Center M S
J Virol. 1975 Jul;16(1):94-100. doi: 10.1128/JVI.16.1.94-100.1975.
Studies have been carried out to elucidate the in vivo function of gene 2 in T7 DNA synthesis. In gene 2-infected cells the rate of incorporation of (3-H)thymidine into acid-insoluble material is about 60% that of cells infected with T7 wild type. Gene 2 mutants do not however produce viable phage after infection of the nonpermissive host. In T7 wild type-infected cells, a major portion of the newly alkaline sucrose gradients. The concatemers serve as precursors for the formation of mature T7 DNA as demonstrated in pulse-chase experiments. In similar studies carried out with gene 2-infected cells, concatemers are not detected when the intracellular DNA is analyzed at several different times during the infection process. The DNA made during a gene 2 infection is present as duplex structures with a sedimentation rate close to mature T7 DNA.
已经开展了多项研究来阐明基因2在T7 DNA合成中的体内功能。在感染了基因2的细胞中,(3-H)胸腺嘧啶核苷掺入酸不溶性物质的速率约为感染T7野生型细胞的60%。然而,基因2突变体在感染非允许宿主后不会产生有活力的噬菌体。在感染T7野生型的细胞中,新合成的DNA大部分以串联体形式存在于碱性蔗糖梯度中。如脉冲追踪实验所示,串联体是成熟T7 DNA形成的前体。在用感染了基因2的细胞进行的类似研究中,在感染过程中的几个不同时间分析细胞内DNA时未检测到串联体。基因2感染过程中产生的DNA以双链结构形式存在,沉降速率接近成熟T7 DNA。