Shen C K
Nucleic Acids Res. 1983 Nov 25;11(22):7899-910. doi: 10.1093/nar/11.22.7899.
Supercoiled recombinant DNAs containing the human adult alpha-globin gene region have been probed with nuclease S1 in vitro. While agarose gel electrophoresis showed only one predominant, double-stranded cleavage generated by S1 within 6 kb of human DNA and 4 kb of pBR322 sequence, a high resolution gel analysis reveals that the unique S1-hypersensitive locus in the human adult alpha-globin gene region actually contains more than 15 authentic S1 cleavage sites closely spaced together. The mapping approach used here locates the specific S1 cleavage sites on both DNA strands at the nucleotide sequence level. Interestingly, most of these sites are mapped within a 90 bp stretch of GC-rich (66%) polypyrimidine . polypurine DNA that is located 1060 to 1150 bp upstream from alpha 1-globin gene. These results provide the first high resolution map of double-stranded S1-cleavage sites induced within a specific DNA sequence under supercoil strain. The distribution and relative cutting frequencies of these sites mapped are consistent with a slippage mechanism in which the simple repeating sequences are organized into base-mismatched duplex on supercoiled DNA.
已在体外用人核酸酶S1对含有成人人类α-珠蛋白基因区域的超螺旋重组DNA进行了探测。虽然琼脂糖凝胶电泳显示在人类DNA的6 kb和pBR322序列的4 kb范围内,S1仅产生了一个主要的双链切割,但高分辨率凝胶分析表明,成人人类α-珠蛋白基因区域中独特的S1超敏位点实际上包含15个以上紧密排列在一起的真实S1切割位点。这里使用的定位方法在核苷酸序列水平上确定了两条DNA链上的特定S1切割位点。有趣的是,这些位点大多位于富含GC(66%)的多嘧啶-多嘌呤DNA的90 bp片段内,该片段位于α1-珠蛋白基因上游1060至1150 bp处。这些结果提供了超螺旋应变下特定DNA序列内诱导产生的双链S1切割位点的首张高分辨率图谱。所定位的这些位点的分布和相对切割频率与一种滑动机制一致,在该机制中,简单重复序列在超螺旋DNA上被组织成碱基错配的双链体。