Characterization of the phosphoribosylpyrophosphate synthetase gene from Candida albicans.

T. Payne, R. Calderone
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引用次数: 3

Abstract

Phosphoribosylpyrophosphate (PRPP) synthetase catalyzes the transfer of phosphate from ATP to D-ribose-5-phosphate during the synthesis of purine and pyrimidine nucleotides and tryptophan and histidine biosynthesis in a variety of organisms. We cloned and sequenced the PRPP synthetase gene (PRS1) of Candida albicans because, in Saccharomyces cerevisiae, a deficiency in PRPP synthetase activity interacts with a mutation in ELM4-1 (elongated morphology) to cause constitutive pseudohyphal growth in nitrogen-rich media. In order to study the role of the C. albicans PRS1 in growth and morphogenesis, we used gene disruption to isolate PRS1 mutants; however, while heterozygous PRS1 clones were readily obtained, homozygous, null strains were not recovered indicating that PRS1 is probably essential for growth of the organism. Heterozygotes in PRS1 produced approximately 35% less PRPP synthetase (P = 0.0004) and exhibited a similar reduction in transcript levels. Confirmation of a heterozygous, single disruption in PRS1 was obtained by I-SceI digestion of chromosomal-sized DNA and Southern blot hybridizations. While no role in morphogenesis is elucidated by this work, the data strongly suggests that PRS1 is an essential gene in C. albicans and supports earlier results that indicated the presence of a single PRS gene in C. albicans.
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白色念珠菌磷酸核糖焦磷酸合成酶基因的研究。
磷酸核糖基焦磷酸合成酶(PRPP)在多种生物合成嘌呤和嘧啶核苷酸以及色氨酸和组氨酸的过程中催化磷酸从ATP向d -核糖-5-磷酸的转移。我们克隆并测序了白色念珠菌的PRPP合成酶基因(PRS1),因为在酿酒酵母中,PRPP合成酶活性的缺乏与ELM4-1(细长形态)突变相互作用,导致富氮培养基中组成性假菌丝生长。为了研究白色念珠菌PRS1在生长和形态发生中的作用,我们采用基因破坏分离PRS1突变体;然而,虽然很容易获得杂合的PRS1克隆,但没有恢复纯合的零菌株,这表明PRS1可能是生物体生长所必需的。PRS1中的杂合子产生的PRPP合成酶减少了约35% (P = 0.0004),并且转录水平也出现了类似的降低。通过I-SceI消化染色体大小的DNA和Southern杂交,证实了PRS1的杂合,单断裂。虽然这项工作没有阐明PRS1在形态发生中的作用,但数据强烈表明PRS1是白色念珠菌的必需基因,并支持先前的结果,即白色念珠菌中存在单个PRS基因。
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