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拟南芥GCN5、HD1和TAF1/HAF2相互作用,以调节光响应基因表达所需的组蛋白乙酰化。

Arabidopsis GCN5, HD1, and TAF1/HAF2 interact to regulate histone acetylation required for light-responsive gene expression.

作者信息

Benhamed Moussa, Bertrand Claire, Servet Caroline, Zhou Dao-Xiu

机构信息

Institut de Biotechnologie des Plantes, Unité Mixte de Recherche 8618, Centre National de la Recherche Scientifique, Université Paris Sud XI, 91405 Orsay, France.

出版信息

Plant Cell. 2006 Nov;18(11):2893-903. doi: 10.1105/tpc.106.043489. Epub 2006 Nov 3.

Abstract

We previously showed that Arabidopsis thaliana histone acetyltransferase TAF1/HAF2 is required for the light regulation of growth and gene expression, and we show here that histone acetyltransferase GCN5 and histone deacetylase HD1/HDA19 are also involved in such regulation. Mutation of GCN5 resulted in a long-hypocotyl phenotype and reduced light-inducible gene expression, whereas mutation of HD1 induced opposite effects. The double mutant gcn5 hd1 restored a normal photomorphogenic phenotype. By contrast, the double mutant gcn5 taf1 resulted in further loss of light-regulated gene expression. gcn5 reduced acetylation of histones H3 and H4, mostly on the core promoter regions, whereas hd1 increased acetylation on both core and more upstream promoter regions. GCN5 and TAF1 were both required for H3K9, H3K27, and H4K12 acetylation on the target promoters, but H3K14 acetylation was dependent only on GCN5. Interestingly, gcn5 taf1 had a cumulative effect mainly on H3K9 acetylation. On the other hand, hd1 induced increased acetylation on H3K9, H3K27, H4K5, and H4K8. GCN5 was also shown to be directly associated with the light-responsive promoters. These results suggest that acetylation of specific histone Lys residues, regulated by GCN5, TAF1, and HD1, is required for light-regulated gene expression.

摘要

我们之前表明,拟南芥组蛋白乙酰转移酶TAF1/HAF2是生长和基因表达的光调节所必需的,并且我们在此表明组蛋白乙酰转移酶GCN5和组蛋白去乙酰化酶HD1/HDA19也参与这种调节。GCN5的突变导致下胚轴伸长的表型以及光诱导基因表达降低,而HD1的突变则产生相反的效果。双突变体gcn5 hd1恢复了正常的光形态建成表型。相比之下,双突变体gcn5 taf1导致光调节基因表达进一步丧失。gcn5降低了组蛋白H3和H4的乙酰化,主要是在核心启动子区域,而hd1增加了核心和更多上游启动子区域的乙酰化。GCN5和TAF1对于靶启动子上的H3K9、H3K27和H4K12乙酰化都是必需的,但H3K14乙酰化仅依赖于GCN5。有趣的是,gcn5 taf1主要对H3K9乙酰化有累积效应。另一方面,hd1诱导H3K9、H3K27、H4K5和H4K8的乙酰化增加。GCN5也被证明与光响应启动子直接相关。这些结果表明,由GCN5、TAF1和HD1调节的特定组蛋白赖氨酸残基的乙酰化是光调节基因表达所必需的。

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