Lyamichev V I, Panyutin I G, Cherny D I
Nucleic Acids Res. 1983 Apr 11;11(7):2165-76. doi: 10.1093/nar/11.7.2165.
Specific fragmentation of T7 DNA at glyoxal-fixed denatured regions by the S1 endonuclease followed by restriction analysis made it possible to localize four low-melting regions in phage T7 DNA. These regions have the following coordinates:0.5-1.2;14.8+/-0.3;46.3+/-0.5; 98.4+/-0.3 (in T7 DNA length units). The location of the low-melting regions was refined by means of electron-microscopic denaturation mapping and gel electrophoresis of partially denatured DNA. The obtained localization of the low-melting regions is consistent with the available data on the sequence of T7 DNA. The map of low-melting regions was compared with the genetic map of T7 DNA.Images
通过S1核酸内切酶对乙二醛固定的变性区域的T7 DNA进行特异性切割,随后进行限制性分析,使得在噬菌体T7 DNA中定位四个低熔点区域成为可能。这些区域具有以下坐标:0.5 - 1.2;14.8±0.3;46.3±0.5;98.4±0.3(以T7 DNA长度单位计)。通过电子显微镜变性图谱和部分变性DNA的凝胶电泳对低熔点区域的位置进行了细化。所获得的低熔点区域的定位与关于T7 DNA序列的现有数据一致。将低熔点区域的图谱与T7 DNA的遗传图谱进行了比较。图像