Tietze E, Tschäpe H
Bundesgesundheitsamt, Robert-Koch-Institut, Wernigerode, FRG.
J Basic Microbiol. 1994;34(2):105-16. doi: 10.1002/jobm.3620340206.
A 1,3 kb DNA fragment of the IncM plasmid R446, if cloned in a multicopy plasmid, inhibits in trans the expression of conjugation pili by IncM plasmid-harbouring host bacteria as indicated by their insensitivity to the IncM pilus-dependent bacteriophage phi M (Iml, insensitivity to phi M-mediated lysis). Determination of the nucleotide sequence of this DNA fragment, the introduction of deletions an the analysis of transposon insertions reveal two determinants, imlA and imlB, responsible for the Iml phenotype. A stretch of 80 bp of DNA containing imlA and about 450 bp of adjacent DNA comprising imlB, together, bring about inhibition of the typical expression of conjugation pili at 30 degrees C. The introduction of a transposable promoter probe and the construction of respective lacZ fusions indicate transcription of complementary strands in vivo overlapping in the region comprising imlA and imlB. Moreover, the expression of reporter genes discloses temperature-dependent transcription of the imlA-imlB-region in one direction. A particular subfragment of the 1.3 kb IncM plasmid-derived DNA does not inhibit conjugation pilus expression at 30 degrees C but stimulates in trans the formation of pili at 42 degrees C to give rise to untypical sensitivity to phi M at 42 degrees C in addition to 30 degrees C. Other subfragments reveal vital interferences with IncM plasmid-harbouring host cells. The putative nature of the cloned determinants interfering with the normal expression of IncM plasmid DNA is discussed.
IncM质粒R446的一个1.3 kb DNA片段,如果克隆到多拷贝质粒中,会反式抑制携带IncM质粒的宿主细菌中接合菌毛的表达,这表现为它们对IncM菌毛依赖性噬菌体φM不敏感(Iml,对φM介导的裂解不敏感)。对该DNA片段的核苷酸序列进行测定、缺失的引入以及转座子插入的分析揭示了两个决定因素,即imlA和imlB,它们负责Iml表型。一段包含imlA的80 bp DNA和一段包含imlB的约450 bp相邻DNA共同作用,在30℃时抑制接合菌毛的典型表达。引入一个可转座的启动子探针并构建相应的lacZ融合体表明,互补链在体内的转录在包含imlA和imlB的区域重叠。此外,报告基因的表达揭示了imlA-imlB区域在一个方向上的温度依赖性转录。1.3 kb IncM质粒衍生DNA的一个特定亚片段在30℃时不抑制接合菌毛的表达,但在42℃时会反式刺激菌毛的形成,导致在30℃和42℃时对φM产生非典型敏感性。其他亚片段显示出对携带IncM质粒的宿主细胞有重要干扰。讨论了克隆的决定因素干扰IncM质粒DNA正常表达的假定性质。