Fukuda A, Sinsheimer R L
J Virol. 1976 Apr;18(1):218-26. doi: 10.1128/JVI.18.1.218-226.1976.
Mutation in several different cistrons of bacteriophage phi chi 174 blocks net progeny single-stranded DNA synthesis at the late period of infection (15). For the study of the functions of these cistrons in single-stranded DNA synthesis, asymmetric replication of replicative form DNA was examined at the late period of infection with amber mutants of these cistrons. While the normal, rapid process of asymmetric single-stranded viral DNA synthesis is blocked at the late period of these mutant infections, an asymmetric synthesis of the viral strand of replicative-form DNA is observed in this period, though at a reduced level, together with degradation of prelabeled viral strand. Some intermediate replicative-form molecules were also detected. Asymmetric synthesis of the viral strand of replicative-form DNA at the late period of phi chi infection is completely inhibited in the presence of a low concentration (35mug/ml) of chloramphenicol (which also blocks net single-stranded viral DNA synthesis). These results are discussed in terms of the possible role of the specific viral proteins for normal single-stranded DNA synthesis.
噬菌体φX174几个不同顺反子中的突变会在感染后期阻断子代单链DNA的净合成(15)。为了研究这些顺反子在单链DNA合成中的功能,在这些顺反子的琥珀突变体感染后期,检测了复制型DNA的不对称复制。虽然在这些突变体感染后期,正常、快速的不对称单链病毒DNA合成过程被阻断,但在此期间仍可观察到复制型DNA病毒链的不对称合成,不过水平有所降低,同时预标记的病毒链会发生降解。还检测到了一些中间复制型分子。在低浓度(35μg/ml)氯霉素存在的情况下(氯霉素也会阻断单链病毒DNA的净合成),φX感染后期复制型DNA病毒链的不对称合成被完全抑制。根据特定病毒蛋白在正常单链DNA合成中可能发挥的作用对这些结果进行了讨论。