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通过对188个cDNA克隆进行序列分析得出的具有八个新接触点的丁型肝炎病毒反基因组核酶的三维模型。

3-D models of the antigenomic ribozyme of the hepatitis delta agent with eight new contacts suggested by sequence analysis of 188 cDNA clones.

作者信息

Branch A D, Polaskova J A

机构信息

Department of Medicine, Mount Sinai Medical Center, New York, NY 10029, USA.

出版信息

Nucleic Acids Res. 1995 Oct 25;23(20):4180-9. doi: 10.1093/nar/23.20.4180.

Abstract

We mapped 359 mutations at 25 positions in synthetic variants of the antigenomic ribozyme of the hepatitis delta agent by analyzing the sequences of 188 cDNA clones. These data were used to identify three features of the ribozyme: highly conserved nucleotides, positions with restricted nucleotide substitutions and three-dimensional relationships between nucleotides. The distribution of mutations at the 25 positions was as follows: G-11 (the eleventh nucleotide from the cleavage site) was mutated in 56 clones; G-12 in 36; U-15 in 33; C-13 in 26; G-28 in 23; C-27 in 21; C-29 in 19; U-26 in 17; C-18 in 14; A-14 in 13; C-16 in 13; C-19 in 12; U-17 in 11; A-20 in 10; G-42 in 9; G-40 in 7; G-41 in 7; C-24 in 6; U-32 in 6; U-23 in 5; C-25 in 4; C-21 in 3; G-30 in 3; G-31 in 3; C-22 in 1. All clones containing a mutation at C-25 had an A at this position, suggesting that the extra cyclic amino group present in adenine and cytosine may function during the cleavage event. Mutations at certain positions were common in simple clones (containing only one or two mutations), while mutations at other positions were over-represented in more complex clones. Both compensatory base changes and co-mutational frequencies were used to identify eight pairs of nucleotides which may interact with each other: G-11 and C-18, G-12 and C-27, C-13 and G-28, C-21 and U-23/C-24, C-21 and G-30, U-23 and G-31/U-32, C24 and G-30, C-27 and G-42. These pairs, which involve some of the most conserved positions in the molecule, suggest interactions among nucleotides previously depicted in open-loop structures. The newly proposed points of contact between pairs of nucleotides are compatible with both the axehead and pseudoknot secondary structural models and were combined with previously proposed Watson-Crick base paired helices to produce two three dimensional models. In both of these, C-25 and C-76 are placed near the cleavage site.

摘要

我们通过分析188个cDNA克隆的序列,绘制了丁型肝炎病毒反基因组核酶合成变体中25个位置的359个突变图谱。这些数据用于确定核酶的三个特征:高度保守的核苷酸、核苷酸替代受限的位置以及核苷酸之间的三维关系。25个位置的突变分布如下:G-11(切割位点起第11个核苷酸)在56个克隆中发生突变;G-12在36个中;U-15在33个中;C-13在26个中;G-28在23个中;C-27在21个中;C-29在19个中;U-26在17个中;C-18在14个中;A-14在13个中;C-16在13个中;C-19在12个中;U-17在11个中;A-20在10个中;G-42在9个中;G-40在7个中;G-41在7个中;C-24在6个中;U-32在6个中;U-23在5个中;C-25在4个中;C-21在3个中;G-30在3个中;G-31在3个中;C-22在1个中。所有在C-25处有突变的克隆在该位置都有一个A,这表明腺嘌呤和胞嘧啶中存在的额外环氨基可能在切割事件中起作用。某些位置的突变在简单克隆(仅含一两个突变)中很常见,而其他位置的突变在更复杂的克隆中出现频率过高。补偿性碱基变化和共突变频率都用于确定可能相互作用的八对核苷酸:G-11和C-18、G-12和C-27、C-13和G-28、C-21和U-23/C-24、C-21和G-30、U-23和G-31/U-32、C24和G-30、C-27和G-42。这些涉及分子中一些最保守位置的配对表明了先前在开环结构中描绘的核苷酸之间的相互作用。新提出的核苷酸对之间的接触点与斧头状和假结二级结构模型都兼容,并与先前提出的沃森-克里克碱基配对螺旋相结合,产生了两个三维模型。在这两个模型中,C-25和C-76都位于切割位点附近。

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