Hsu T, Wei R X, Dawson M, Karam J D
J Virol. 1987 Feb;61(2):366-74. doi: 10.1128/JVI.61.2.366-374.1987.
We have identified two bacteriophage T4 genes, 45.1 and 45.2, that map in the intergenic space between phage replication genes 46 (which encodes a recombination initiation protein) and 45 (which encodes a bifunctional protein required in replication and transcription). The existence of genes 45.1 and 45.2 had not been previously recognized by mutation analysis of the T4 genome. We cloned the T4 gene 45.1/45.2 segment, determined its nucleotide sequence, and expressed its two reading frames at high levels in bacterial plasmids. The results predicted molecular weights of 11,400 (100 amino acids) for gp45.1 and 7,500 (62 amino acids) for gp45.2. We also determined that in T4-infected Escherichia coli, genes 45.1 and 45.2 are cotranscribed with their distal neighbor, gene 45, by at least one mode of transcription. In an accompanying report (K. P. Williams, G. A. Kassavetis, F. S. Esch, and E. P. Geiduschek, J. Virol. 61:600-603, 1987), it is shown that the product of gene 45.1 is the so-called T4-induced 15K protein, an RNA polymerase-binding protein of unknown role in phage development. Possibly, T4 genes 45.2, 45.1, and 45 constitute an operon for host RNA polymerase-binding phage proteins. Jointly with Williams et al., we propose the term rpb (RNA polymerase-binding) to refer to T4 genes whose products bind to the host RNA polymerase and have adopted the name rpbA for T4 gene 45.1.
我们鉴定出了噬菌体T4的两个基因,45.1和45.2,它们定位于噬菌体复制基因46(编码一种重组起始蛋白)和45(编码复制和转录所需的双功能蛋白)之间的基因间隔区。通过对T4基因组的突变分析,此前尚未识别出基因45.1和45.2的存在。我们克隆了T4基因45.1/45.2片段,测定了其核苷酸序列,并在细菌质粒中高水平表达了其两个阅读框。结果预测gp45.1的分子量为11,400(100个氨基酸),gp45.2的分子量为7,500(62个氨基酸)。我们还确定,在T4感染的大肠杆菌中,基因45.1和45.2至少通过一种转录模式与其远端邻接基因45共转录。在一篇相关报道(K.P.威廉姆斯、G.A.卡萨韦蒂斯、F.S.埃施和E.P.盖杜谢克,《病毒学杂志》61:600 - 603,1987年)中表明,基因45.1的产物是所谓的T4诱导的15K蛋白,一种在噬菌体发育中作用未知的RNA聚合酶结合蛋白。可能,T4基因45.2、45.1和45构成了一个用于结合宿主RNA聚合酶的噬菌体蛋白的操纵子。我们与威廉姆斯等人共同提议用术语rpb(RNA聚合酶结合)来指代其产物与宿主RNA聚合酶结合的T4基因,并将T4基因45.1命名为rpbA。