Liu Li, Cheng Shuqiu, van Brabant Anja J, Kmiec Eric B
Department of Biology, Delaware Biotechnology Institute, University of Delaware, 15 Innovation Way, Room 270, Newark, DE 19711, USA.
Nucleic Acids Res. 2002 Jul 1;30(13):2742-50. doi: 10.1093/nar/gkf397.
Synthetic single-stranded DNA vectors have been used to correct point and frameshift mutations in episomal or chromosomal targets in the yeast Saccharomyces cerevisiae. Certain parameters, such as the length of the vector and the genetic background of the organism, have a significant impact on the process of targeted gene repair, and point mutations are corrected at a higher frequency than frameshift mutations. Genetic analyses reveal that expression levels of the recombination/repair genes RAD51, RAD52 and RAD54 can affect the frequency of gene repair. Overexpression of RAD51 enhances the frequency 4-fold for correction of an episomal target and 5-fold for correction of a chromosomal target; overexpression of RAD54 is also effective in stimulating gene repair, to the same extent as RAD51 in the chromosomal target. In sharp contrast, RAD52 gene expression serves to reduce gene repair activity in rescue experiments and in experiments where RAD52 is overexpressed in a wild-type strain. This may suggest an antagonist role for Rad52p. Consistent with this notion, the highest level of targeted repair occurs when the RAD51 gene is overexpressed in a strain of yeast deficient in RAD52 gene function.
合成单链DNA载体已被用于纠正酿酒酵母中游离型或染色体靶标的点突变和移码突变。某些参数,如载体长度和生物体的遗传背景,对靶向基因修复过程有显著影响,且点突变的校正频率高于移码突变。遗传分析表明,重组/修复基因RAD51、RAD52和RAD54的表达水平会影响基因修复频率。RAD51的过表达使游离型靶标的校正频率提高4倍,使染色体靶标的校正频率提高5倍;RAD54的过表达在刺激基因修复方面也有效,在染色体靶标中与RAD51的效果相同。形成鲜明对比的是,在拯救实验以及在野生型菌株中过表达RAD52的实验中,RAD52基因表达会降低基因修复活性。这可能表明Rad52p具有拮抗作用。与此观点一致的是,当在缺乏RAD52基因功能的酵母菌株中过表达RAD51基因时,靶向修复水平最高。