Catchpole I, Dyke K G
Department of Biochemistry, University of Oxford, UK.
Mol Microbiol. 1991 Apr;5(4):959-68. doi: 10.1111/j.1365-2958.1991.tb00771.x.
Copy-number mutants of Staphylococcus aureus macrolide-lincosamide-streptogramin B (MLS) resistance plasmid pT48 were isolated by their resistance to the non-inducing macrolide, tylosin. One mutant plasmid, pcopD3, showed a three- to five-fold cis-dominant increase in copy number, and nucleotide sequence analysis revealed that the mutant had a single base change within the replication region. All other pT48 mutants examined had the unusual phenotype of increased plasmid multimerization and elevated copy number. These mutants were effective in trans and DNA sequencing showed that plasmids with this phenotype were deleted in one of two ways. The deletions caused similar alterations to the C-terminus of the wild-type pT48 Rep protein. The two types of mutant Rep proteins terminate with the same pentapeptide sequence: Ala-Asn-Glu-Ile-Asp. The multimerization phenotype of these mutants can be explained by defective termination of rolling-circle type replication.
通过对非诱导性大环内酯类药物泰乐菌素的抗性,分离出了金黄色葡萄球菌大环内酯-林可酰胺-链阳菌素B(MLS)抗性质粒pT48的拷贝数突变体。一个突变体质粒pcopD3的拷贝数呈现出三到五倍的顺式显性增加,核苷酸序列分析表明该突变体在复制区域内有一个单碱基变化。所有检测的其他pT48突变体都具有质粒多聚化增加和拷贝数升高的异常表型。这些突变体在反式作用中有效,DNA测序表明具有这种表型的质粒以两种方式之一发生了缺失。这些缺失对野生型pT48 Rep蛋白的C末端造成了类似的改变。两种类型的突变Rep蛋白都以相同的五肽序列终止:丙氨酸-天冬酰胺-谷氨酸-异亮氨酸-天冬氨酸。这些突变体的多聚化表型可以通过滚环型复制的终止缺陷来解释。