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Molecular characterization of KU70 and KU80 homologues and exploitation of a KU70-deficient mutant for improving gene deletion frequency in Rhodosporidium toruloides

机译:KU70和KU80同源物的分子表征和KU70缺陷型突变体的利用,以改善拟南芥假单胞菌的基因缺失频率

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Background Rhodosporidium toruloides is a β-carotenoid accumulating, oleaginous yeast that has great biotechnological potential. The lack of reliable and efficient genetic manipulation tools have been a major hurdle blocking its adoption as a biotechnology platform. Results We report for the first time the development of a highly efficient targeted gene deletion method in R. toruloides ATCC 10657 via Agrobacterium tumefaciens-mediated transformation. To further improve targeting frequency, the KU70 and KU80 homologs in R. toruloides were isolated and characterized in detail. A KU70-deficient mutant (?ku70e) generated with the hygromycin selection cassette removed by the Cre-loxP recombination system showed a dramatically improved targeted gene deletion frequency, with over 90% of the transformants being true knockouts when homology sequence length of at least 1?kb was used. Successful gene targeting could be made with homologous flanking sequences as short as 100?bp in the ?ku70e strain. KU70 deficiency did not perturb cell growth although an elevated sensitivity to DNA mutagenic agents was observed. Compared to the other well-known oleaginous yeast, Yarrowia lipolytica, R. toruloides KU70/KU80 genes contain much higher density of introns and are the most GC-rich KU70/KU80 genes reported. Conclusions The KU70-deficient mutant generated herein was effective in improving gene deletion frequency and allowed shorter homology sequences to be used for gene targeting. It retained the key oleaginous and fast growing features of R. toruloides. The strain should facilitate both fundamental and applied studies in this important yeast, with the approaches taken here likely to be applicable in other species in subphylum Pucciniomycotina.
机译:背景球形假单胞菌(Rhodosporidium toruloides)是一种具有丰富的生物技术潜力的β-类胡萝卜素积聚,含油酵母。缺乏可靠和有效的基因操作工具一直是阻碍其被用作生物技术平台的主要障碍。结果我们首次报道了通过根癌农杆菌介导的转化,在拟南芥ATCC 10657中高效靶向基因缺失方法的开发。为了进一步提高靶向频率,分离并详细表征了拟南芥中的KU70和KU80同源物。用Cre-loxP重组系统去除潮霉素选择盒后生成的KU70缺陷型突变体(?ku70e)显着提高了靶向基因的缺失频率,当同源序列长度至少为1时,超过90%的转化子是真正的敲除体使用?kb。成功的基因靶向可以通过在ku70e菌株中短至100 bp的同源侧翼序列完成。尽管观察到对DNA诱变剂的敏感性提高,但KU70缺乏症并未干扰细胞生长。与其他著名的产油酵母相比,解脂耶氏酵母(Yarrowia lipolytica),拟南芥R. toruloides KU70 / KU80基因含有更高的内含子密度,并且是报道的GC含量最高的KU70 / KU80基因。结论本文产生的KU70缺陷型突变体可有效地改善基因缺失频率,并允许较短的同源序列用于基因靶向。它保留了R. toruloides的主要油质性和快速生长的特征。该菌株应促进对该重要酵母的基础研究和应用研究,此处采用的方法可能适用于Pucciniomycotina亚种的其他物种。

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