Earley Keith, Lawrence Richard J, Pontes Olga, Reuther Rachel, Enciso Angel J, Silva Manuela, Neves Nuno, Gross Michael, Viegas Wanda, Pikaard Craig S
Biology Department, Washington University, St. Louis, Missouri 63130, USA.
Genes Dev. 2006 May 15;20(10):1283-93. doi: 10.1101/gad.1417706. Epub 2006 Apr 28.
Nucleolar dominance describes the silencing of one parental set of ribosomal RNA (rRNA) genes in a genetic hybrid, an epigenetic phenomenon that occurs on a scale second only to X-chromosome inactivation in mammals. An RNA interference (RNAi) knockdown screen revealed that the predicted Arabidopsis histone deacetylase, HDA6, is required for rRNA gene silencing in nucleolar dominance. In vivo, derepression of silenced rRNA genes upon knockdown of HDA6 is accompanied by nucleolus organizer region (NOR) decondensation, loss of promoter cytosine methylation, and replacement of histone H3 Lys 9 (H3K9) dimethylation with H3K4 trimethylation, H3K9 acetylation, H3K14 acetylation, and histone H4 tetra-acetylation. Consistent with these in vivo results, purified HDA6 deacetylates lysines modified by histone acetyltransferases whose substrates include H3K14, H4K5, and H4K12. HDA6 localizes, in part, to the nucleolus, supporting a model whereby HDA6 erases histone acetylation as a key step in an epigenetic switch mechanism that silences rRNA genes through concerted histone and DNA modifications.
核仁显性描述了遗传杂种中一组亲本核糖体RNA(rRNA)基因的沉默,这是一种表观遗传现象,其发生规模仅次于哺乳动物中的X染色体失活。一项RNA干扰(RNAi)敲低筛选显示,预测的拟南芥组蛋白脱乙酰酶HDA6是核仁显性中rRNA基因沉默所必需的。在体内,HDA6敲低后沉默的rRNA基因去抑制伴随着核仁组织区(NOR)解聚、启动子胞嘧啶甲基化丧失,以及组蛋白H3赖氨酸9(H3K9)二甲基化被H3K4三甲基化、H3K9乙酰化、H3K14乙酰化和组蛋白H4四乙酰化所取代。与这些体内结果一致,纯化的HDA6使由组蛋白乙酰转移酶修饰的赖氨酸脱乙酰化,这些组蛋白乙酰转移酶的底物包括H3K14、H4K5和H4K12。HDA6部分定位于核仁,支持了一个模型,即HDA6消除组蛋白乙酰化是表观遗传开关机制中的关键步骤,该机制通过协调组蛋白和DNA修饰使rRNA基因沉默。