Mitrikeski Petar Tomev
Laboratory for Evolutionary Genetics, Division of Molecular Biology, Ruđer Bošković Institute, Bijenička cesta 54, 10000, Zagreb, Croatia.
Faculty of Philosophy and Religious Studies, University of Zagreb, Jordanovac 110, PO Box 169, 10000, Zagreb, Croatia.
Curr Genet. 2022 Dec;68(5-6):551-564. doi: 10.1007/s00294-022-01246-y. Epub 2022 Jul 6.
Gene-targeting is one of the most important molecular tools for genomic manipulations for research and industrial purposes. However, many factors influence targeting fidelity undermining the efforts for accurate, fast, and reliable construction of genetically modified yeast strains. Therefore, it is of great academic interest that we uncover as many as possible parameters affecting the recombination mechanisms that enable targeting. Since usually, researchers choose the orientation of the insertion (marker) within the module at random, it seemed interesting to see whether the same module will achieve essentially the same targeting efficiency when the same marker was oriented alternatively concerning the same target gene. Thus, two loci (URA3 and LEU2) and one allele (ura3-52) in a haploid yeast genetic background were targeted by artificial modules bearing homologous insertions in alternative orientations being flanked by long asymmetrical targeting homology to either replace or disrupt a genomic target. Results showed that insertion orientation within the targeting module strongly influences targeting in yeast, regardless of the targeting approach.
基因靶向是用于研究和工业目的的基因组操作最重要的分子工具之一。然而,许多因素会影响靶向保真度,破坏准确、快速和可靠构建转基因酵母菌株的努力。因此,尽可能多地揭示影响实现靶向的重组机制的参数具有重大的学术意义。由于通常研究人员会随机选择模块内插入(标记)的方向,所以看看当相同标记相对于相同靶基因以相反方向排列时,同一个模块是否会实现基本相同的靶向效率似乎很有意思。因此,在单倍体酵母遗传背景下的两个基因座(URA3和LEU2)和一个等位基因(ura3-52)被人工模块靶向,这些模块带有以相反方向排列的同源插入片段,两侧是长的不对称靶向同源序列,用于替换或破坏基因组靶标。结果表明,无论靶向方法如何,靶向模块内的插入方向都会强烈影响酵母中的靶向作用。