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本文引用的文献

1
Mutations in the Type II protein arginine methyltransferase AtPRMT5 result in pleiotropic developmental defects in Arabidopsis.II型蛋白质精氨酸甲基转移酶AtPRMT5中的突变导致拟南芥出现多效性发育缺陷。
Plant Physiol. 2007 Aug;144(4):1913-23. doi: 10.1104/pp.107.099531. Epub 2007 Jun 15.
2
Spinophilin/neurabin reciprocally regulate signaling intensity by G protein-coupled receptors.亲环蛋白/神经肌动蛋白通过G蛋白偶联受体相互调节信号强度。
EMBO J. 2007 Jun 6;26(11):2768-76. doi: 10.1038/sj.emboj.7601701. Epub 2007 Apr 26.
3
The PHD finger protein VRN5 functions in the epigenetic silencing of Arabidopsis FLC.PHD指蛋白VRN5在拟南芥FLC的表观遗传沉默中发挥作用。
Curr Biol. 2007 Jan 9;17(1):73-8. doi: 10.1016/j.cub.2006.11.052. Epub 2006 Dec 14.
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A PHD finger protein involved in both the vernalization and photoperiod pathways in Arabidopsis.一种参与拟南芥春化和光周期途径的博士指蛋白。
Genes Dev. 2006 Dec 1;20(23):3244-8. doi: 10.1101/gad.1493306. Epub 2006 Nov 17.
5
The protein arginine methyltransferase Prmt5 is required for myogenesis because it facilitates ATP-dependent chromatin remodeling.蛋白质精氨酸甲基转移酶Prmt5是肌生成所必需的,因为它促进依赖ATP的染色质重塑。
Mol Cell Biol. 2007 Jan;27(1):384-94. doi: 10.1128/MCB.01528-06. Epub 2006 Oct 16.
6
The Arabidopsis thaliana vernalization response requires a polycomb-like protein complex that also includes VERNALIZATION INSENSITIVE 3.拟南芥的春化反应需要一种类似多梳蛋白的复合体,该复合体还包括春化不敏感3蛋白。
Proc Natl Acad Sci U S A. 2006 Sep 26;103(39):14631-6. doi: 10.1073/pnas.0606385103. Epub 2006 Sep 18.
7
Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells.Blimp1与Prmt5相互作用,并在小鼠生殖细胞中指导组蛋白精氨酸甲基化。
Nat Cell Biol. 2006 Jun;8(6):623-30. doi: 10.1038/ncb1413. Epub 2006 May 14.
8
Epigenetic maintenance of the vernalized state in Arabidopsis thaliana requires LIKE HETEROCHROMATIN PROTEIN 1.拟南芥春化状态的表观遗传维持需要类异染色质蛋白1。
Nat Genet. 2006 Jun;38(6):706-10. doi: 10.1038/ng1795. Epub 2006 May 7.
9
LHP1, the Arabidopsis homologue of HETEROCHROMATIN PROTEIN1, is required for epigenetic silencing of FLC.LHP1是拟南芥中与异染色质蛋白1同源的蛋白,它是FLC表观遗传沉默所必需的。
Proc Natl Acad Sci U S A. 2006 Mar 28;103(13):5012-7. doi: 10.1073/pnas.0507427103. Epub 2006 Mar 20.
10
FRIGIDA-ESSENTIAL 1 interacts genetically with FRIGIDA and FRIGIDA-LIKE 1 to promote the winter-annual habit of Arabidopsis thaliana.FRIGIDA-ESSENTIAL 1与FRIGIDA和FRIGIDA-LIKE 1发生遗传相互作用,以促进拟南芥的冬性一年生习性。
Development. 2005 Dec;132(24):5471-8. doi: 10.1242/dev.02170. Epub 2005 Nov 16.

在冬性一年生拟南芥中,组蛋白精氨酸甲基化是春化诱导的FLC表观遗传沉默所必需的。

Histone arginine methylation is required for vernalization-induced epigenetic silencing of FLC in winter-annual Arabidopsis thaliana.

作者信息

Schmitz Robert J, Sung Sibum, Amasino Richard M

机构信息

Laboratory of Genetics and Department of Biochemistry, University of Wisconsin, Madison, WI 53706, USA.

出版信息

Proc Natl Acad Sci U S A. 2008 Jan 15;105(2):411-6. doi: 10.1073/pnas.0710423104. Epub 2008 Jan 4.

DOI:10.1073/pnas.0710423104
PMID:18178621
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2206549/
Abstract

Certain plant varieties typically require prolonged exposure to the cold of winter to become competent to flower rapidly in the spring. This process is known as vernalization. In Arabidopsis thaliana, vernalization renders plants competent to flower by epigenetically silencing the strong floral repressor FLOWERING LOCUS C (FLC). As a result of vernalization, levels of lysine-9 and lysine-27 trimethylation on histone 3, modifications that are characteristic of facultative heterochromatin in plants, increase at FLC chromatin. We have identified a mutant, protein arginine methyltransferase 5 (atprmt5), that fails to flower rapidly after vernalization treatment. AtPRMT5 encodes a type II protein arginine methyltransferase (PRMT) that, in winter-annual strains, is required for epigenetic silencing of FLC and for the vernalization-mediated histone modifications characteristic of the vernalized state. Furthermore, the levels of arginine methylation of FLC chromatin increase after vernalization. Therefore, arginine methylation of FLC chromatin is part of the histone code that is required for mitotic stability of the vernalized state.

摘要

某些植物品种通常需要长时间暴露在冬季的寒冷环境中,才能在春季迅速具备开花能力。这个过程被称为春化作用。在拟南芥中,春化作用通过对强大的开花抑制因子开花位点C(FLC)进行表观遗传沉默,使植物具备开花能力。春化作用的结果是,组蛋白3上赖氨酸-9和赖氨酸-27三甲基化水平增加,这些修饰是植物兼性异染色质的特征,在FLC染色质上出现。我们鉴定出了一个突变体,即蛋白质精氨酸甲基转移酶5(AtPRMT5),它在春化处理后不能迅速开花。AtPRMT5编码一种II型蛋白质精氨酸甲基转移酶(PRMT),在冬性一年生品系中,它是FLC表观遗传沉默以及春化介导的春化状态特征性组蛋白修饰所必需的。此外,春化作用后FLC染色质的精氨酸甲基化水平增加。因此,FLC染色质的精氨酸甲基化是春化状态有丝分裂稳定性所需组蛋白密码的一部分。