Schermer Ulrike J, Korber Philipp, Hörz Wolfram
Adolf-Butenandt-Institut, Universität München, Germany.
Mol Cell. 2005 Jul 22;19(2):279-85. doi: 10.1016/j.molcel.2005.05.028.
In yeast, remodeling of PHO5 promoter chromatin upon activation is accompanied by transient hyperacetylation and subsequent eviction of histones from the promoter in trans. In the course of rerepression, nucleosomes have to be reassembled on the promoter. We have analyzed where the histones for reassembly of the inactive promoter chromatin come from. The use of a strain with two differently tagged and differently regulated versions of histone H3 allowed us to discriminate between histones originating from the chromatin fraction and histones arising from the soluble histone pool. In this way, we show that the incorporated histones originate from a source in trans. Promoter closure occurs very rapidly, and the histone chaperones Asf1 and Hir1 as well as the SWI/SNF nucleosome remodeling complex appear to be important for rapid reassembly of nucleosomes at the PHO5 promoter.
在酵母中,PHO5启动子染色质在激活时的重塑伴随着短暂的超乙酰化以及随后组蛋白从启动子的反式逐出。在重新抑制过程中,核小体必须在启动子上重新组装。我们分析了用于重新组装无活性启动子染色质的组蛋白的来源。使用具有两个不同标记和不同调控版本的组蛋白H3的菌株,使我们能够区分源自染色质部分的组蛋白和源自可溶性组蛋白池的组蛋白。通过这种方式,我们表明掺入的组蛋白源自反式来源。启动子关闭非常迅速,组蛋白伴侣Asf1和Hir1以及SWI/SNF核小体重塑复合体似乎对PHO5启动子处核小体的快速重新组装很重要。