Aon M A, Cortassa S
Instituto Tecnológico de Chascomús (INTECH, SECYT/CONICET), Casilla Correo 164, 7130 Chascomús, Buenos Aires, Argentina.
Curr Microbiol. 1999 Jan;38(1):57-60. doi: 10.1007/pl00006773.
We have studied the effect of disrupting catabolite (de)repression genes SNF1, SNF4, and MIG1 on the cell cycle behavior of the CEN. PK122 wild type (WT) strain of Saccharomyces cerevisiae by flow cytometry in glucose-limited chemostat cultures or batch growth in the presence of different carbon sources. Through a combination of flow cytometry of propidium iodide-stained cells and mathematical modeling we showed that the deletion of the SNF4 gene provoked a decrease in the length of G1 with respect to the WT strain along with a smaller difference in the cell cycle length of parent and daughter cells. snf1 and mig1 mutants exhibited slightly shorter G1 respect to the WT. Additionally, in the mig1 mutant the cell cycle length of parent and daughter cells was slightly altered. The results obtained are in agreement with the view that the SNF4 gene is involved in the regulation of cell cycle in yeast.
我们通过流式细胞术研究了破坏分解代谢(去)阻遏基因SNF1、SNF4和MIG1对酿酒酵母CEN.PK122野生型(WT)菌株在葡萄糖限制恒化器培养或不同碳源存在下分批生长时细胞周期行为的影响。通过碘化丙啶染色细胞的流式细胞术和数学建模相结合的方法,我们发现,与WT菌株相比,SNF4基因的缺失导致G1期长度缩短,同时母细胞和子细胞的细胞周期长度差异减小。snf1和mig1突变体相对于WT表现出略短的G1期。此外,在mig1突变体中,母细胞和子细胞的细胞周期长度略有改变。所得结果与SNF4基因参与酵母细胞周期调控的观点一致。