Murphy M R, Fowlkes D M, Fitzgerald-Hayes M
Department of Biochemistry, University of Massachusetts, Amherst 01003.
Chromosoma. 1991 Dec;101(3):189-97. doi: 10.1007/BF00355368.
We constructed Saccharomyces cerevisiae centromere DNA mutants by annealing and ligating synthetic oligonucleotides, a novel approach to centromere DNA mutagenesis that allowed us to change only one structural parameter at a time. Using this method, we confirmed that CDE I, II, and III alone are sufficient for centromere function and that A + T-rich sequences in CDE II play important roles in mitosis and meiosis. Analysis of mutants also showed that a bend in the centromere DNA could be important for proper mitotic and meiotic chromosome segregation. In addition we demonstrated that the wild-type orientation of the CDE III sequence, but not the CDE I sequence, is critical for wild-type mitotic segregation. Surprisingly, we found that one mutant centromere affected the segregation of plasmids and chromosomes differently. The implications of these results for centromere function and chromosome structure are discussed.
我们通过退火和连接合成寡核苷酸构建了酿酒酵母着丝粒DNA突变体,这是一种着丝粒DNA诱变的新方法,使我们能够一次只改变一个结构参数。使用这种方法,我们证实单独的CDE I、II和III足以实现着丝粒功能,并且CDE II中富含A + T的序列在有丝分裂和减数分裂中起重要作用。对突变体的分析还表明,着丝粒DNA中的弯曲可能对正确的有丝分裂和减数分裂染色体分离很重要。此外,我们证明了CDE III序列的野生型方向而非CDE I序列的野生型方向对于野生型有丝分裂分离至关重要。令人惊讶的是,我们发现一个突变着丝粒对质粒和染色体的分离影响不同。讨论了这些结果对着丝粒功能和染色体结构的意义。