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Structure-function relationships in a self-splicing group II intron: a large part of domain II of the mitochondrial intron al5 is not essential for self-splicing

机译:自剪接组II内含子中的结构-功能关系:线粒体内含子al5的大部分结构域II对于自剪接不是必需的

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An oligonucleotide-directed deletion of 156 nucleotides has been introduced into the yeast mitochondrial group II intron al5 (887 nt). The deletion comprises almost all of domain II, which is one of the six phylogenetically conserved structural elements of group II introns. This mutant displays reduced self-splicing activity, but results of chemical probing with dimethylsulphate suggest that sequences at the site of the deletion interfere with the normal folding of the intron. This is supported by computer analyses, which predict a number of alternative structures involving conserved intron sequences. Splicing activity could be restored by insertion of a 10-nucleotide palindromic sequence into the unique Smal site of the deletion mutant, resulting in the formation of a small stable stem-loop element at the position of domain II. These results provide a direct correlation between folding of the RNA and its activity. We conclude that at least a large part of domain II of the group II intron al5 is not required for self-splicing activity. This deletion mutant with a length of 731 nucleotides represents the smallest self-splicing group II intron so far known.
机译:寡核苷酸定向的156个核苷酸的缺失已被引入酵母线粒体II组内含子al5(887 nt)。该缺失几乎包含结构域II的全部,该结构域II是组II内含子的六个系统进化上保守的结构元件之一。该突变体显示降低的自剪接活性,但是用硫酸二甲酯进行化学探测的结果表明,缺失位点的序列干扰内含子的正常折叠。这由计算机分析支持,该计算机分析预测了涉及保守内含子序列的许多替代结构。剪接活性可以通过将10个核苷酸的回文序列插入缺失突变体的独特Smal位点来恢复,从而在结构域II的位置形成一个小的稳定茎环元件。这些结果提供了RNA折叠与其活性之间的直接关联。我们得出结论,II型内含子al5的结构域II的至少很大一部分对于自我剪接活性不是必需的。长度为731个核苷酸的这种缺失突变体代表了迄今为止已知的最小的自我剪接的II组内含子。

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