Blaha Béla, Semsey Szabolcs, Ferenczi Szilamér, Csiszovszki Zsolt, Papp Péter P, Orosz László
Institute of Genetics, Agricultural Biotechnology Center, Gödöllõ, Szent-Györgyi A. 4., H-2100, Hungary.
Mol Microbiol. 2004 Nov;54(3):742-54. doi: 10.1111/j.1365-2958.2004.04300.x.
Several temperate bacteriophage utilize chromosomal sequences encoding putative tRNA genes for phage attachment. However, whether these sequences belong to genes which are functional as tRNA is generally not known. In this article, we demonstrate that the attachment site of temperate phage 16-3 (attB) nests within an active proline tRNA gene in Rhizobium meliloti 41. A loss-of-function mutation in this tRNA gene leads to significant delay in switching from lag to exponential growth phase. We converted the putative Rhizobium gene to an active amber suppressor gene which suppressed amber mutant alleles of genes of 16-3 phage and of Escherichia coli origin in R. meliloti 41 and in Agrobacterium tumefaciens GV2260. Upon lysogenization of R. meliloti by phage 16-3, the proline tRNA gene retained its structural and functional integrity. Aspects of the co-evolution of a temperate phage and its bacterium host is discussed. The side product of this work, i.e. construction of amber suppressor tRNA genes in Rhizobium and Agrobacterium, for the first time widens the options of genetic study.
几种温和噬菌体利用编码假定tRNA基因的染色体序列进行噬菌体附着。然而,这些序列是否属于具有tRNA功能的基因通常并不清楚。在本文中,我们证明了温和噬菌体16-3的附着位点(attB)位于苜蓿根瘤菌41中一个活跃的脯氨酸tRNA基因内。该tRNA基因的功能丧失突变导致从延滞期到指数生长期的转换显著延迟。我们将假定的根瘤菌基因转化为一个活跃的琥珀抑制基因,该基因在苜蓿根瘤菌41和根癌土壤杆菌GV2260中抑制了16-3噬菌体和大肠杆菌来源基因的琥珀突变等位基因。当噬菌体16-3使苜蓿根瘤菌溶源化时,脯氨酸tRNA基因保持其结构和功能完整性。本文还讨论了温和噬菌体与其细菌宿主的共同进化方面。这项工作的副产品,即在根瘤菌和土壤杆菌中构建琥珀抑制tRNA基因,首次拓宽了遗传学研究的选择范围。