Casjens Sherwood R, Gilcrease Eddie B, Huang Wai Mun, Bunny Kim L, Pedulla Marisa L, Ford Michael E, Houtz Jennifer M, Hatfull Graham F, Hendrix Roger W
Department of Pathology, University of Utah Medical School, Salt Lake City, Utah 84132, USA.
J Bacteriol. 2004 Mar;186(6):1818-32. doi: 10.1128/JB.186.6.1818-1832.2004.
Temperate bacteriophages with plasmid prophages are uncommon in nature, and of these only phages N15 and PY54 are known to have a linear plasmid prophage with closed hairpin telomeres. We report here the complete nucleotide sequence of the 51,601-bp Klebsiella oxytoca linear plasmid pKO2, and we demonstrate experimentally that it is also a prophage. We call this bacteriophage phiKO2. An analysis of the 64 predicted phiKO2 genes indicate that it is a fairly close relative of phage N15; they share a mosaic relationship that is typical of different members of double-stranded DNA tailed-phage groups. Although the head, tail shaft, and lysis genes are not recognizably homologous between these phages, other genes such as the plasmid partitioning, replicase, prophage repressor, and protelomerase genes (and their putative targets) are so similar that we predict that they must have nearly identical DNA binding specificities. The phiKO2 virion is unusual in that its phage lambda-like tails have an exceptionally long (3,433 amino acids) central tip tail fiber protein. The phiKO2 genome also carries putative homologues of bacterial dinI and umuD genes, both of which are involved in the host SOS response. We show that these divergently transcribed genes are regulated by LexA protein binding to a single target site that overlaps both promoters.
带有质粒原噬菌体的温和噬菌体在自然界中并不常见,在这些噬菌体中,只有N15和PY54噬菌体已知具有带有封闭发夹端粒的线性质粒原噬菌体。我们在此报告了产酸克雷伯菌线性质粒pKO2的51,601 bp完整核苷酸序列,并通过实验证明它也是一种原噬菌体。我们将这种噬菌体称为phiKO2。对64个预测的phiKO2基因的分析表明,它是噬菌体N15的相当近的亲缘种;它们具有双链DNA尾噬菌体组不同成员典型的镶嵌关系。尽管这些噬菌体之间的头部、尾轴和裂解基因没有明显的同源性,但其他基因,如质粒分配、复制酶、原噬菌体阻遏物和原端粒酶基因(及其假定靶点)非常相似,以至于我们预测它们必须具有几乎相同的DNA结合特异性。phiKO2病毒粒子不同寻常之处在于其类似噬菌体λ的尾部有一个异常长(3433个氨基酸)的中央末端尾纤维蛋白。phiKO2基因组还携带细菌dinI和umuD基因的假定同源物,这两个基因都参与宿主的SOS反应。我们表明,这些反向转录的基因受LexA蛋白与一个重叠两个启动子的单一靶位点结合的调控。