Department of Radiation Biology and Biophysics, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642.
Genetics. 1983 Mar;103(3):367-88. doi: 10.1093/genetics/103.3.367.
Revertants of the cyc1-512 transcription termination mutant of the yeast Saccharomyces cerevisiae were isolated and subjected to a detailed genetic analysis. The cyc1-512 mutation previously was shown to be a 38-base pair deletion that causes only 10% of the normal steady-state levels of CYC1 mRNA and of the CYC1 gene product, iso-1-cytochrome c. Forty-one cyc1-512 revertants were classified by their content of iso-1-cytochrome c and by their genetic properties in meiotic crosses. Many of the revertants contain local genetic changes that either partially or completely restore the level of iso-1-cytochrome c. One revertant was shown to contain an unlinked extragenic suppressor, designated sut1, that causes partial suppression of the transcription termination defect. Four revertants of cyc1-512 contain chromosomal rearrangements with breakpoints that are tightly linked to the CYC1 locus; these include one duplication, one possible inversion, and two reciprocal translocations. Detailed genetic mapping demonstrated that one of the reciprocal translocations is between the right arms of chromosomes X and XII, with a breakpoint mapping 3' to the CYC1 locus. These results indicate that the defect in transcription termination in cyc1-512 can be restored in a variety of ways, including the translocation of different chromosomal regions to the 3' end of the CYC1 locus, local changes presumably at or near the original defect, and by mutation at another locus distinct from CYC1.
酵母酿酒酵母 cyc1-512 转录终止突变体的回复突变体被分离出来,并进行了详细的遗传分析。cyc1-512 突变先前被证明是一个 38 个碱基对的缺失,导致 CYC1 mRNA 和 CYC1 基因产物 iso-1-细胞色素 c 的正常稳态水平仅为 10%。41 个 cyc1-512 回复突变体根据其 iso-1-细胞色素 c 的含量和减数分裂交叉中的遗传特性进行分类。许多回复突变体包含局部遗传变化,这些变化部分或完全恢复了 iso-1-细胞色素 c 的水平。一个回复突变体被证明含有一个不连锁的外基因抑制子,命名为 sut1,它导致转录终止缺陷的部分抑制。cyc1-512 的四个回复突变体包含与 CYC1 基因座紧密连锁的染色体重排,断点;其中包括一个复制,一个可能的倒位,和两个相互易位。详细的遗传作图表明,两个相互易位之一发生在染色体 X 和 XII 的右臂之间,断点位于 CYC1 基因座的 3'端。这些结果表明,cyc1-512 中转录终止的缺陷可以通过多种方式恢复,包括将不同的染色体区域易位到 CYC1 基因座的 3'端、假定在或接近原始缺陷的局部变化,以及在与 CYC1 不同的另一位点发生突变。