Asakura Y, Kikuchi Y, Yanagida M
J Biochem. 1985 Jul;98(1):41-7. doi: 10.1093/oxfordjournals.jbchem.a135270.
An S1-hypersensitive site was found at the 60 bp direct repeats of the cis-acting, stability and/or copy number control region of the yeast 2 micron DNA in the supercoiled hybrid plasmid pDB248'. It was retained in a different plasmid, pYK2121, consisting of pBR322 and the 300 bp long repeated DNA. Analyses of 5'-end-labeled fragments and nucleotide sequence determination showed that the S1-cleavage site was at the central part of an AT-rich 19 bp palindrome present in the repeats. Two other homologous palindromes (21 and 15 bp) containing the 12 bp consensus sequences were not cleaved. The nucleotide sequences at the base of the stem and/or loop may determine the efficiency of the cruciform extrusion.
在超螺旋杂交质粒pDB248'中,于酵母2μm DNA顺式作用、稳定性和/或拷贝数控制区的60bp直接重复序列处发现了一个S1超敏位点。它保留在另一个由pBR322和300bp长的重复DNA组成的质粒pYK2121中。对5'端标记片段的分析和核苷酸序列测定表明,S1切割位点位于重复序列中一个富含AT的19bp回文序列的中央部分。另外两个含有12bp共有序列的同源回文序列(21bp和15bp)未被切割。茎和/或环底部的核苷酸序列可能决定十字形挤出的效率。