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Alignment of a 1.2-Mb chromosomal region from three strains of Rhodobacter capsulatus reveals a significantly mosaic structure.

机译:来自三种荚膜红细菌菌株的1.2-Mb染色体区域的比对揭示了明显的镶嵌结构。

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摘要

High-resolution physical maps of the genomes of three Rhodobacter capsulatus strains, derived from ordered cosmid libraries, were aligned. The 1.2-Mb segment of the SB1003 genome studied here is adjacent to a 1-Mb region analyzed previously [Fonstein, M., Nikolskaya, T. & Haselkorn, H. (1995) J. Bacteriol. 177, 2368-2372]. Probes derived from the ordered cosmid set of R. capsulatus SB1003 were used to link cosmids from the St. Louis and 2.3.1 strain libraries. Cosmids selected this way did not merge into a single contig but formed several unlinked groups. EcoRV restriction maps of the ordered cosmids were then constructed using lambda terminase and fused to derive fragments of the chromosomal map. In order to link these fragments, their ends were transcribed to produce secondary probes for hybridization to gridded cosmid libraries of the same strains. This linking reduced the number of subcontigs to three for the St. Louis strain and one for the 2.3.1 strain. Hybridization of the same probes back to the ordered cosmid set of SB1003 positioned the subcontigs on the high-resolution physical map of SB1003. The final alignment of the restriction maps shows numerous large and small translocations in this 1.2-Mb chromosomal region of the three Rhodobacter strains. In addition, the chromosomes of the three strains, whose fine-structure maps can now be compared over 2.2 Mb, are seen to contain regions of 15-80 kb in which restriction sites are highly polymorphic, interspersed among regions in which the positions of restriction sites are highly conserved.
机译:对齐从有序的粘粒文库中的三种荚膜红细菌菌株的基因组的高分辨率物理图谱。此处研究的SB1003基因组的1.2 Mb片段与先前分析过的1 Mb区域相邻[Fonstein,M.,Nikolskaya,T.&Haselkorn,H.(1995)J. Bacteriol。 177,2368-2372]。来源于有荚膜的拟南芥SB1003粘粒组的探针用于连接来自圣路易斯和2.3.1菌株库的粘粒。用这种方法选择的粘粒没有合并成一个重叠群,而是形成了几个不相关的基团。然后,使用λ末端酶构建有序粘粒的EcoRV限制性酶切图,并融合以得到染色体图的片段。为了连接这些片段,转录它们的末端以产生用于与相同菌株的网格化粘粒文库杂交的二级探针。这种联系将亚重叠群的数量减少了,圣路易斯菌株为3个,而2.3.1菌株为1个。将相同的探针杂交回SB1003的有序粘粒组,将亚重叠群定位在SB1003的高分辨率物理图上。限制性酶切图谱的最终比对显示了在三种红细菌菌株的这个1.2-Mb染色体区域中的许多大和小的易位。此外,这三个菌株的染色体的精细结构图现在可以比较到2.2 Mb以上,它们的染色体包含15-80 kb的区域,其中限制位点高度多态,散布在限制位置之间网站是高度保守的。

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