Inokuchi Y, Hirashima A
Department of Molecular Biology, School of Medicine, Keio University, Tokyo, Japan.
J Virol. 1987 Dec;61(12):3946-9. doi: 10.1128/JVI.61.12.3946-3949.1987.
RNA-dependent RNA and DNA polymerases have a conserved segment, Tyr-X-Asp-Asp (G. Karmer and P. Argos, Nucleic Acids Res. 12:7269-7282, 1984). To investigate the function of this segment, we changed the Gly residue at position 357 in the conserved sequence Tyr-356-Gly-357-Asp-358-Asp-359 of the replicase of RNA coliphage Q beta to Ala, Ser, Pro, Met, or Val and examined the replicase activity in vivo. Cells carrying the variant plasmids lost the replicase activity and severely inhibited the proliferation of phage Q beta (group III) and related phage SP (group IV) by suppressing phage RNA synthesis. In contrast, substitution of the Gly residue at 390 showed only a slight inhibitory effect, although replicase activity was also lost. These results suggest that the cells harboring an altered replicase at the conserved segment can interfere specifically with the wild-type phage and different but related phage infections.
依赖RNA的RNA和DNA聚合酶有一个保守片段,即酪氨酸- X -天冬氨酸-天冬氨酸(G. 卡默和P. 阿戈斯,《核酸研究》12:7269 - 7282,1984年)。为了研究该片段的功能,我们将RNA噬菌体Qβ复制酶保守序列酪氨酸- 356 -甘氨酸- 357 -天冬氨酸- 358 -天冬氨酸- 359中第357位的甘氨酸残基分别替换为丙氨酸、丝氨酸、脯氨酸、甲硫氨酸或缬氨酸,并在体内检测复制酶活性。携带变异质粒的细胞失去了复制酶活性,并通过抑制噬菌体RNA合成严重抑制了噬菌体Qβ(III组)和相关噬菌体SP(IV组)的增殖。相比之下,第390位甘氨酸残基的替换虽然也使复制酶活性丧失,但仅表现出轻微的抑制作用。这些结果表明,在保守片段处具有改变的复制酶的细胞可以特异性地干扰野生型噬菌体以及不同但相关的噬菌体感染。