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酿酒酵母染色体DNA质粒TRP1 RI环(YARp1)染色质组织的替代模型。

Alternative model for chromatin organization of the Saccharomyces cerevisiae chromosomal DNA plasmid TRP1 RI circle (YARp1).

作者信息

Long C M, Brajkovich C M, Scott J F

出版信息

Mol Cell Biol. 1985 Nov;5(11):3124-30. doi: 10.1128/mcb.5.11.3124-3130.1985.

Abstract

TRP1 RI circle (now designated YARp1, yeast acentric ring plasmid 1) is a 1,453-base-pair artificial plasmid composed exclusively of Saccharomyces cerevisiae chromosomal DNA. It contains both the TRP1 gene and ARS1 (a DNA sequence that permits extrachromosomal maintenance of recombinant plasmids). This high-copy-number, relatively stable plasmid was shown to be organized into nucleosomes comparable to typical yeast chromatin, containing a possible maximum of nine nucleosomes per circle. Therefore, YARp1 can be used to examine the structure of chromatin of both a chromosomally derived replicator and a functional gene. By mapping regions of micrococcal nuclease cleavage in chromatin versus purified DNA, we located the positions of protected regions on the circle with reference to six unique restriction sites. Measurements made on patterns of early digestion products indicated that a region of approximately 300 base pairs in the vicinity of ARS1 was strongly resistant to micrococcal nuclease. The remainder of the plasmid appeared to be associated with five positioned nucleosomes and two nonnucleosomal, partially protected regions on the bulk of the molecules. After similar extents of digestion, naked DNA did not exhibit an equivalent pattern, although some hypersensitive cleavage sites matched sites found in the chromatin. These results are consistent with the interpretation that the protected domains are aligned with respect to a specific site or sites on the small circular chromatin.

摘要

TRP1 RI环(现命名为YARp1,酵母无着丝粒环质粒1)是一种由1453个碱基对组成的人工质粒,完全由酿酒酵母染色体DNA构成。它包含TRP1基因和ARS1(一种能使重组质粒在染色体外维持的DNA序列)。这种高拷贝数、相对稳定的质粒被证明可组装成与典型酵母染色质类似的核小体,每个环最多可能含有9个核小体。因此,YARp1可用于研究染色体衍生复制子和功能基因的染色质结构。通过绘制染色质与纯化DNA中微球菌核酸酶切割区域的图谱,我们参照六个独特的限制性酶切位点确定了环上受保护区域的位置。对早期消化产物模式的测量表明,ARS1附近约300个碱基对的区域对微球菌核酸酶具有很强的抗性。质粒的其余部分似乎与大部分分子上的五个定位核小体以及两个非核小体、部分受保护区域相关。消化程度相似后,裸露DNA并未呈现出等效模式,尽管一些超敏切割位点与染色质中发现的位点相匹配。这些结果与以下解释一致,即受保护结构域相对于小环状染色质上的一个或多个特定位点排列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3739/369127/480d544aa6c0/molcellb00141-0258-a.jpg

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