Fajkus J, Nicklas J A, Hancock R
Centre de Recherche en Cancérologie de l'Université Laval Hôtel-Dieu, Québec, Canada.
Mol Gen Genet. 1998 Dec;260(5):410-6. doi: 10.1007/s004380050911.
We have mapped the positions in a approximately 1.4-Mb region of genomic DNA around the human hprt gene which are accessible in vivo to cleavage by topoisomerase II associated with the nuclear matrix. These positions, which are interpreted as the boundaries of DNA loop domains, were mapped in K562 cells by examining the truncation of rare-cutter restriction fragments separated by pulsed field gel electrophoresis after topoisomerase II-mediated cleavage, using seven linked markers mapped in this region as probes for indirect end-labeling. Eleven cleavage positions were detected and were interpreted as defining ten loop domains of lengths between 70 and 210 kb (average approximately 135 kb); the hprt gene resides in a 150-kb loop domain. Loop domain boundaries coincided with three of the fifteen deletion breakpoints mapped in a 600-kb sector of this region in human lymphocytes, within the limits of resolution of pulsed field gel electrophoresis; this correlation was not statistically significant.
我们已经绘制出人类次黄嘌呤磷酸核糖转移酶(hprt)基因周围约1.4兆碱基(Mb)基因组DNA区域内,在体内可被与核基质相关的拓扑异构酶II切割的位置。这些位置被解释为DNA环结构域的边界,通过在拓扑异构酶II介导的切割后,检测脉冲场凝胶电泳分离的稀有切割限制片段的截短情况,在K562细胞中进行定位,使用该区域内定位的七个连锁标记作为间接末端标记的探针。检测到11个切割位置,并将其解释为定义了长度在70至210千碱基(kb)之间(平均约135 kb)的10个环结构域;hprt基因位于一个150 kb的环结构域中。在脉冲场凝胶电泳分辨率范围内,环结构域边界与在人类淋巴细胞该区域600 kb区段中定位的15个缺失断点中的3个重合;这种相关性无统计学意义。