Fluctuations in glycolytic mRNA levels during morphogenesis in Candida albicans reflect underlying changes in growth and are not a response to cellular dimorphism

生物 磷酸甘油酸激酶 糖酵解 白色念珠菌 丙酮酸激酶 酵母 信使核糖核酸 生物化学 基因表达 磷酸甘油酸变位酶 分子生物学 基因 微生物学
作者
Rolf Swoboda,Gwyneth Bertram,Sebastian Delbrück,J F Ernst,Neil A. R. Gow,G. W. Gooday,A. J. P. Brown
出处
期刊:Molecular Microbiology [Wiley]
卷期号:13 (4): 663-672 被引量:63
标识
DOI:10.1111/j.1365-2958.1994.tb00460.x
摘要

Summary The levels of pyruvate kinase ( PYK ), alcohol dehydrogenase ( ADH 1), phosphoglycerate kinase ( PGK 1) and phosphoglycerate mutase ( GPM 1) mRNAs were measured during batch growth and during the yeast‐to‐hyphal transition in Candida albicans. The four mRNAs behaved in a similar fashion. PYK 1, ADH 1, PGK 1 and GPM 1 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°C to 37°C) combined with the addition of serum to the medium; and (ii) an increase in temperature (from 25°C to 37°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 ACT 1 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.
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