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酿酒酵母URA5基因的结构与表达

Structure and expression of the URA5 gene of Saccharomyces cerevisiae.

作者信息

de Montigny J, Belarbi A, Hubert J C, Lacroute F

机构信息

Laboratoire de Génétique Physiologique, I.B.M.C. du C.N.R.S., Strasbourg, France.

出版信息

Mol Gen Genet. 1989 Feb;215(3):455-62. doi: 10.1007/BF00427043.

DOI:10.1007/BF00427043
PMID:2651891
Abstract

The URA5 gene of Saccharomyces cerevisiae encodes orotate phosphoribosyl transferase (EC 2.4.2.10; OPRTase) which catalyses the transformation of orotate to OMP in the pyrimidine pathway. We present in this paper the cloning and the sequencing of this gene, the last in the yeast pyrimidine pathway to be cloned. We have deduced the protein sequence of the OPRTase of S. cerevisiae from the DNA sequence and compared it to that of Escherichia coli, Podospora anserina and Dictyostelium discoideum. Some important similarities in the structure of these four proteins have been found. Finally, we have quantified the transcription of the URA5 gene in different physiological conditions and confirmed that it was not under the control of UTP or any intermediary product of the pathway.

摘要

酿酒酵母的URA5基因编码乳清酸磷酸核糖转移酶(EC 2.4.2.10;OPRTase),该酶在嘧啶途径中催化乳清酸转化为OMP。我们在本文中展示了该基因的克隆和测序,这是酵母嘧啶途径中最后一个被克隆的基因。我们从DNA序列推导了酿酒酵母OPRTase的蛋白质序列,并将其与大肠杆菌、嗜鸟粪盘菌和盘基网柄菌的序列进行了比较。发现这四种蛋白质在结构上有一些重要的相似之处。最后,我们定量了URA5基因在不同生理条件下的转录,并证实其不受UTP或该途径任何中间产物的调控。

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1
Structure and expression of the URA5 gene of Saccharomyces cerevisiae.酿酒酵母URA5基因的结构与表达
Mol Gen Genet. 1989 Feb;215(3):455-62. doi: 10.1007/BF00427043.
2
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本文引用的文献

1
Measure of asymmetrical transcription of the yeast OMP decarboxylase gene expressed in yeast or in E. coli.酵母或大肠杆菌中表达的酵母 OMP 脱羧酶基因不对称转录的测量。
Curr Genet. 1980 Oct;2(2):103-7. doi: 10.1007/BF00420621.
2
Constitutive mutants for orotidine 5 phosphate decarboxylase and dihydroorotic acid dehydrogenase in Saccharomyces cerevisiae.酿酒酵母中乳清酸核苷-5′-磷酸脱羧酶和二氢乳清酸脱氢酶的组成型突变体。
Curr Genet. 1980 Jul;2(1):39-44. doi: 10.1007/BF00445692.
3
Effect of ochre nonsense mutations on yeast URA1 mRNA stability.
解析酵母中嘧啶从头生物合成途径上的选择压力。
BMC Evol Biol. 2015 Oct 28;15:232. doi: 10.1186/s12862-015-0515-x.
4
Regulation of amino acid, nucleotide, and phosphate metabolism in Saccharomyces cerevisiae.酿酒酵母中氨基酸、核苷酸和磷酸盐代谢的调节。
Genetics. 2012 Mar;190(3):885-929. doi: 10.1534/genetics.111.133306.
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Use of a ura5+-lys7+ cassette to construct unmarked gene knock-ins in Schizosaccharomyces pombe.利用 ura5+-lys7+ 盒构建酿酒酵母无标记基因敲入。
Curr Genet. 2012 Feb;58(1):59-64. doi: 10.1007/s00294-011-0360-4. Epub 2011 Dec 25.
6
Horizontal and vertical growth of S. cerevisiae metabolic network.酿酒酵母代谢网络的水平和垂直生长。
BMC Evol Biol. 2011 Oct 14;11:301. doi: 10.1186/1471-2148-11-301.
7
Ectopic expression of URA3 can influence the virulence phenotypes and proteome of Candida albicans but can be overcome by targeted reintegration of URA3 at the RPS10 locus.URA3的异位表达可影响白色念珠菌的毒力表型和蛋白质组,但可通过将URA3靶向重新整合到RPS10位点来克服。
Eukaryot Cell. 2004 Aug;3(4):900-9. doi: 10.1128/EC.3.4.900-909.2004.
8
Rare homologous gene targeting in Histoplasma capsulatum: disruption of the URA5Hc gene by allelic replacement.荚膜组织胞浆菌中罕见的同源基因靶向:通过等位基因置换破坏URA5Hc基因
J Bacteriol. 1998 Oct;180(19):5135-43. doi: 10.1128/JB.180.19.5135-5143.1998.
9
Heterospecific cloning of Arabidopsis thaliana cDNAs by direct complementation of pyrimidine auxotrophic mutants of Saccharomyces cerevisiae. I. Cloning and sequence analysis of two cDNAs catalysing the second, fifth and sixth steps of the de novo pyrimidine biosynthesis pathway.通过酿酒酵母嘧啶营养缺陷型突变体的直接互补对拟南芥cDNA进行异源特异性克隆。I. 催化从头嘧啶生物合成途径第二步、第五步和第六步反应的两个cDNA的克隆与序列分析
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Gene. 1980 Oct;11(1-2):11-9. doi: 10.1016/0378-1119(80)90082-7.