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脱氧核糖核酸酶I、脱氧核糖核酸酶II和葡萄球菌核酸酶在核小体核心中不同但对称分布的位点进行切割。

DNAase I, DNAase II and staphylococcal nuclease cut at different, yet symmetrically located, sites in the nucleosome core.

作者信息

Sollner-Webb B, Melchior W, Felsenfeld G

出版信息

Cell. 1978 Jul;14(3):611-27. doi: 10.1016/0092-8674(78)90246-5.

Abstract

We have determined the relative location of pancreatic DNAase (DNAase I), spleen acid DNAase (DNAase II) and staphylococcal nuclease cleavage sites in the nucleosome core. Each of these three enzymes cleaves the DNA of chromatin at 10.n nucleotide intervals (n integer); this specificity presumably reflects the internal structure of the nucleosome. We have already reported that DNAase I cleaves nucleosomal DNA so that nearest adjacent cuts on opposite strands are staggered by 2 nucleotides, 3' end extending (Sollner-Webb and Felsenfeld, 1977). Here we show that the nearest cuts made by DNAase II in nucleosomal DNA are staggered by 4 nucleotides, 3' end extending, while cuts made by staphylococcal nuclease have a stagger of 2 nucleotides, 5' end extending. The cutting sites of the three enzymes thus do not coincide. Each pair of staggered cuts, however, is symmetrically located about a common axis-that is, the "dyad axes" that bisect nearest pairs of cutting sites coincide for all three enzymes. This result is consistent with the presence of a true dyad axis in the nucleosome core. Our results support the conclusion that a structural feature of the nucleosome, having a 10 nucleotide periodicity, is the common recognition site for all three nucleases. The position of the cut is determined, however, by the individual characteristics of each enzyme. Sites potentially available to nuclease cleavage span a region of 4 nucleotides out of this 10 nucleotide repeat, and a large fraction of these sites are actually cut. Thus much of the nucleosomal DNA must in some sense be accessible to the environment.

摘要

我们已经确定了胰腺DNA酶(DNA酶I)、脾脏酸性DNA酶(DNA酶II)和葡萄球菌核酸酶在核小体核心中的切割位点的相对位置。这三种酶中的每一种都以10n个核苷酸的间隔(n为整数)切割染色质的DNA;这种特异性大概反映了核小体的内部结构。我们已经报道过,DNA酶I切割核小体DNA,使得相对链上最近的相邻切割位点错开2个核苷酸,3'端延伸(索尔纳-韦伯和费尔森菲尔德,1977年)。在这里我们表明,DNA酶II在核小体DNA中产生的最近切割位点错开4个核苷酸,3'端延伸,而葡萄球菌核酸酶产生的切割位点错开2个核苷酸,5'端延伸。因此,这三种酶的切割位点并不重合。然而,每对错开的切割位点围绕一个共同的轴对称定位——也就是说,平分最近切割位点对的“二分轴”对所有三种酶来说是重合的。这一结果与核小体核心中存在真正的二分轴是一致的。我们的结果支持这样的结论,即具有10个核苷酸周期性的核小体结构特征是所有三种核酸酶的共同识别位点。然而,切割的位置是由每种酶的个体特性决定的。核酸酶切割的潜在可用位点跨越这10个核苷酸重复中的4个核苷酸区域,并且这些位点中的很大一部分实际上被切割了。因此,在某种意义上,核小体的许多DNA必须对环境是可及的。

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