Morillon Antonin, Karabetsou Nickoletta, Nair Anitha, Mellor Jane
Department of Biochemistry, Division of Molecular Genetics, Oxford, United Kingdom.
Mol Cell. 2005 Jun 10;18(6):723-34. doi: 10.1016/j.molcel.2005.05.009.
Covalent modifications to histones are key epigenetic marks that control gene transcription. Multiple lysine residues on histone H3 are methylated (me), but their functions are unclear. Here, we demonstrate two phases of combinatorial and dynamic H3 methylation during induction of transcription at MET16 in yeast. K4me3 with K36me2/3 define a postinitiation regulatory phase and precede the appearance of K4me2 with K79me2 at the onset of transcript elongation. The Isw1 ATPase delays the release of initiated RNA polymerase II (RNAPII) into elongation to facilitate chromatin modifications. The Spp1 subunit of complex associated with Set1 (COMPASS) and Set2, determining K4me3 and K36me2/3, respectively, are required for transient NuA4-dependent H4K8ac. This releases RNAPII from Isw1 control and promotes controlled transcription elongation and termination. We propose that newly initiated RNAPII is under epigenetic control.
组蛋白的共价修饰是控制基因转录的关键表观遗传标记。组蛋白H3上的多个赖氨酸残基会发生甲基化(me),但其功能尚不清楚。在此,我们展示了酵母中MET16转录诱导过程中组合性和动态性H3甲基化的两个阶段。K4me3与K36me2/3定义了起始后调控阶段,并在转录延伸开始时先于K4me2与K79me2出现。Isw1 ATP酶会延迟起始的RNA聚合酶II(RNAPII)进入延伸阶段,以促进染色质修饰。与Set1(COMPASS)和Set2相关的复合物的Spp1亚基分别决定K4me3和K36me2/3,是短暂的NuA4依赖性H4K8ac所必需的。这将RNAPII从Isw1的控制中释放出来,并促进受控的转录延伸和终止。我们提出新起始的RNAPII处于表观遗传控制之下。