Wang X M, Chang C H, Waddell J, Wu M
Nucleic Acids Res. 1984 May 11;12(9):3857-72. doi: 10.1093/nar/12.9.3857.
The EcoR1 restriction fragments containing D-loops which marked the replication origin of chloroplast DNA were identified in two different species of Chlamydomonas. Each fragment was cloned in the E. coli plasmid pBR325. The cloned fragments were compared by restriction endonuclease analyses and by heteroduplex analyses in the electron microscope. The relative position of the D-loop regions and the homologous regions between the 2 fragments was determined. The D-loops were located within one short homologous region of 0. 42kb in length between the 2 cloned restriction fragments. The homologous region was subcloned in pBR322. Closed circular plasmid DNAs containing the short homologous region showed preferred denaturation in the D-loop region under physiological salt concentration which suggested that D-loop region was AT rich. Sequence divergence was detected at both ends of the D-loop region. Southern blot analyses indicated the presence of species-specific repetitive sequences within the divergent regions.
在两种不同的衣藻属物种中鉴定出了含有标记叶绿体DNA复制起点的D环的EcoR1限制性片段。每个片段都克隆到大肠杆菌质粒pBR325中。通过限制性内切酶分析和电子显微镜下的异源双链分析对克隆片段进行比较。确定了D环区域和两个片段之间同源区域的相对位置。D环位于两个克隆的限制性片段之间一个长度为0.42kb的短同源区域内。该同源区域被亚克隆到pBR322中。含有短同源区域的闭环质粒DNA在生理盐浓度下在D环区域表现出优先变性,这表明D环区域富含AT。在D环区域的两端检测到序列差异。Southern印迹分析表明在差异区域内存在物种特异性重复序列。