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CHD3 重塑因子 PICKLE 与富含组蛋白 H3 赖氨酸 27 三甲基化的基因相关。

The CHD3 remodeler PICKLE associates with genes enriched for trimethylation of histone H3 lysine 27.

机构信息

Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

Plant Physiol. 2012 May;159(1):418-32. doi: 10.1104/pp.112.194878. Epub 2012 Mar 27.

Abstract

In Arabidopsis (Arabidopsis thaliana), the ATP-dependent chromatin remodeler PICKLE (PKL) determines expression of genes associated with developmental identity. PKL promotes the epigenetic mark trimethylation of histone H3 lysine 27 (H3K27me3) that facilitates repression of tissue-specific genes in plants. It has previously been proposed that PKL acts indirectly to promote H3K27me3 by promoting expression of the POLYCOMB REPRESSIVE COMPLEX2 complex that generates H3K27me3. We undertook expression and chromatin immunoprecipitation analyses to further characterize the contribution of PKL to gene expression and developmental identity. Our expression data support a critical and specific role for PKL in expression of H3K27me3-enriched loci but do not support a role for PKL in expression of POLYCOMB REPRESSIVE COMPLEX2. Moreover, our chromatin immunoprecipitation data reveal that PKL protein is present at the promoter region of multiple H3K27me3-enriched loci, indicating that PKL directly acts on these loci. In particular, we find that PKL is present at LEAFY COTYLEDON1 and LEAFY COTYLEDON2 during germination, which is when PKL acts to repress these master regulators of embryonic identity. Surprisingly, we also find that PKL is present at the promoters of actively transcribed genes that are ubiquitously expressed such as ACTIN7 and POLYUBIQUITIN10 that do not exhibit PKL-dependent expression. Taken together, our data contravene the previous model of PKL action and instead support a direct role for PKL in determining levels of H3K27me3 at repressed loci. Our data also raise the possibility that PKL facilitates a common chromatin remodeling process that is not restricted to H3K27me3-enriched regions.

摘要

在拟南芥(Arabidopsis thaliana)中,ATP 依赖性染色质重塑酶 PICKLE(PKL)决定与发育身份相关的基因的表达。PKL 促进组蛋白 H3 赖氨酸 27 三甲基化(H3K27me3)的表观遗传标记,促进植物中组织特异性基因的抑制。先前已经提出,PKL 通过促进多梳抑制复合物 2(产生 H3K27me3)复合物的表达来间接促进 H3K27me3 的表达,从而发挥作用。我们进行了表达和染色质免疫沉淀分析,以进一步表征 PKL 对基因表达和发育身份的贡献。我们的表达数据支持 PKL 在富含 H3K27me3 的基因座表达中具有关键和特异性作用,但不支持 PKL 在多梳抑制复合物 2 表达中的作用。此外,我们的染色质免疫沉淀数据显示,PKL 蛋白存在于多个富含 H3K27me3 的基因座的启动子区域,表明 PKL 直接作用于这些基因座。特别是,我们发现 PKL 在萌发期间存在于 LEAFY COTYLEDON1 和 LEAFY COTYLEDON2 的启动子区域,这是 PKL 发挥作用抑制这些胚胎身份的主要调控因子的时候。令人惊讶的是,我们还发现 PKL 存在于 ACTIN7 和 POLYUBIQUITIN10 等广泛表达的活跃转录基因的启动子中,这些基因不表现出依赖 PKL 的表达。总的来说,我们的数据与 PKL 作用的先前模型相矛盾,而是支持 PKL 在决定受抑制基因座的 H3K27me3 水平方面的直接作用。我们的数据还提出了一种可能性,即 PKL 促进了一种常见的染色质重塑过程,而不仅仅局限于富含 H3K27me3 的区域。

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