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拟南芥中春化作用导致基因抑制的机制。

Mechanisms of gene repression by vernalization in Arabidopsis.

作者信息

Sheldon Candice C, Finnegan E Jean, Peacock W James, Dennis Elizabeth S

机构信息

Commonwealth Scientific and Industrial Research Organization, Plant Industry, ACT, Australia.

出版信息

Plant J. 2009 Aug;59(3):488-98. doi: 10.1111/j.1365-313X.2009.03883.x. Epub 2009 Apr 2.

Abstract

FLOWERING LOCUS C (FLC) is a major regulator of flowering time in Arabidopsis. Repression of FLC occurs in response to prolonged cold exposure (vernalization) and is associated with an enrichment of the repressive histone modification trimethylated H3 lysine 27 (H3K27me3) and a depletion of the active histone modification H3K4me3 at FLC chromatin. In two cases genes adjacent to FLC are also repressed by vernalization. NEOMYCIN PHOSPHOTRANSFERASE II (NPTII) adjacent to an FLC transgene is repressed by vernalization, and this is associated with an increase in H3K27me3, demonstrating that the epigenetic repression of FLC can confer a repressed epigenetic state to an adjacent transcription unit. The second case involves the two genes adjacent to the endogenous FLC gene, UPSTREAM OF FLC (UFC) and DOWNSTREAM OF FLC (DFC). Both genes are repressed by vernalization (Finnegan et al., 2004), but they require neither cis-acting nor trans-acting factors derived from the FLC gene nor the VERNALIZATION2 (VRN2) complex which trimethylates H3K27. This demonstrates that there are two different mechanisms of gene repression by vernalization. We further show that repression and H3K27 trimethylation of FLC still occurs in mutants of the VRN2 complex. In contrast, the VRN2 complex is essential for repression and H3K27 trimethylation of the FLC-related MADS AFFECTING FLOWERING (MAF) genes by vernalization. This suggest that other proteins are able to repress FLC, but not MAF, gene expression.

摘要

开花位点C(FLC)是拟南芥开花时间的主要调节因子。FLC的抑制发生在长时间冷暴露(春化作用)后,并且与FLC染色质上抑制性组蛋白修饰三甲基化H3赖氨酸27(H3K27me3)的富集以及活性组蛋白修饰H3K4me3的减少有关。在两种情况下,与FLC相邻的基因也会被春化作用抑制。与FLC转基因相邻的新霉素磷酸转移酶II(NPTII)被春化作用抑制,这与H3K27me3的增加有关,表明FLC的表观遗传抑制可以赋予相邻转录单元一个抑制性的表观遗传状态。第二个例子涉及与内源性FLC基因相邻的两个基因,FLC上游(UFC)和FLC下游(DFC)。这两个基因都被春化作用抑制(芬尼根等人,2004年),但它们既不需要来自FLC基因的顺式作用因子也不需要反式作用因子,也不需要使H3K27三甲基化的春化作用2(VRN2)复合体。这表明存在两种不同的春化作用基因抑制机制。我们进一步表明,在VRN2复合体的突变体中,FLC的抑制和H3K27三甲基化仍然会发生。相比之下,VRN2复合体对于春化作用抑制FLC相关的影响开花的MADS(MAF)基因以及H3K27三甲基化是必不可少的。这表明其他蛋白质能够抑制FLC,但不能抑制MAF基因的表达。

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