Genome Research Center, NODAI Research Institute, Tokyo University of Agriculture, Tokyo, Japan.
PLoS One. 2011 Jan 28;6(1):e16372. doi: 10.1371/journal.pone.0016372.
In order to elucidate the influence of histone acetylation upon nucleosomal DNA length and nucleosome position, we compared nucleosome maps of the following three yeast strains; strain BY4741 (control), the elp3 (one of histone acetyltransferase genes) deletion mutant, and the hos2 (one of histone deactylase genes) deletion mutant of Saccharomyces cerevisiae. We sequenced mononucleosomal DNA fragments after treatment with micrococcal nuclease. After mapping the DNA fragments to the genome, we identified the nucleosome positions. We showed that the distributions of the nucleosomal DNA lengths of the control and the hos2 disruptant were similar. On the other hand, the distribution of the nucleosomal DNA lengths of the elp3 disruptant shifted toward shorter than that of the control. It strongly suggests that inhibition of Elp3-induced histone acetylation causes the nucleosomal DNA length reduction. Next, we compared the profiles of nucleosome mapping numbers in gene promoter regions between the control and the disruptant. We detected 24 genes with low conservation level of nucleosome positions in promoters between the control and the elp3 disruptant as well as between the control and the hos2 disruptant. It indicates that both Elp3-induced acetylation and Hos2-induced deacetylation influence the nucleosome positions in the promoters of those 24 genes. Interestingly, in 19 of the 24 genes, the profiles of nucleosome mapping numbers were similar between the two disruptants.
为了阐明组蛋白乙酰化对核小体 DNA 长度和核小体位置的影响,我们比较了以下三种酵母菌株的核小体图谱:BY4741 菌株(对照)、elp3(组蛋白乙酰转移酶基因之一)缺失突变体和 hos2(组蛋白去乙酰化酶基因之一)缺失突变体。我们用微球菌核酸酶处理后对单核小体 DNA 片段进行测序。将 DNA 片段映射到基因组后,我们确定了核小体的位置。我们发现对照和 hos2 破坏体的核小体 DNA 长度分布相似。另一方面,elp3 破坏体的核小体 DNA 长度分布向短于对照的方向移动。这强烈表明抑制 Elp3 诱导的组蛋白乙酰化导致核小体 DNA 长度减少。接下来,我们比较了对照和破坏体基因启动子区域核小体作图数量的分布。我们在控制和 elp3 破坏体以及控制和 hos2 破坏体之间的启动子中检测到 24 个基因的核小体位置低保守水平。这表明 Elp3 诱导的乙酰化和 Hos2 诱导的去乙酰化都影响了这 24 个基因启动子中的核小体位置。有趣的是,在 24 个基因中的 19 个中,两个破坏体之间的核小体作图数量的分布相似。