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Efficient gene targeting in a Candida guilliermondii non-homologous end-joining pathway-deficient strain

机译:高效念珠菌假丝酵母非同源末端连接途径缺陷菌株中的基因靶向

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摘要

The yeast, Candida guilliermondii, has been widely studied due to its biotechnological interest as well as its biological control potential. It integrates foreign DNA predominantly via ectopic events, likely through the well-known non-homologous end-joining (NHEJ) pathway involving the Ku70p/Ku80p heterodimer, Lig4p, Nej1p and Lif1p. This phenomenon remains highly deleterious for targeted gene knock-out strategies that require the homologous recombination process. Here, we have constructed a ku70 mutant strain derived from the ATCC 6260 reference strain of C. guilliermondii. Following a series of disruption attempts of various genes (FCY1, ADE2 and TRP5), using several previously described dominant selectable markers (URA5, SAT-1 and HPH (#) ), we demonstrated that the efficiencies of homologous gene targeting in such a NHEJ-deficient strain was very high compared to the wild type strain. The C. guilliermondii ku70 deficient mutant thus represents a powerful recipient strain to knock-out genes efficiently in this yeast.
机译:由于其对生物技术的兴趣及其潜在的生物控制潜力,已广泛研究了古德念珠菌酵母。它主要通过异位事件整合外源DNA,可能是通过涉及Ku70p / Ku80p异二聚体,Lig4p,Nej1p和Lif1p的众所周知的非同源末端连接(NHEJ)途径进行的。对于需要同源重组过程的靶向基因敲除策略,该现象仍然非常有害。在这里,我们构建了一个来源于古氏梭状芽胞杆菌ATCC 6260参考菌株的ku70突变菌株。在使用几种先前描述的显性选择标记(URA5,SAT-1和HPH(#))对各种基因(FCY1,ADE2和TRP5)进行一系列破坏尝试之后,我们证明了在此类NHEJ中靶向同源基因的效率与野生型菌株相比,缺陷型菌株非常高。因此,C。guilliermondii ku70缺陷型突变体代表了强大的受体菌株,可以有效地敲除该酵母中的基因。

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