Fairhead C, Dujon B
Unité de Génétique moléculaire des Levures (URA 1149 du CNRS), Institut Pasteur, Paris, France.
Mol Gen Genet. 1993 Aug;240(2):170-8. doi: 10.1007/BF00277054.
We have developed a system in which a unique double-stranded break (DSB) can be introduced into a yeast chromosome during mitotic growth. The recognition site for the endonuclease I-SceI was inserted at different places in the yeast genome in haploid and diploid cells expressing this endonuclease. Induction of the break in haploids results in cell death if no intact copy of the cleaved region is present in the cell. If such a copy is provided on a plasmid, as an ectopic gene duplication, or on a homologous chromosome, the break can be repaired. Repair results in two identical copies in the genome of the locus which has been cut. We call this phenomenon homozygotization by reference to diploids heterozygous for the cut site in which repair leads to homozygosis at this site. We have compared the efficiencies of repair in the various topological situations examined, and conclude that some mechanism must search for regions of homology to both sides of the DSB and that repair is successful only if the homologies are provided by the same template molecule.
我们开发了一种系统,在有丝分裂生长过程中可将独特的双链断裂(DSB)引入酵母染色体。在表达内切核酸酶I-SceI的单倍体和二倍体细胞中,将该内切核酸酶的识别位点插入酵母基因组的不同位置。如果细胞中不存在切割区域的完整拷贝,单倍体中诱导断裂会导致细胞死亡。如果通过异位基因复制在质粒上或在同源染色体上提供这样的拷贝,则可以修复断裂。修复导致在已切割位点的基因组中产生两个相同的拷贝。参考在切割位点为杂合子的二倍体,其中修复导致该位点纯合化,我们将这种现象称为纯合化。我们比较了所研究的各种拓扑情况下的修复效率,并得出结论,一定存在某种机制来搜索DSB两侧的同源区域,并且只有当同源性由同一模板分子提供时修复才会成功。