[Genetic system for maintaining the mitochondrial human genome in yeast Yarrowia lipolytica].

E P Isakova, Yu I Deryabina, A V Velyakova, J K Biryukova, V V Teplova, A B Shevelev
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Abstract

For the first time, the possibility of maintaining an intact human mitochondrial genome in a heterologous system in the mitochondria of yeast Yarrowia lipolytica is shown. A method for introducing directional changes into the structure of the mitochondrial human genome replicating in Y. lipolytica by an artificially induced ability of yeast mitochondria for homologous recombination is proposed. A method of introducing and using phenotypic selection markers for the presence or absence of defects in genes tRNA-Lys and tRNA-Leu of the mitochondrial genome is developed. The proposed system can be used to correct harmful mutations of the human mitochondrial genome associated with mitochondrial diseases and for preparative amplification of intact mitochondrial DNA with an adjusted sequence in yeast cells. The applicability of the new system for the correction of mutations in the genes of Lys- and Leu-specific tRNAs of the human mitochondrial genome associated with serious and widespread human mitochondrial diseases such as myoclonic epilepsy with lactic acidosis (MELAS) and myoclonic epilepsy with ragged-red fibers (MERRF) is shown.

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[酵母多脂耶氏菌维持线粒体人类基因组的遗传系统]。
这是第一次,在酵母多脂耶氏菌线粒体的异源系统中维持完整的人类线粒体基因组的可能性。提出了一种通过人工诱导酵母线粒体同源重组能力来引入定向改变人类线粒体基因组结构的方法。提出了一种引入和使用线粒体基因组tRNA-Lys和tRNA-Leu基因存在或不存在缺陷的表型选择标记的方法。所提出的系统可用于纠正与线粒体疾病相关的人类线粒体基因组的有害突变,并用于酵母细胞中具有调整序列的完整线粒体DNA的准备扩增。该新系统可用于校正与严重和广泛的人类线粒体疾病(如肌阵挛性癫痫伴乳酸酸中毒(MELAS)和肌阵挛性癫痫伴红肌纤维(MERRF))相关的人类线粒体基因组中Lys和leu特异性trna基因突变。
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