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Corepressor-Directed Preacetylation of Histone H3 in Promoter Chromatin Primes Rapid Transcriptional Switching of Cell-Type-Specific Genes in Yeast

机译:启动子染色质中组蛋白H3的Corepressor指导的预乙酰化引发酵母中细胞类型特定基因的快速转录转换。

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摘要

Switching between alternate states of gene transcription is fundamental to a multitude of cellular regulatory pathways, including those that govern differentiation. In spite of the progress in our understanding of such transitions in gene activity, a major unanswered question is how cells regulate the timing of these switches. Here, we have examined the kinetics of a transcriptional switch that accompanies the differentiation of yeast cells of one mating type into a distinct new cell type. We found that cell-type-specific genes silenced by the α2 repressor in the starting state are derepressed to establish the new mating-type-specific gene expression program coincident with the loss of α2 from promoters. This rapid derepression does not require the preloading of RNA polymerase II or a preinitiation complex but instead depends upon the Gcn5 histone acetyltransferase. Surprisingly, Gcn5-dependent acetylation of nucleosomes in the promoters of mating-type-specific genes requires the corepressor Ssn6-Tup1 even in the repressed state. Gcn5 partially acetylates the amino-terminal tails of histone H3 in repressed promoters, thereby priming them for rapid derepression upon loss of α2. Thus, Ssn6-Tup1 not only efficiently represses these target promoters but also functions to initiate derepression by creating a chromatin state poised for rapid activation.
机译:基因转录的交替状态之间的切换是众多细胞调控途径(包括控制分化的调控途径)的基础。尽管我们对基因活性的这种转变的理解有所进步,但一个主要的未解决问题是细胞如何调节这些开关的时间。在这里,我们已经研究了一种转录转换的动力学,该动力学伴随着一种交配类型的酵母细胞分化为一种独特的新细胞类型。我们发现在启动状态下被α2阻遏物沉默的细胞类型特异性基因被抑制,以建立与启动子丢失α2相符的新的交配类型特异性基因表达程序。这种快速的抑制作用不需要RNA聚合酶II或预启动复合物的预加载,而是取决于Gcn5组蛋白乙酰转移酶。出人意料的是,交配型特异性基因启动子中核小体的Gcn5依赖性乙酰化即使在受阻状态下也需要共抑制因子Ssn6-Tup1。 Gcn5在阻抑的启动子中部分乙酰化组蛋白H3的氨基末端尾巴,从而引发它们以使其在α2丢失时迅速去抑制。因此,Ssn6-Tup1不仅有效地抑制了这些靶启动子,而且还通过产生准备快速激活的染色质状态来启动去阻遏作用。

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