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通过电子显微镜测定BAL 31 RNA聚合酶与PM2 DNA的结合以及对限制性内切核酸酶切割的保护作用。

Binding of BAL 31 RNA polymerase to PM2 DNA as determined by electron microscopy and protection against restriction endonuclease cleavage.

作者信息

Bull P, Susaeta M, González B, Yudelevich A

机构信息

Laboratorio de Bioquímica, Pontificia Universidad Católica de Chile, Santiago.

出版信息

J Virol. 1988 Oct;62(10):3911-3. doi: 10.1128/JVI.62.10.3911-3913.1988.

Abstract

Specific binding sites of BAL 31 RNA polymerase on PM2 DNA have been mapped by protection against HincII and HindIII cleavage and by observation of enzyme-DNA complexes by electron microscopy. Nine specific binding sites were observed at map units 0.19, 0.20, 0.28, 0.54, 0.63, 0.65, 0.71, 0.72, and 0.75 by the first method. All these sites were confirmed by electron microscopy which, in addition, revealed another site at 0.05 map unit. Published nucleotide sequences of the region surrounding sites at 0.71 and 0.75 map units show the presence of consensus sequences for procaryotic promoters.

摘要

通过防止HincII和HindIII切割以及通过电子显微镜观察酶 - DNA复合物,已绘制出BAL 31 RNA聚合酶在PM2 DNA上的特异性结合位点。通过第一种方法,在图谱单位0.19、0.20、0.28、0.54、0.63、0.65、0.71、0.72和0.75处观察到9个特异性结合位点。所有这些位点均通过电子显微镜得到证实,此外,电子显微镜还揭示了在图谱单位0.05处的另一个位点。已发表的在图谱单位0.71和0.75处位点周围区域的核苷酸序列显示存在原核启动子的共有序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0946/253545/6a9492cf60e9/jvirol00089-0380-a.jpg

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