Fonstein M, Koshy E G, Nikolskaya T, Mourachov P, Haselkorn R
Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637, USA.
EMBO J. 1995 Apr 18;14(8):1827-41. doi: 10.1002/j.1460-2075.1995.tb07171.x.
Cosmids from a library containing Rhodobacter capsulatus DNA fragments were previously ordered in two contigs: one corresponding to the chromosome and one to a 134 kb plasmid. This map contained 40 regions connected only by colony hybridization. To confirm the linkage and correct the map, the actual sizes of the overlaps were determined by blot-hybridization with Rhodobacter chromosomal DNA and by mapping of additional cosmids. Several revisions of the earlier map include single cosmid shifts and inversions. One additional gap in a cosmid contig was also found, raising the possibility that the chromosome is not a contiguous circle. About 2500 additional EcoRI,BamHI and HindIII restriction sites were added to the 560 EcoRV sites previously mapped onto the Rhodobacter chromosome, increasing the resolution of the physical map to the size of individual genes. Twenty-five new markers were located on the genetic map. The 48 markers now mapped represent nearly 300 genes and ORFs cloned from different species of Rhodobacter. The orientation of transcription of the four rrn operons was established using 16S rRNA- and 23S rRNA-specific probes and digestion with the rare-cutting enzyme, CeuI. Gel blots of 192 cosmids of the miniset of R.capsulatus digested with EcoRV were prepared. Such a hybridization template represents the whole genome cut into 560 DNA fragments varying in size from 0.4 to 25 kb. This template was used for high-resolution mapping of single genes, analysis of total genomic DNAs from related Rhodobacter strains and differentially expressed RNAs.
来自一个包含荚膜红细菌DNA片段文库的黏粒先前被排列成两个重叠群:一个对应于染色体,另一个对应于一个134 kb的质粒。该图谱包含仅通过菌落杂交连接的40个区域。为了确认连锁关系并校正图谱,通过与荚膜红细菌染色体DNA进行印迹杂交以及对额外黏粒进行定位来确定重叠部分的实际大小。对早期图谱的几次修订包括单个黏粒的移位和倒位。在一个黏粒重叠群中还发现了另外一个缺口,这增加了染色体不是连续环状的可能性。在先前绘制到荚膜红细菌染色体上的560个EcoRV位点的基础上,又增加了约2500个额外的EcoRI、BamHI和HindIII限制性酶切位点,将物理图谱的分辨率提高到单个基因的大小。在遗传图谱上定位了25个新标记。现在绘制的48个标记代表了从不同荚膜红细菌物种克隆的近300个基因和开放阅读框。使用16S rRNA和23S rRNA特异性探针以及用稀有切割酶CeuI消化,确定了四个rrn操纵子的转录方向。制备了用EcoRV消化的荚膜红细菌小型文库中192个黏粒的凝胶印迹。这样的杂交模板代表了被切割成大小从0.4到25 kb不等的560个DNA片段的整个基因组。该模板用于单个基因的高分辨率定位、相关荚膜红细菌菌株的总基因组DNA分析以及差异表达RNA的分析。