PRS1 is a key member of the gene family encoding phosphoribosylpyrophosphate synthetase in Saccharomyces cerevisiae

被引:31
作者
Carter, AT
Beiche, F
HoveJensen, B
Narbad, A
Barker, PJ
Schweizer, LM
Schweizer, M
机构
[1] INST FOOD RES, DEPT GENET & MICROBIOL, NORWICH NR4 7UA, NORFOLK, ENGLAND
[2] UNIV COPENHAGEN, INST MOL BIOL, DEPT BIOL CHEM, DK-1307 COPENHAGEN K, DENMARK
[3] BABRAHAM INST, MICROCHEM FACIL, CAMBRIDGE CB2 4AT, ENGLAND
来源
MOLECULAR AND GENERAL GENETICS | 1997年 / 254卷 / 02期
基金
英国生物技术与生命科学研究理事会;
关键词
phosphoribosylpyrophosphate synthetase; gene family; nucleotide metabolism; Saccharomyces cerevisiae;
D O I
10.1007/s004380050402
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In Saccharomyces cerevisiae the metabolite phosphoribosyl-pyrophosphate (PRPP) is required for purine, pyrimidine, tryptophan and histidine biosynthesis. Enzymes that can synthesize PRPP can be encoded by at least four genes. We have studied 5-phospho-ribosyl-1(alpha)-pyrophosphate synthetases (PRS) genetically and biochemically. Each of the four genes, all of which are transcribed, has been disrupted in haploid yeast strains of each mating type and although all disruptants are able to grow on complete medium, differences in growth rate and enzyme activity suggest that disruption of PRS1 or PRS3 has a significant effect on cell metabolism, whereas disruption of PRS2 or PRS4 has little measurable effect. Using Western blot analysis with antisera raised against peptides derived from the non-homology region (NHR) and the N-terminal half of the PAS1 gene product it has been shown that the NHR is not removed by protein splicing. However, the fact that disruption of this gene causes the most dramatic decrease in cell growth rate and enzyme activity suggests that Prs1p may have a key structural or regulatory role in the production of PRPP in the cell.
引用
收藏
页码:148 / 156
页数:9
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