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本文引用的文献

1
A matrix protein silences transposons and repeats through interaction with retinoblastoma-associated proteins.基质蛋白通过与视网膜母细胞瘤相关蛋白的相互作用来沉默转座子和重复序列。
Curr Biol. 2013 Feb 18;23(4):345-50. doi: 10.1016/j.cub.2013.01.030. Epub 2013 Feb 7.
2
Genome-wide analysis of DNA methylation and gene expression changes in two Arabidopsis ecotypes and their reciprocal hybrids.全基因组分析两个拟南芥生态型及其正反交杂种中 DNA 甲基化和基因表达的变化。
Plant Cell. 2012 Mar;24(3):875-92. doi: 10.1105/tpc.111.094870. Epub 2012 Mar 20.
3
Regulation of the floral repressor gene FLC: the complexity of transcription in a chromatin context.调控花抑制基因 FLC:染色质背景下转录的复杂性。
Curr Opin Plant Biol. 2011 Feb;14(1):38-44. doi: 10.1016/j.pbi.2010.08.015. Epub 2010 Sep 29.
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Differentiation of epigenetic modifications between transposons and genes.转座子与基因之间的表观遗传修饰的分化。
Curr Opin Plant Biol. 2011 Feb;14(1):81-7. doi: 10.1016/j.pbi.2010.08.017. Epub 2010 Sep 23.
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Seasonal and developmental timing of flowering.开花的季节性和发育时间。
Plant J. 2010 Mar;61(6):1001-13. doi: 10.1111/j.1365-313X.2010.04148.x.
6
AGAMOUS controls GIANT KILLER, a multifunctional chromatin modifier in reproductive organ patterning and differentiation.AGAMOUS 控制 GIANT KILLER,这是一种多功能染色质修饰因子,在生殖器官的形态发生和分化中起作用。
PLoS Biol. 2009 Nov;7(11):e1000251. doi: 10.1371/journal.pbio.1000251. Epub 2009 Nov 24.
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8
Repression of FLOWERING LOCUS C and FLOWERING LOCUS T by the Arabidopsis Polycomb repressive complex 2 components.拟南芥多梳抑制复合体2组分对开花位点C和开花位点T的抑制作用
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Noncoding RNAs and gene silencing.非编码RNA与基因沉默
Cell. 2007 Feb 23;128(4):763-76. doi: 10.1016/j.cell.2007.02.016.

AT 钩/PPC 结构域蛋白 TEK 负调控包括 MAF4 和 MAF5 在内的花发育抑制子。

The AT-hook/PPC domain protein TEK negatively regulates floral repressors including MAF4 and MAF5.

机构信息

Temasek Life Sciences Laboratory (TLL); 1 Research Link; National University of Singapore; Singapore.

出版信息

Plant Signal Behav. 2013 Aug;8(8). doi: 10.4161/psb.25006. Epub 2013 May 15.

DOI:10.4161/psb.25006
PMID:23733063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3999084/
Abstract

Epigenetic regulations of transposable elements (TEs) and TE-like repeat sequences help to protect genomic integrity and control various developmental processes, including flowering time. This complex action of gene silencing requires the coordination of many key players including DNA methylases, histone deacetylases and histone methyltranferases. We have recently reported that an AT-hook DNA binding protein, TRANSPOSABLE ELEMENT SILENCING VIA AT-HOOK (TEK), participates in silencing TEs and TE-like sequence containing genes, such as Ler FLOWERING LOCUS C (FLC) and FWA. TEK knockdown in amiTEK plants causes increased histone acetylation, reduced H3K9me2 and DNA hypomethylation in the target loci, which ultimately leads to the upregulation of FLC and FWA as well as TE reactivation. In this report, we show that, besides FLC, other FLC-like genes MADS AFFECTING FLOWERING 4 (MAF4) and MAF5 are also upregulated in amiTEK. Here we discuss the role of the nuclear matrix protein TEK in the maintenance of genome integrity and in the control of flowering.

摘要

转座元件 (TEs) 和类 TE 重复序列的表观遗传调控有助于保护基因组完整性,并控制各种发育过程,包括开花时间。这种基因沉默的复杂作用需要许多关键因子的协调,包括 DNA 甲基转移酶、组蛋白去乙酰化酶和组蛋白甲基转移酶。我们最近报道,一个 AT 钩 DNA 结合蛋白,通过 AT 钩转座元件沉默 (TEK),参与沉默 TEs 和含有类 TE 序列的基因,如 Ler 开花时间基因 C (FLC) 和 FWA。amiTEK 植物中的 TEK 敲低导致靶基因中组蛋白乙酰化增加、H3K9me2 减少和 DNA 低甲基化,最终导致 FLC 和 FWA 的上调以及 TE 的重新激活。在本报告中,我们表明,除了 FLC 之外,amiTEK 中还上调了其他 FLC 样基因 MADS 影响开花 4 (MAF4) 和 MAF5。在这里,我们讨论了核基质蛋白 TEK 在维持基因组完整性和控制开花时间方面的作用。