Lydall D, Ammerer G, Nasmyth K
Research Institute of Molecular Pathology (IMP), University of Vienna, Austria.
Genes Dev. 1991 Dec;5(12B):2405-19. doi: 10.1101/gad.5.12b.2405.
In the yeast Saccharomyces cerevisiae cell cycle-regulated SW15 transcription is essential for ensuring that mother and not daughter cells switch mating type. We have identified a 55-bp promoter sequence that appears to be responsible for restricting transcription to the late S, G2, and M phases of the cell cycle. Two proteins, MCM1, a transcription factor described previously, and SFF (SWI five factor, a newly identified factor) bind this sequence in vitro. MCM1 binds the DNA tightly on its own, but SFF will only bind as part of a ternary complex with MCM1. We observe a strong correlation between the ability of mutated SWI5 promoter sequences to form a ternary MCM1-SFF-containing complex in vitro and to activate transcription in vivo, which suggests that efficient transcription requires that both proteins bind DNA. Through its interactions with cell type-specific coactivators and corepressors, MCM1 controls cell type-specific expression of pheromone and receptor genes. By analogy, we propose that SFF enables MCM1 to function as a part of a cell cycle-regulated transcription complex.
在酿酒酵母中,细胞周期调控的SWI5转录对于确保母细胞而非子细胞转换交配型至关重要。我们鉴定出一段55个碱基对的启动子序列,它似乎负责将转录限制在细胞周期的S期晚期、G2期和M期。两种蛋白质,即先前描述的转录因子MCM1和新鉴定的因子SFF(SWI5因子),在体外结合该序列。MCM1自身就能紧密结合DNA,但SFF仅作为与MCM1的三元复合物的一部分才能结合。我们观察到,体外突变的SWI5启动子序列形成含MCM1 - SFF三元复合物的能力与体内激活转录的能力之间存在很强的相关性,这表明高效转录需要这两种蛋白质都结合DNA。通过与细胞类型特异性共激活因子和共抑制因子的相互作用,MCM1控制信息素和受体基因的细胞类型特异性表达。类似地,我们提出SFF使MCM1能够作为细胞周期调控转录复合物的一部分发挥作用。