Rivolta C, Pagni M
Institut de Génétique et de Biologie Microbiennes, Université de Lausanne, CH-1005 Lausanne, Switzerland.
Genetics. 1999 Apr;151(4):1239-44. doi: 10.1093/genetics/151.4.1239.
Sequencing of the complete Bacillus subtilis chromosome revealed the presence of approximately 4100 genes, 1000 of which were previously identified and mapped by classical genetic crosses. Comparison of these experimentally determined positions to those derived from the nucleotide sequence showed discrepancies reaching up to 24 degrees (approximately 280 kb). The size of these discrepancies as a function of their position along the chromosome is not random but, apparently, reveals some periodicity. Our analyses demonstrate that the discrepancies can be accounted for by inaccurate positioning of the early reference markers with respect to which all subsequently identified loci were mapped by transduction and transformation. We conclude (i) that specific DNA sequences, such as recombination hotspots or presence of heterologous DNA, had no detectable effect on the results obtained by classical mapping, and (ii) that PBS1 transduction appears to be an accurate and unbiased mapping method in B. subtilis.
枯草芽孢杆菌完整染色体的测序显示存在约4100个基因,其中1000个基因先前已通过经典遗传杂交鉴定并定位。将这些通过实验确定的位置与从核苷酸序列推导的位置进行比较,发现差异高达24度(约280 kb)。这些差异的大小作为其沿染色体位置的函数并非随机,而是显然显示出某种周期性。我们的分析表明,差异可归因于早期参考标记定位不准确,所有后续鉴定的基因座都是相对于这些参考标记通过转导和转化进行定位的。我们得出结论:(i)特定的DNA序列,如重组热点或异源DNA的存在,对经典定位获得的结果没有可检测到的影响;(ii)PBS1转导似乎是枯草芽孢杆菌中一种准确且无偏差的定位方法。