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本文引用的文献

1
Arabidopsis ULTRAVIOLET-B-INSENSITIVE4 maintains cell division activity by temporal inhibition of the anaphase-promoting complex/cyclosome.拟南芥 UV 不敏感 4 蛋白通过暂时抑制后期促进复合物/周期蛋白来维持细胞分裂活性。
Plant Cell. 2011 Dec;23(12):4394-410. doi: 10.1105/tpc.111.091793. Epub 2011 Dec 13.
2
GIGAS CELL1, a novel negative regulator of the anaphase-promoting complex/cyclosome, is required for proper mitotic progression and cell fate determination in Arabidopsis.GIGAS CELL1,一种新型的有丝分裂促进复合物/周期蛋白体的负调控因子,对于拟南芥中正确的有丝分裂进程和细胞命运决定是必需的。
Plant Cell. 2011 Dec;23(12):4382-93. doi: 10.1105/tpc.111.092049. Epub 2011 Dec 13.
3
CDKB2 is involved in mitosis and DNA damage response in rice.CDKB2 参与水稻的有丝分裂和 DNA 损伤反应。
Plant J. 2012 Mar;69(6):967-77. doi: 10.1111/j.1365-313X.2011.04847.x. Epub 2011 Dec 15.
4
Molecular control and function of endoreplication in development and physiology.在发育和生理学中,内复制的分子控制和功能。
Trends Plant Sci. 2011 Nov;16(11):624-34. doi: 10.1016/j.tplants.2011.07.001. Epub 2011 Sep 1.
5
Mutations in MYB3R1 and MYB3R4 cause pleiotropic developmental defects and preferential down-regulation of multiple G2/M-specific genes in Arabidopsis.MYB3R1 和 MYB3R4 中的突变导致拟南芥多效性发育缺陷和多个 G2/M 特异性基因的优先下调。
Plant Physiol. 2011 Oct;157(2):706-17. doi: 10.1104/pp.111.180836. Epub 2011 Aug 23.
6
Structure, function and mechanism of the anaphase promoting complex (APC/C).有丝分裂后期促进复合物(APC/C)的结构、功能和机制。
Q Rev Biophys. 2011 May;44(2):153-90. doi: 10.1017/S0033583510000259. Epub 2010 Nov 22.
7
Endoreplication: polyploidy with purpose.核内复制:有特定目的的多倍体现象。
Genes Dev. 2009 Nov 1;23(21):2461-77. doi: 10.1101/gad.1829209.
8
Regulation of APC/C activators in mitosis and meiosis.有丝分裂和减数分裂中后期促进复合物/细胞周期体(APC/C)激活因子的调控
Annu Rev Cell Dev Biol. 2008;24:475-99. doi: 10.1146/annurev.cellbio.041408.115949.
9
R1R2R3-Myb proteins positively regulate cytokinesis through activation of KNOLLE transcription in Arabidopsis thaliana.在拟南芥中,R1R2R3-Myb蛋白通过激活KNOLLE转录正向调控胞质分裂。
Development. 2007 Mar;134(6):1101-10. doi: 10.1242/dev.02801. Epub 2007 Feb 7.
10
A mutation in the uvi4 gene promotes progression of endo-reduplication and confers increased tolerance towards ultraviolet B light.uvi4基因的突变促进了核内复制的进程,并赋予对紫外线B更强的耐受性。
Plant J. 2006 Apr;46(2):317-26. doi: 10.1111/j.1365-313X.2006.02696.x.

GIG1 和 UVI4 在拟南芥基因组复制中的作用。

Roles of GIG1 and UVI4 in genome duplication in Arabidopsis thaliana.

机构信息

Graduate School of Bioagricultural Sciences; Nagoya University; Chikusa, Nagoya, Japan.

出版信息

Plant Signal Behav. 2012 Sep 1;7(9):1079-81. doi: 10.4161/psb.21133. Epub 2012 Aug 17.

DOI:10.4161/psb.21133
PMID:22899078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3489631/
Abstract

Endomitosis and endoreplication are atypical modes of cell cycle that results in genome duplication in single nucleus. Because the cell size of given cell type is generally proportional to the nuclear DNA content, endoreplication and endomitosis are effective strategy of cell growth, which are widespread in multicellular organisms, especially those in plant kingdom. We found that these processes might be differently regulated by GIGAS CELL1 (GIG1) and its paralog UV-INSENSITIVE4 (UVI4) in Arabidopsis thaliana. GIG1 and UVI4 may negatively regulate activities of anaphase-promoting complex or cyclosome (APC/C) ubiquitin ligase that acts as an important mitotic regulator. The gig1 mutation induced ectopic occurrence of endomitosis during somatic cell division, while it has been reported that uvi4 mutation resulted in premature occurrence of endoreplication during organ development. Overexpression of GIG1 and UVI4 dramatically increased the amount of mitotic cyclin, CYCB1;1, a well-known substrate of APC/C. Ectopic endomitosis in gig1 was enhanced by mutation in CYCB2;2 and suppressed by downregulation of APC10 encoding a core subunit of APC/C. Overexpression of CDC20.1, an activator protein of APC/C, further promoted the ectopic endomitosis in gig1. These findings suggest that endomitosis and endoreplication are regulated by similar molecular mechanisms, in which two related proteins, GIG1 and UVI4, may inhibit APC/C in different ways.

摘要

核内有丝分裂和核内复制是细胞周期的非典型模式,导致单个核内的基因组复制。由于给定细胞类型的细胞大小通常与核 DNA 含量成正比,因此核内复制和核内有丝分裂是细胞生长的有效策略,在多细胞生物中广泛存在,尤其是在植物界。我们发现这些过程可能在拟南芥中由 GIGAS CELL1(GIG1)及其同源物 UV-INSENSITIVE4(UVI4)以不同的方式调节。GIG1 和 UVI4 可能负调节后期促进复合物或细胞周期蛋白(APC/C)泛素连接酶的活性,APC/C 作为重要的有丝分裂调节剂。gig1 突变诱导体细胞分裂过程中核内有丝分裂的异位发生,而 uvi4 突变已被报道导致器官发育过程中核内复制的过早发生。GIG1 和 UVI4 的过表达显著增加了有丝分裂周期蛋白 CYCB1;1 的量,CYCB1;1 是 APC/C 的一个重要底物。gig1 中的异位核内有丝分裂通过突变 CYCB2;2 增强,并通过下调 APC/C 的核心亚基 APC10 抑制。APC/C 的激活蛋白 CDC20.1 的过表达进一步促进了 gig1 中的异位核内有丝分裂。这些发现表明核内有丝分裂和核内复制受相似的分子机制调节,其中两个相关蛋白 GIG1 和 UVI4 可能以不同的方式抑制 APC/C。