Wu H N, Lee J Y, Huang H W, Huang Y S, Hsueh T G
Institute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan, China.
Nucleic Acids Res. 1993 Sep 11;21(18):4193-9. doi: 10.1093/nar/21.18.4193.
We conducted extensive mutagenesis analysis on a hepatitis delta virus (HDV) genomic ribozyme to study the sequence specificity of certain region and to derive the secondary structure associated with the catalytic core. The results confirmed that the autocatalytic domain of HDV genomic RNA contained four base-pairing regions as predicted in the 'pseudo-knot' model [Perrotta & Been (1990) Nature 350, 434-436]. The size and sequence of one of the base-pairing regions, i. e. stem-and-loop, could be flexible. Helix 3 and the first basepair of helix 1 required specific sequence to retain self-cleavage activity. The structural requirement of helix 2 was less stringent than the other base-pairing regions. Moreover, the size of helix 1 affected self-cleavage whereas the length of hinge could be variable even though the first three residues of hinge had stringent sequence requirement.
我们对丁型肝炎病毒(HDV)基因组核酶进行了广泛的诱变分析,以研究特定区域的序列特异性,并推导与催化核心相关的二级结构。结果证实,HDV基因组RNA的自催化结构域包含四个碱基配对区域,正如“假结”模型[佩罗塔和贝恩(1990年)《自然》350, 434 - 436]中所预测的那样。其中一个碱基配对区域,即茎环结构的大小和序列可以是灵活的。螺旋3和螺旋1的第一个碱基对需要特定序列来保持自我切割活性。螺旋2的结构要求比其他碱基配对区域宽松。此外,螺旋1的大小影响自我切割,而铰链的长度可以变化,尽管铰链的前三个残基有严格的序列要求。