Dobbins Aleisha T, George Matthew, Basham Daryl A, Ford Michael E, Houtz Jennifer M, Pedulla Marisa L, Lawrence Jeffrey G, Hatfull Graham F, Hendrix Roger W
Department of Biochemistry and Molecular Biology, Howard University College of Medicine, Washington, DC 20059, USA.
J Bacteriol. 2004 Apr;186(7):1933-44. doi: 10.1128/JB.186.7.1933-1944.2004.
We report the complete genome sequence of enterobacteriophage SP6, which infects Salmonella enterica serovar Typhimurium. The genome contains 43,769 bp, including a 174-bp direct terminal repeat. The gene content and organization clearly place SP6 in the coliphage T7 group of phages, but there is approximately 5 kb at the right end of the genome that is not present in other members of the group, and the homologues of T7 genes 1.3 through 3 appear to have undergone an unusual reorganization. Sequence analysis identified 10 putative promoters for the SP6-encoded RNA polymerase and seven putative rho-independent terminators. The terminator following the gene encoding the major capsid subunit has a termination efficiency of about 50% with the SP6-encoded RNA polymerase. Phylogenetic analysis of phages related to SP6 provided clear evidence for horizontal exchange of sequences in the ancestry of these phages and clearly demarcated exchange boundaries; one of the recombination joints lies within the coding region for a phage exonuclease. Bioinformatic analysis of the SP6 sequence strongly suggested that DNA replication occurs in large part through a bidirectional mechanism, possibly with circular intermediates.
我们报道了感染肠炎沙门氏菌鼠伤寒血清型的肠道噬菌体SP6的全基因组序列。该基因组包含43,769个碱基对,包括一个174个碱基对的直接末端重复序列。基因内容和组织明确将SP6归为噬菌体T7噬菌体群,但基因组右端约有5 kb在该群的其他成员中不存在,并且T7基因1.3至3的同源物似乎经历了异常的重组。序列分析确定了10个SP6编码的RNA聚合酶的推定启动子和7个推定的不依赖rho的终止子。编码主要衣壳亚基的基因之后的终止子,在SP6编码的RNA聚合酶作用下终止效率约为50%。对与SP6相关的噬菌体进行系统发育分析,为这些噬菌体谱系中的序列水平交换提供了明确证据,并清晰划定了交换边界;其中一个重组接头位于噬菌体核酸外切酶的编码区内。对SP6序列的生物信息学分析强烈表明,DNA复制很大程度上通过双向机制进行,可能存在环状中间体。