Yu Kefei, Roy Deepankar, Huang Feng-Ting, Lieber Michael R
Department of Pathology, Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, USA.
Methods Enzymol. 2006;409:316-29. doi: 10.1016/S0076-6879(05)09018-X.
R-loops are structures where an RNA strand is base paired with one DNA strand of a DNA duplex, leaving the displaced DNA strand single-stranded. Stable R-loops exist in vivo at prokaryotic origins of replication, the mitochondrial origin of replication, and mammalian immunoglobulin (Ig) class switch regions in activated B lymphocytes. All of these R-loops arise upon generation of a G-rich RNA strand by an RNA polymerase upon transcription of a C-rich DNA template strand. These R-loops are of significant length. For example, the R-loop at the col E1 origin of replication appears to be about 140 bp. Our own lab has focused on class switch regions, where the R-loops can extend well over a kilobase in length. Here, methods are described for detection and analysis of R-loops in vitro and in vivo.
R环是一种结构,其中一条RNA链与DNA双链体中的一条DNA链碱基配对,使被置换的DNA链保持单链状态。稳定的R环在体内存在于原核生物复制起点、线粒体复制起点以及活化B淋巴细胞中的哺乳动物免疫球蛋白(Ig)类别转换区域。所有这些R环都是在RNA聚合酶转录富含C的DNA模板链时产生富含G的RNA链后形成的。这些R环长度可观。例如,大肠杆菌复制起点处的R环似乎约为140个碱基对。我们自己的实验室专注于类别转换区域,那里的R环长度可以延伸超过一千个碱基。本文介绍了在体外和体内检测与分析R环的方法。