Inouye S
FEBS Lett. 1984 Jul 9;172(2):231-4. doi: 10.1016/0014-5793(84)81131-x.
The breakage of double-strand (ds) DNA by 13-L-hydroperoxy-cis-9,trans-11-octadecadienoic acid (LAHPO) was investigated by agarose gel electrophoresis of supercoiled pBR322 DNA and the site of cleavage on the DNA molecule was determined by the method of DNA sequence analysis using 3'-end and 5'-end-labeled DNA fragments as substrates. LAHPO caused cleavage at the position of guanine nucleotide in dsDNA. LAHPO caused dsDNA breaks at specific sites, but linoleic acid (LA) and 13-L-hydroxy-cis-9,trans-11-octadecadienoic acid (LAHO) have no such effects on dsDNA. The active oxygen atom of the hydroperoxy group of LAHPO was perhaps responsible for the site-specific cleavage of dsDNA.
通过超螺旋pBR322 DNA的琼脂糖凝胶电泳研究了13-L-氢过氧-顺-9,反-11-十八碳二烯酸(LAHPO)对双链(ds)DNA的断裂作用,并以3'-末端和5'-末端标记的DNA片段为底物,采用DNA序列分析方法确定了DNA分子上的切割位点。LAHPO在dsDNA的鸟嘌呤核苷酸位置引起切割。LAHPO在特定位点导致dsDNA断裂,但亚油酸(LA)和13-L-羟基-顺-9,反-11-十八碳二烯酸(LAHO)对dsDNA没有这种作用。LAHPO氢过氧基的活性氧原子可能是dsDNA位点特异性切割的原因。