INRA, Micalis, UMR1319, 78350 Jouy-en-Josas, France.
Biotechnol Lett. 2013 Apr;35(4):571-6. doi: 10.1007/s10529-012-1107-0. Epub 2012 Dec 9.
In Yarrowia lipolytica, targeted gene replacement occurs only with long length (1 kb) homologous flanking fragments, as this yeast preferentially uses the non-homologous end-joining mechanism (NHEJ) for DNA repair over homologous recombination (HR). To improve the frequency of HR, we identified and disrupted the KU70 and KU80 genes responsible for double strand break repair in the NHEJ pathway in Y. lipolytica. In ku70∆ HR of URA3 marker at the ADE2 locus occurred with 43 % frequency with as little as 50 bp long flanking regions. The number of Ura(+) transformants was reduced to 1 % of the Po1d (ura3-302) wild type-like strain level, regardless of the flanking fragment length. On the contrary, even though HR was not improved in ku80∆, Ura(+) transformants was 60 % lower compared to the wild type.
在解脂耶氏酵母中,只有长长度(1 kb)的同源侧翼片段才能进行靶向基因替换,因为这种酵母在 DNA 修复中优先使用非同源末端连接机制(NHEJ)而非同源重组(HR)。为了提高 HR 的频率,我们鉴定并敲除了 KU70 和 KU80 基因,这些基因在 NHEJ 途径中负责双链断裂修复。在 ku70∆中,URA3 标记在 ADE2 基因座上的 HR 发生频率为 43%,侧翼区最短仅 50 bp。URA(+)转化体的数量减少到 Po1d(ura3-302)野生型样菌株水平的 1%,无论侧翼片段长度如何。相反,尽管 ku80∆中 HR 没有提高,但与野生型相比,URA(+)转化体的数量降低了 60%。