Németh A H, Hunter N, Coleman M P, Borts R H, Louis E J, Davies K E
Molecular Genetics Group, John Radcliffe Hospital, Oxford, England.
Genet Anal Tech Appl. 1993;10(6):123-7. doi: 10.1016/1050-3862(93)90007-6.
During the construction of yeast artificial chromosome (YAC) libraries to facilitate mapping of the human genome, two YACs may be cotransformed into the same yeast cell, making further analysis very difficult. We present a simple method to rescue the required YAC that utilizes the segregation of chromosomes at meiosis. In brief, we crossed the cotransformed yeast cell with a non-YAC-containing strain and induced the resulting diploid to sporulate and undergo meiosis. The new haploid generation included some yeast cells that contained only the desired YAC. These YACs were analyzed by conventional methods. To exclude the possibility that major rearrangement occurred during the procedure, we analyzed the YACs with restriction enzymes that cut only rarely. We conclude that this is a useful technique to rescue cotransformed YACs.
在构建酵母人工染色体(YAC)文库以促进人类基因组图谱绘制的过程中,两个YAC可能会共转化到同一个酵母细胞中,这使得进一步分析变得非常困难。我们提出了一种简单的方法来拯救所需的YAC,该方法利用减数分裂时染色体的分离。简而言之,我们将共转化的酵母细胞与不含YAC的菌株杂交,并诱导产生的二倍体形成孢子并进行减数分裂。新的单倍体世代包括一些仅含有所需YAC的酵母细胞。这些YAC通过常规方法进行分析。为了排除在此过程中发生重大重排的可能性,我们用很少切割的限制酶分析了YAC。我们得出结论,这是一种拯救共转化YAC的有用技术。