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Chromatin structures and transcription of rDNA in yeast Saccharomyces cerevisiae

机译:酿酒酵母中的染色质结构和rDNA的转录

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The chromatin structure of yeast ribosomal DNA was analyzed In vivo by crosslinklng Intact cells with psoralen. We found that In exponentially growing cultures the regions coding for the 35S rRNA precursor fall Into two distinct classes. One class was highly accessible to psoralen and associated with nascent RNAs, characteristic for transcriptionally active rRNA genes devoid of nucleosomes, whereas the other class showed a crosslinklng pattern indistinguishable from that of bulk chromatin and was Interpreted to represent the Inactive rRNA gene copies. By crosslinking the same strain growing in complex or minimal medium, we have shown that yeast cells can modulate the proportion of active (non-nucleosomal) and inactive (nucleosomal) rRNA gene copies In response to variations In environmental conditions which suggests that yeast can regulate rRNA synthesis by varying the number of active gene copies, In contrast to the vertebrate cells studied so far. Whereas Intergenic spacers flanking Inactive rRNA gene copies are packaged in a regular nucleosomal array, spacers flanking active genes show an unusual crosslinking pattern suggesting a complex Interaction of regulatory factors and histones with DNA.
机译:通过将完整细胞与补骨脂素交联,在体内分析了酵母核糖体DNA的染色质结构。我们发现在指数增长的文化中,编码35S rRNA前体的区域分为两个不同的类别。一类很容易补骨脂素并与新生RNA相关联,这是不含核小体的转录活性rRNA基因的特征,而另一类则显示出与大量染色质无法区分的交联模式,并被解释为代表非活性rRNA基因拷贝。通过交联在复杂或基本培养基中生长的同一菌株,我们已经表明,酵母细胞可以调节活性(非核小体)和无活性(核小体)rRNA基因拷贝的比例,以响应环境条件下的变化,这表明酵母可以调节与迄今为止研究的脊椎动物细胞相比,通过改变活性基因拷贝数来合成rRNA。侧翼位于非活性rRNA基因拷贝的基因间隔子以规则的核小体阵列包装,而侧翼活性基因的间隔子表现出不寻常的交联模式,表明调节因子和组蛋白与DNA的复杂相互作用。

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