Fonstein M, Haselkorn R
Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637.
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2522-6. doi: 10.1073/pnas.90.6.2522.
A combination of cosmid genome walking and pulsed-field gel electrophoresis was used to construct a high-resolution physical and genetic map of the 3.8-megabase (Mb) genome of Rhodobacter capsulatus SB1003. The mapping was done by hybridization of pulsed-field gel blots and by grouping and further mapping of the cosmids and bacteriophages from genomic libraries. Cosmid clones formed two uninterrupted and ordered groups, one corresponding to the chromosome of R. capsulatus, the other to its 134-kb plasmid. Cos site end-labeling and partial EcoRV digestion of cosmids were used to construct a high-resolution EcoRV map of the genome. Overlapping of the cosmids was confirmed by the resemblance of the cosmid restriction maps and by direct end-to-end hybridization with SP6- and T7-specific transcripts. Twenty-three previously cloned genes and eight groups of repeated sequences, revealed in this work, were located in the ordered gene library and mapped with an accuracy of 1-10 kb. Blots of a minimal set of 192 cosmids, covering the chromosome and the plasmid with the known map position of each cosmid, give to R. capsulatus the same advantages that the Kohara phage panel gives to E. coli.
采用黏粒基因组步移和脉冲场凝胶电泳相结合的方法,构建了荚膜红细菌SB1003 3.8兆碱基(Mb)基因组的高分辨率物理图谱和遗传图谱。通过脉冲场凝胶印迹杂交以及对基因组文库中的黏粒和噬菌体进行分组及进一步定位来完成图谱构建。黏粒克隆形成了两个连续且有序的组,一组对应于荚膜红细菌的染色体,另一组对应于其134 kb的质粒。使用黏粒的Cos位点末端标记和部分EcoRV酶切来构建基因组的高分辨率EcoRV图谱。通过黏粒限制酶图谱的相似性以及与SP6和T7特异性转录本的直接端对端杂交,证实了黏粒的重叠。在这项研究中发现的23个先前克隆的基因和8组重复序列,被定位在有序基因文库中,定位精度为1 - 10 kb。一组最少192个黏粒的印迹,覆盖了染色体和质粒,且每个黏粒都有已知的图谱位置,这赋予了荚膜红细菌与Kohara噬菌体文库赋予大肠杆菌相同的优势。