Koshland D, Kent J C, Hartwell L H
Cell. 1985 Feb;40(2):393-403. doi: 10.1016/0092-8674(85)90153-9.
The fidelity of the mitotic transmission of minichromosomes in S. cerevisiae is monitored by a novel visual assay that allows one to detect changes in plasmid copy number in individual mitotic divisions. This assay is used to investigate the mitotic transmission of a plasmid containing a putative yeast origin of replication (ARS 1) and a centromere (CEN3). The rate of improper segregation for the minichromosome is 200-fold higher than observed for a normal chromosome. However, the replication of the minichromosome is stringently controlled; it overreplicates less than once per one thousand mitotic divisions. We also use this assay to isolate and characterize mutations in ARS 1 and CEN3. The mutations in ARS 1 define a new domain required for its optimal activity, and the mutations in CEN3 suggest that the integrity of element II is not essential for centromere function. Finally, the phenotypes of the mutations in ARS 1 and CEN3 are consistent with their function in replication and segregation, respectively.
通过一种新颖的视觉检测方法来监测酿酒酵母中微型染色体有丝分裂传递的保真度,该方法能够让人们检测单个有丝分裂过程中质粒拷贝数的变化。此检测方法用于研究含有假定酵母复制起点(ARS 1)和着丝粒(CEN3)的质粒的有丝分裂传递。微型染色体的错误分离率比正常染色体高出200倍。然而,微型染色体的复制受到严格控制;每一千次有丝分裂中其过度复制少于一次。我们还利用该检测方法来分离和鉴定ARS 1和CEN3中的突变。ARS 1中的突变定义了其最佳活性所需的一个新结构域,而CEN3中的突变表明元件II的完整性对于着丝粒功能并非必不可少。最后,ARS 1和CEN3中突变的表型分别与其在复制和分离中的功能一致。