Pasero P, Marilley M
Laboratoire de Génétique, URA CNRS 1189, Faculté de Médecine, Marseille, France.
Mol Gen Genet. 1993 Jan;236(2-3):448-52. doi: 10.1007/BF00277147.
The higher-order organization of rRNA genes was investigated in the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe. We used pulsed-field gel electrophoresis (PFGE) in combination with frequent cutter endonucleases having no recognition sites within rDNA repeating units to characterize tandem arrays of ribosomal genes in these two species. Large variations in rDNA cluster length were detected in various S. cerevisiae and S. pombe strains commonly used as PFGE molecular weight markers. This wide range of variability implies that the sizes currently assessed for chromosomes bearing rRNA genes in these organisms are unreliable since they may vary within strains by several hundreds of kilobase pairs, depending on the size of the tandem arrays of rRNA genes. Consequently, there is now a lack of reliable PFGE size standards between 1.6 Mb and 4.5 Mb, even when established yeast strains with calibrated chromosomes are used.
在酿酒酵母和粟酒裂殖酵母中研究了rRNA基因的高级组织。我们使用脉冲场凝胶电泳(PFGE)结合在rDNA重复单元内没有识别位点的频繁切割核酸内切酶,来表征这两个物种中核糖体基因的串联阵列。在常用作PFGE分子量标记的各种酿酒酵母和粟酒裂殖酵母菌株中检测到rDNA簇长度的巨大差异。这种广泛的变异性意味着目前评估的这些生物体中携带rRNA基因的染色体大小是不可靠的,因为它们可能在菌株内相差数百千碱基对,这取决于rRNA基因串联阵列的大小。因此,即使使用具有校准染色体的既定酵母菌株,目前在1.6 Mb至4.5 Mb之间也缺乏可靠的PFGE大小标准。