209. Epub 2009 Oct 15.
2
E3 ubiquitin ligases and plant innate immunity.E3泛素连接酶与植物先天免疫
J Exp Bot. 2009;60(4):1123-32. doi: 10.1093/jxb/erp059. Epub 2009 Mar 10.
3
Neuroprotective actions of PIKE-L by inhibition of SET proteolytic degradation by asparagine endopeptidase.PIKE-L通过抑制天冬酰胺内肽酶对SET的蛋白水解降解发挥神经保护作用。
Mol Cell. 2008 Mar 28;29(6):665-78. doi: 10.1016/j.molcel.2008.02.017.
4
What happened to plant caspases?植物中的半胱天冬酶怎么了?
J Exp Bot. 2008;59(3):491-9. doi: 10.1093/jxb/erm352. Epub 2008 Feb 13.
5
Arabidopsis VPS35, a retromer component, is required for vacuolar protein sorting and involved in plant growth and leaf senescence.拟南芥VPS35是一种回收受体复合物组分,参与液泡蛋白分选,并与植物生长和叶片衰老有关。
Plant Cell Physiol. 2008 Feb;49(2):142-56. doi: 10.1093/pcp/pcn006. Epub 2008 Jan 25.
6
Structure, function and regulation of plant proteasomes.植物蛋白酶体的结构、功能与调控
Biochimie. 2008 Feb;90(2):324-35. doi: 10.1016/j.biochi.2007.07.019. Epub 2007 Jul 31.
7
An asparaginyl endopeptidase mediates in vivo protein backbone cyclization.一种天冬酰胺内肽酶介导体内蛋白质主链环化。
J Biol Chem. 2007 Oct 5;282(40):29721-8. doi: 10.1074/jbc.M705185200. Epub 2007 Aug 13.
8
Ubiquitin, hormones and biotic stress in plants.植物中的泛素、激素与生物胁迫
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9
The plant immune system.植物免疫系统。
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10
AtVPS29, a putative component of a retromer complex, is required for the efficient sorting of seed storage proteins.拟逆转运蛋白复合体的一个假定组分AtVPS29是种子贮藏蛋白有效分选所必需的。
Plant Cell Physiol. 2006 Sep;47(9):1187-94. doi: 10.1093/pcp/pcj103. Epub 2006 Aug 22.

液泡在植物细胞死亡中的作用。

The role of vacuole in plant cell death.

机构信息

Department of Botany, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Cell Death Differ. 2011 Aug;18(8):1298-304. doi: 10.1038/cdd.2011.70. Epub 2011 Jun 3.

DOI:10.1038/cdd.2011.70
PMID:21637288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3172105/
Abstract

Almost all plant cells have large vacuoles that contain both hydrolytic enzymes and a variety of defense proteins. Plants use vacuoles and vacuolar contents for programmed cell death (PCD) in two different ways: for a destructive way and for a non-destructive way. Destruction is caused by vacuolar membrane collapse, followed by the release of vacuolar hydrolytic enzymes into the cytosol, resulting in rapid and direct cell death. The destructive way is effective in the digestion of viruses proliferating in the cytosol, in susceptible cell death induced by fungal toxins, and in developmental cell death to generate integuments (seed coats) and tracheary elements. On the other hand, the non-destructive way involves fusion of the vacuolar and the plasma membrane, which allows vacuolar defense proteins to be discharged into the extracellular space where the bacteria proliferate. Membrane fusion, which is normally suppressed, was triggered in a proteasome-dependent manner. Intriguingly, both ways use enzymes with caspase-like activity; the membrane-fusion system uses proteasome subunit PBA1 with caspase-3-like activity, and the vacuolar-collapse system uses vacuolar processing enzyme (VPE) with caspase-1-like activity. This review summarizes two different ways of vacuole-mediated PCD and discusses how plants use them to attack pathogens that invade unexpectedly.

摘要

几乎所有植物细胞都有大液泡,其中含有水解酶和各种防御蛋白。植物使用液泡和液泡内容物通过两种不同的方式实现程序性细胞死亡(PCD):一种是破坏性的方式,另一种是非破坏性的方式。破坏是由液泡膜崩溃引起的,随后液泡水解酶释放到细胞质中,导致细胞迅速直接死亡。这种破坏性的方式在消化细胞质中增殖的病毒、真菌毒素诱导的敏感细胞死亡以及为生成种皮和木质部元素而进行的发育性细胞死亡方面非常有效。另一方面,非破坏性方式涉及液泡和质膜的融合,这使得液泡防御蛋白可以被释放到细菌增殖的细胞外空间中。通常被抑制的膜融合是通过蛋白酶体依赖性方式触发的。有趣的是,这两种方式都使用具有半胱天冬酶样活性的酶;膜融合系统使用具有半胱天冬酶-3 样活性的蛋白酶体亚基 PBA1,而液泡崩溃系统使用具有半胱天冬酶-1 样活性的液泡加工酶(VPE)。本综述总结了液泡介导的 PCD 的两种不同方式,并讨论了植物如何利用它们来攻击意外入侵的病原体。