Swoboda R K, Bertram G, Delbrück S, Ernst J F, Gow N A, Gooday G W, Brown A J
University of Aberdeen, Marischal College, UK.
Mol Microbiol. 1994 Aug;13(4):663-72. doi: 10.1111/j.1365-2958.1994.tb00460.x.
The levels of pyruvate kinase (PYK1), alcohol dehydrogenase (ADH1), phosphoglycerate kinase (PGK1) and phosphoglycerate mutase (GPM1) mRNAs were measured during batch growth and during the yeast-to-hyphal transition in Candida albicans. The four mRNAs behaved in a similar fashion. PYK1, ADH1, PGK1 and GPM1 mRNA levels were shown to increase dramatically during the exponential growth phase of the yeast form, and then to decrease to relatively low levels in the stationary phase. The dimorphic transition was induced using two sets of conditions: (i) an increase in temperature (from 25 degrees C to 37 degrees C) combined with the addition of serum to the medium; and (ii) an increase in temperature (from 25 degrees C to 37 degrees C) and an increase in pH of the growth medium (from pH 4.5 to pH 6.5). Additional cultures were analysed to control for the addition of serum, and for changes in temperature or pH. Immediately following dilution of late-exponential cells into fresh media the levels of all four glycolytic mRNAs decreased rapidly in contrast to the ACT1 mRNA control, the level of which increased under most conditions. The recovery of glycolytic mRNA levels depended on the culture conditions, but there was no direct correlation with the formation of germ tubes, with the addition of serum to the medium, the increase in culture temperature, the medium pH, or the glucose concentration. This indicates that the changes in glycolytic gene expression that accompany the dimorphic transition in C. albicans reflect the underlying physiological status of the cells during morphogenesis and not alterations to cell shape.
在白色念珠菌的分批培养生长过程以及酵母形态向菌丝形态转变过程中,对丙酮酸激酶(PYK1)、乙醇脱氢酶(ADH1)、磷酸甘油酸激酶(PGK1)和磷酸甘油酸变位酶(GPM1)的mRNA水平进行了测定。这四种mRNA的表现方式相似。结果显示,PYK1、ADH1、PGK1和GPM1的mRNA水平在酵母形态的指数生长期显著增加,然后在稳定期降至相对较低水平。采用两组条件诱导双态转变:(i)温度升高(从25℃升至37℃)并向培养基中添加血清;(ii)温度升高(从25℃升至37℃)以及生长培养基的pH值升高(从pH 4.5升至pH 6.5)。对额外的培养物进行分析,以控制血清添加以及温度或pH值的变化。与ACT1 mRNA对照相反,在将指数生长期后期的细胞稀释到新鲜培养基后,所有四种糖酵解mRNA的水平迅速下降,而ACT1 mRNA在大多数条件下水平升高。糖酵解mRNA水平的恢复取决于培养条件,但与芽管的形成、向培养基中添加血清、培养温度升高、培养基pH值或葡萄糖浓度没有直接相关性。这表明白色念珠菌双态转变过程中伴随的糖酵解基因表达变化反映了细胞在形态发生过程中的潜在生理状态,而非细胞形状的改变。