Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0540, USA.
Nat Cell Biol. 2010 Jan;12(1):94-9; sup pp 1-6. doi: 10.1038/ncb2010. Epub 2009 Dec 13.
The 16 kilobase (kb) heterochromatin domain between the chicken beta-globin locus and the folate receptor gene is used here to study the roles of RNA-dependent mechanisms and histone modifications in the maintenance of a constitutive heterochromatic structure. Inhibition of histone deacetylase (HDAC) activity is shown to both increase intergenic transcription and render the heterochromatin more accessible to MspI digestion. We show that short interfering RNA (siRNA)-mediated downregulation of the enzyme Dicer has similar effects: histone acetylation is increased, transcript levels rise and the compact chromatin structure becomes more accessible to restriction endonucleases. We also show that the chicken Argonaute 2 homologue binds the 16 kb region in a Dicer-dependent manner and is necessary for a condensed chromatin structure. Heterochromatic domains of this kind, which are widely distributed in vertebrate genomes, thus seem to be maintained in their condensed form by highly conserved mechanisms.
这里使用鸡β-球蛋白基因座和叶酸受体基因之间的 16 千碱基(kb)异染色质结构域来研究 RNA 依赖性机制和组蛋白修饰在维持组成型异染色质结构中的作用。抑制组蛋白去乙酰化酶(HDAC)的活性不仅增加基因间转录,而且使异染色质更容易被 MspI 消化。我们表明,短干扰 RNA(siRNA)介导的酶 Dicer 的下调具有类似的效果:组蛋白乙酰化增加,转录水平上升,致密染色质结构更容易被限制内切酶消化。我们还表明,鸡 Argonaute 2 同源物以 Dicer 依赖性的方式结合 16 kb 区域,并且对于凝聚的染色质结构是必需的。这种广泛分布在脊椎动物基因组中的异染色质结构域似乎通过高度保守的机制维持其凝聚形式。