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本文引用的文献

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A core subunit of Polycomb repressive complex 1 is broadly conserved in function but not primary sequence.多梳抑制复合物 1 的核心亚基在功能上广泛保守,但在一级序列上没有保守性。
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EMF1 and PRC2 cooperate to repress key regulators of Arabidopsis development.EMF1 和 PRC2 合作抑制拟南芥发育的关键调控因子。
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Antagonistic roles of SEPALLATA3, FT and FLC genes as targets of the polycomb group gene CURLY LEAF.SEPALLATA3、FT 和 FLC 基因作为多梳组基因 CURLY LEAF 的靶标拮抗作用。
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SWI2/SNF2 chromatin remodeling ATPases overcome polycomb repression and control floral organ identity with the LEAFY and SEPALLATA3 transcription factors.SWI2/SNF2 染色质重塑 ATP 酶克服多梳抑制并与 LEAFY 和 SEPALLATA3 转录因子一起控制花器官的身份。
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Polycomb group complexes mediate developmental transitions in plants.多梳蛋白复合体介导植物的发育转变。
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Tissue-specific expression of FLOWERING LOCUS T in Arabidopsis is maintained independently of polycomb group protein repression.拟南芥 FLOWERING LOCUS T 的组织特异性表达独立于多梳蛋白抑制。
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Histone methylation by PRC2 is inhibited by active chromatin marks.PRC2 介导的组蛋白甲基化受活性染色质标记抑制。
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LEAFY target genes reveal floral regulatory logic, cis motifs, and a link to biotic stimulus response.叶性靶基因揭示花发育调控逻辑、顺式作用元件及其与生物刺激响应的联系。
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Keeping cell identity in Arabidopsis requires PRC1 RING-finger homologs that catalyze H2A monoubiquitination.维持拟南芥细胞的身份需要 PRC1 RING 指蛋白同源物,它们催化 H2A 单泛素化。
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胚胎花 1 和超花瓣 1 对拟南芥发育和应激反应具有拮抗作用。

EMBRYONIC FLOWER1 and ULTRAPETALA1 Act Antagonistically on Arabidopsis Development and Stress Response.

机构信息

Department of Plant and Microbial Biology, University of California, Berkeley, California 94720, USA.

出版信息

Plant Physiol. 2013 Jun;162(2):812-30. doi: 10.1104/pp.112.213223. Epub 2013 Apr 30.

DOI:10.1104/pp.112.213223
PMID:23632855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3668072/
Abstract

Epigenetic regulation of gene expression is of fundamental importance for eukaryotic development. EMBRYONIC FLOWER1 (EMF1) is a plant-specific gene that participates in Polycomb group-mediated transcriptional repression of target genes such as the flower MADS box genes AGAMOUS, APETALA3, and PISTILLATA. Here, we investigated the molecular mechanism underlying the curly leaf and early flowering phenotypes caused by reducing EMF1 activity in the leaf primordia of LFYasEMF1 transgenic plants and propose a combined effect of multiple flower MADS box gene activities on these phenotypes. ULTRAPETALA1 (ULT1) functions as a trithorax group factor that counteracts Polycomb group action in Arabidopsis (Arabidopsis thaliana). Removing ULT1 activity rescues both the abnormal developmental phenotypes and most of the misregulated gene expression of LFYasEMF1 plants. Reducing EMF1 activity increases salt tolerance, an effect that is diminished by introducing the ult1-3 mutation into the LFYasEMF1 background. EMF1 is required for trimethylating lysine-27 on histone 3 (H3K27me3), and ULT1 associates with ARABIDOPSIS TRITHORAX1 (ATX1) for trimethylating lysine-3 on histone 4 (H3K4me3) at flower MADS box gene loci. Reducing EMF1 activity decreases H3K27me3 marks and increases H3K4me3 marks on target gene loci. Removing ULT1 activity has the opposite effect on the two histone marks. Removing both gene activities restores the active and repressive marks to near wild-type levels. Thus, ULT1 acts as an antirepressor that counteracts EMF1 action through modulation of histone marks on target genes. Our analysis indicates that, instead of acting as off and on switches, EMF1 and ULT1 mediate histone mark deposition and modulate transcriptional activities of the target genes.

摘要

表观遗传调控基因表达对于真核生物的发育至关重要。EMBRYONIC FLOWER1(EMF1)是一种植物特异性基因,参与多梳组蛋白介导的靶基因转录抑制,如花 MADS 盒基因 AGAMOUS、APETALA3 和 PISTILLATA。在这里,我们研究了减少 LFYasEMF1 转基因植物叶原基中 EMF1 活性引起的卷曲叶和早花表型的分子机制,并提出了多个花 MADS 盒基因活性对这些表型的综合影响。ULTRAPETALA1(ULT1)作为一个转录激活因子,在拟南芥中对抗多梳组蛋白的作用。去除 ULT1 活性可挽救 LFYasEMF1 植物的异常发育表型和大部分失调基因的表达。减少 EMF1 活性可提高耐盐性,而将 ult1-3 突变引入 LFYasEMF1 背景中则会降低这种效应。EMF1 是赖氨酸-27 三甲基化(H3K27me3)所必需的,ULT1 与 ARABIDOPSIS TRITHORAX1(ATX1)结合,在花 MADS 盒基因座上对赖氨酸-3 进行三甲基化(H3K4me3)。减少 EMF1 活性会降低靶基因座上的 H3K27me3 标记,并增加 H3K4me3 标记。去除 ULT1 活性对这两种组蛋白标记有相反的影响。去除两种基因活性可使活性和抑制性标记恢复到接近野生型水平。因此,ULT1 作为一种反抑制因子,通过调节靶基因上的组蛋白标记来拮抗 EMF1 的作用。我们的分析表明,EMF1 和 ULT1 不是作为开和关开关,而是通过调节靶基因的组蛋白标记沉积和调节转录活性来介导。