Huang Z S, Ping Y H, Wu H N
Graduate Institute of Biotechnology, Chinese Culture University, Taipei, Taiwan.
FEBS Lett. 1997 Aug 18;413(2):299-303. doi: 10.1016/s0014-5793(97)00902-2.
A mutational analysis of the helix 3 (H3) region of hepatitis delta virus (HDV) ribozymes disclosed that an AU at the first base pair of H3 elevates the catalytic activity of various cis- and trans-acting HDV ribozymes. A GC to AU substitution at this position of H3, which is located at the junction of three of the four helices of the pseudoknot-like structure model, altered the structure of HDV ribozymes. This substitution in the H3 did not change the independence of the cleavage rate to pH nor the sensitivity to formamide treatment of the ribozymes.
对丁型肝炎病毒(HDV)核酶的螺旋3(H3)区域进行的突变分析表明,H3第一个碱基对处的AU可提高各种顺式和反式作用HDV核酶的催化活性。H3该位置(位于假结样结构模型四个螺旋中三个螺旋的交界处)的GC到AU替换改变了HDV核酶的结构。H3中的这种替换既未改变切割速率对pH的独立性,也未改变核酶对甲酰胺处理的敏感性。