Nejedlý K, Kittner R, Kypr J
Institute of Biophysics of the Academy of Sciences of the Czech Republic, Brno.
Arch Biochem Biophys. 2001 Apr 15;388(2):216-24. doi: 10.1006/abbi.2001.2280.
We prepared an extensive set of DNA restriction fragments, irradiated them with UV light, and detected crosslinked complementary strands by electrophoresis in denaturing agarose gels. These experimental data were quantified by densitometry to determine tetranucleotide contributions to crosslinking. The tetranucleotide contributions were used to predict genomic maps of the crosslinking probability that permitted us to identify two strongly crosslinking genomic regions having 295 and 389 base pairs in length. The two sequences shared the (ATTTTATA).(TATAAAAT) octamer, which is a candidate for the hotspot of UV light-induced crosslinking between the complementary strands of DNA.
我们制备了大量的DNA限制性片段,用紫外线照射它们,并通过在变性琼脂糖凝胶中电泳检测交联的互补链。通过光密度测定法对这些实验数据进行定量,以确定四核苷酸对交联的贡献。四核苷酸的贡献用于预测交联概率的基因组图谱,这使我们能够识别出两个长度分别为295和389个碱基对的强烈交联基因组区域。这两个序列共享(ATTTTATA).(TATAAAAT)八聚体,它是DNA互补链之间紫外线诱导交联热点的候选序列。