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Intron 5α of the COXI gene of yeast mitochondrial DNA is a mobile group I intron

机译:酵母线粒体DNA COXI基因的内含子5α是可移动的I组内含子

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We have found that intron 5a of the COXI gene (al5α) of yeast mtDNA is a mobile group I intron in crosses between strains having or lacking the Intron. We have demonstrated the following hallmarks of that process: 1) co-conversion of flanking optional intron markers; 2) mutations that truncate the intron open reading frame block intron mobility; and 3) the intron open reading frame encodes an endonuclease activity that is required for intron movement. The endonuclease activity, termed I-Sce IV, cleaves the COXI allele lacking al5a near the site of intron insertion, making a four-base staggered cut with 3' OH overhangs. Three cloned DNAs derived from different forms of the COXI gene, which differ In primary sequence at up to seven nucleotides around the cleavage site, are all good substrates for In vitro I-Sce IV cleavage activity. Two of the strains from which these substrates were derived were tested in crosses and are comparably efficient as al5a recipients. When compared with w mobility occurring simultaneously in one cross, al5a is less efficient as a mobile element.
机译:我们已经发现,酵母mtDNA的COXI基因(al5α)的内含子5a在具有或缺乏内含子的菌株之间的杂交中是可移动的I组内含子。我们已经证明了该过程的以下标志:1)侧翼可选内含子标记的共转化; 2)截短内含子开放阅读框的突变阻止了内含子的迁移; 3)内含子开放阅读框编码内含子移动所需的核酸内切酶活性。称为I-Sce IV的核酸内切酶活性可在内含子插入位点附近切割缺少al5a的COXI等位基因,从而形成一个4碱基交错的3'OH突出端的切口。源自COXI基因不同形式的三个克隆DNA在切割位点周围多达七个核苷酸的一级序列不同,它们都是体外I-Sce IV切割活性的良好底物。杂交测试了衍生出这些底物的两种菌株,它们作为al5a受体具有相当的效率。当与在一个十字路口同时发生的移动性比较时,al5a作为移动元件的效率较低。

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