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小麦胚RNA聚合酶II与克隆的花椰菜花叶病毒DNA结合位点的电子显微镜定位

Electron microscopic mapping of wheat germ RNA polymerase II binding sites on cloned CaMV DNA.

作者信息

Grellet F, Cooke R, Teissere M, Delseny M, Xech J, Penon P

出版信息

Nucleic Acids Res. 1981 Aug 25;9(16):3927-39. doi: 10.1093/nar/9.16.3927.

Abstract

The binding sites of wheat germ RNA polymerase II were mapped on the cloned CaMV genome by observation of enzyme-linear DNA complexes by electron microscopy. Twelve sites are observed. Three of them are relatively stable in the presence of heparin and are found at positions 8-9, 21-23, and 41-44 map units on the physical map of the genome. These positions correspond to AT-rich regions of the viral genome which contain potential promoter sites. These results are discussed with reference to current information on the structure and expression of the CaMV genome.

摘要

通过电子显微镜观察酶与线性DNA复合物,绘制了小麦胚RNA聚合酶II在克隆的花椰菜花叶病毒(CaMV)基因组上的结合位点。观察到12个位点。其中三个在肝素存在下相对稳定,位于基因组物理图谱上8 - 9、21 - 23和41 - 44图谱单位处。这些位置对应于病毒基因组中富含AT的区域,其中包含潜在的启动子位点。结合当前关于CaMV基因组结构和表达的信息对这些结果进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca5b/327406/b439fb33b843/nar00409-0051-a.jpg

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