Nobile C, Martin R G
Intervirology. 1986;25(3):158-71. doi: 10.1159/000149671.
With the objective of generating DNA molecules that form stable stem-loop structures or cruciform structures in solution, we have altered the palindromic sequence at the Simian Virus 40 (SV40) replication origin. These alterations include: deletion of 18 of the 27 base pairs (bp) in the 13-bp inverted repeat; deletion of 26 of the 27 bp; substitution of the entire 27 bp with a totally different 26-bp sequence containing a 13-bp inverted repeat; and substitution of the 27 bp with an 8-bp sequence containing a 4-bp inverted repeat. The DNA from these mutants was purified. Mutant DNAs were hybridized to wild-type SV40 DNA or to each other, and the heteroduplexes were purified. The predicted structures were verified by S1 and restriction endonuclease digestion. The mutants - the heteroduplexes have not been tested - are capable of complementing tsA mutants and/or transforming mouse cells.
为了生成能在溶液中形成稳定茎环结构或十字形结构的DNA分子,我们改变了猴病毒40(SV40)复制起点处的回文序列。这些改变包括:在13个碱基对的反向重复序列中删除27个碱基对(bp)中的18个;删除27个bp中的26个;用包含13个bp反向重复序列的完全不同的26个bp序列替换整个27个bp;以及用包含4个bp反向重复序列的8个bp序列替换27个bp。从这些突变体中纯化出DNA。将突变体DNA与野生型SV40 DNA或彼此杂交,并纯化异源双链体。通过S1核酸酶和限制性内切酶消化验证了预测的结构。这些突变体——尚未对异源双链体进行测试——能够互补tsA突变体和/或转化小鼠细胞。