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Novel DNA Sequences from Natural Strains of the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti

机译:固氮共生细菌Sinorhizobium meliloti天然菌株的新型DNA序列。

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摘要

Variation in genome size and content is common among bacterial strains. Identifying these naturally occurring differences can accelerate our understanding of bacterial attributes, such as ecological specialization and genome evolution. In this study, we used representational difference analysis to identify potentially novel sequences not present in the sequenced laboratory strain Rm1021 of the nitrogen-fixing bacterium Sinorhizobium meliloti. Using strain Rm1021 as the driver and the type strain of S. meliloti ATCC 9930, which has a genome size ∼370 kilobases bigger than that of strain Rm1021, as the tester, we identified several groups of sequences in the ATCC 9930 genome not present in strain Rm1021. Among the 85 novel DNA fragments examined, 55 showed no obvious homologs anywhere in the public databases. Of the remaining 30 sequences, 24 contained homologs to the Rm1021 genome as well as unique segments not found in Rm1021, 3 contained sequences homologous to those published for another S. meliloti strain but absent in Rm1021, 2 contained sequences homologous to other symbiotic nitrogen-fixing bacteria (Rhizobium etli and Bradyrhizobium japonicum), and 1 contained a sequence homologous to a gene in a non-nitrogen-fixing species, Pseudomonas sp. NK87. Using PCR, we assayed the distribution of 12 of the above 85 novel sequences in a collection of 59 natural S. meliloti strains. The distribution varied widely among the 12 novel DNA fragments, from 1.7% to 72.9%. No apparent correlation was found between the distribution of these novel DNA sequences and their genotypes obtained using multilocus enzyme electrophoresis. Our results suggest potentially high rates of gene gain and loss in S. meliloti genomes.
机译:基因组大小和含量的变化在细菌菌株中很常见。识别这些自然存在的差异可以加快我们对细菌属性的理解,例如生态专业化和基因组进化。在这项研究中,我们使用代表性差异分析法来鉴定固氮细菌苜蓿中华根瘤菌(Sinorhizobium meliloti)测序实验室菌株Rm1021中不存在的潜在新序列。使用基因组大小比菌株Rm1021大约370千碱基的苜蓿链球菌ATCC 9930型菌株作为驱动子,我们鉴定了ATCC 9930基因组中不存在的几组序列菌株Rm1021在检查的85个新的DNA片段中,有55个在公共数据库中的任何地方都没有显示出明显的同源物。在其余30个序列中,有24个包含与Rm1021基因组同源的序列以及在Rm1021中未发现的独特片段,其中3个包含与另一株苜蓿链球菌菌株公开但在Rm1021中不存在的序列同源,其中2个包含与其他共生氮同源的序列。固定细菌(Rhizobium etli和Bradyrhizobium japonicum),其中1个含有与非固定氮菌Pseudomonas sp。中的基因同源的序列。 NK87。使用PCR,我们测定了上述85种新序列中的12种在59种天然苜蓿链球菌菌株中的分布。在12个新的DNA片段之间的分布差异很大,从1.7%到72.9%。这些新的DNA序列的分布与使用多基因座酶电泳获得的基因型之间没有明显的相关性。我们的结果表明,苜蓿链球菌基因组中潜在的基因获得和丢失率很高。

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