Goding C R, Russell W C
Nucleic Acids Res. 1983 Jan 11;11(1):21-36. doi: 10.1093/nar/11.1.21.
S1 nuclease has been used as a probe for regions of DNA secondary structure in supercoiled recombinant plasmids containing adenovirus (Ad) DNA sequences. In the sequences examined two S1 sensitive sites were identified in the left-terminal 16.5% of Ad 12 DNA, one of which aligned approximately with an inverted repeat region in the DNA sequence. In addition an S1 sensitive site was dictated by a potential cruciform structure in the region of the Ad 2 major late promoter. In contrast to the expected cleavage site at the loop of the cruciform, cleavage occurred at the base of the stem in the region of the TATA box. All three S1 sensitive sites identified were more sensitive to S1 than the endogenous sites in the parent plasmids.
S1核酸酶已被用作探测含有腺病毒(Ad)DNA序列的超螺旋重组质粒中DNA二级结构区域的探针。在所检测的序列中,在Ad 12 DNA左末端16.5%区域鉴定出两个S1敏感位点,其中一个位点大致与DNA序列中的一个反向重复区域对齐。此外,Ad 2主要晚期启动子区域的一个潜在十字形结构决定了一个S1敏感位点。与十字形环处预期的切割位点相反,切割发生在TATA盒区域茎的基部。所鉴定的所有三个S1敏感位点对S1的敏感性均高于亲本质粒中的内源性位点。