Hiasa H, Tanaka K, Sakai H, Yoshida K, Honda Y, Komano T, Godson G N
Department of Agricultural Chemistry, Kyoto University, Japan.
Gene. 1989 Dec 7;84(1):17-22. doi: 10.1016/0378-1119(89)90134-0.
Three potential secondary structures, stem-loops I, II, and III, are contained in the phage G4 origin of complementary DNA strand synthesis, G4oric, and are believed to be involved in its recognition by dnaG-encoded primase and the synthesis of primer RNA. In a previous publication [Sakai et al., Gene 71 (1988) 323-330], we suggested that base pairing between the loops of stem-loops I, and II, and/or II and III, might play a role in G4oric function. To test this hypothesis, site-directed mutagenesis was used to construct mutants which carried base substitutions in loops I, II and III that destroyed possible interloop base pairing. These mutations, however, did not seriously affect G4oric activity. This indicates that base pairing between the loops is not essential for G4oric functional activity, and also that base substitutions which do not affect the secondary structure of stem-loops I, II and III, do not affect G4oric activity. To complete an analysis of the effects of altering the structure of the G4oric stem-loops, insertions were made into stem-loop III. In contrast to stem-loops I and II, all insertions into stem-loop III destroyed in vivo G4oric activity.
噬菌体G4互补DNA链合成起点G4oric中包含三种潜在的二级结构,即茎环I、II和III,据信它们参与了dnaG编码的引发酶对其的识别以及引物RNA的合成。在之前的一篇论文中[Sakai等人,《基因》71(1988)323 - 330],我们提出茎环I与II的环之间和/或II与III的环之间的碱基配对可能在G4oric功能中发挥作用。为了验证这一假设,我们使用定点诱变构建了一些突变体,这些突变体在环I、II和III中携带碱基替换,破坏了可能的环间碱基配对。然而,这些突变并没有严重影响G4oric的活性。这表明环间的碱基配对对于G4oric的功能活性不是必需的,并且不影响茎环I、II和III二级结构的碱基替换也不会影响G4oric的活性。为了全面分析改变G4oric茎环结构的影响,我们在茎环III中进行了插入操作。与茎环I和II不同,所有插入茎环III的操作都破坏了G4oric在体内的活性。