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基于对5-氟乳清酸的抗性,对缺乏尿苷一磷酸合酶活性的盘基网柄菌突变体进行正向选择。

Positive selection for Dictyostelium discoideum mutants lacking UMP synthase activity based on resistance to 5-fluoroorotic acid.

作者信息

Kalpaxis D, Zündorf I, Werner H, Reindl N, Boy-Marcotte E, Jacquet M, Dingermann T

机构信息

Institut für Biochemie der Medizinischen Fakultät, Universität Erlangen-Nürnberg, Federal Republic of Germany.

出版信息

Mol Gen Genet. 1991 Mar;225(3):492-500. doi: 10.1007/BF00261692.

Abstract

In the cellular slime mould Dictyostelium discoideum the two enzymatic activities of the pyrimidine pathway, orotidine-5'-phosphate decarboxylase (EC 4.1.1.23; OMPdecase) and orotate phosphoribosyl transferase (EC 2.4.2.10; OPRTase), are encoded by a single gene (DdPYR5-6). As in higher eukaryotes the bifunctional enzyme is referred to as UMP synthase. Here we present a method that allows efficient generation and selection of mutants lacking UMP synthase. D. discoideum cells are transformed with either of two different types of plasmids. One plasmid type contains no sequences homologous to the UMP synthase gene whereas the other type contains at least parts of this gene. UMP synthase- mutants, which were positively selected for in the presence of 5-fluoroorotic acid (5-FOA), were obtained with both plasmids. However, mutation rates were at least one order of magnitude higher if plasmids containing various portions of the UMP synthase gene were used as opposed to plasmids that lack any homology to the UMP synthase locus. Several mutant strains were extensively characterized. These strains lack OMPdecase activity and exhibit in addition to 5-FOA resistance a ura- phenotype. All mutants carry UMP synthase loci with deletions of various extents but integration of transforming plasmids was not detected. This efficient generation of 5-FOA resistance is part of a proposed complex selection scheme which allows multiple rounds of transformation of D. discoideum.

摘要

在细胞黏菌盘基网柄菌中,嘧啶途径的两种酶活性,即乳清苷-5'-磷酸脱羧酶(EC 4.1.1.23;OMP脱羧酶)和乳清酸磷酸核糖基转移酶(EC 2.4.2.10;OPRTase),由单个基因(DdPYR5-6)编码。与高等真核生物一样,这种双功能酶被称为UMP合酶。在此,我们提出一种方法,可有效生成和筛选缺乏UMP合酶的突变体。用两种不同类型的质粒之一转化盘基网柄菌细胞。一种质粒类型不包含与UMP合酶基因同源的序列,而另一种类型至少包含该基因的部分序列。在5-氟乳清酸(5-FOA)存在下进行正向选择获得了UMP合酶突变体,两种质粒均得到了该突变体。然而,如果使用含有UMP合酶基因不同部分的质粒,与缺乏与UMP合酶基因座任何同源性的质粒相比突变率至少高一个数量级。对几个突变菌株进行了广泛表征。这些菌株缺乏OMP脱羧酶活性,除了对5-FOA具有抗性外还表现出尿嘧啶缺陷型表型。所有突变体都携带不同程度缺失的UMP合酶基因座,但未检测到转化质粒的整合。这种有效产生5-FOA抗性是所提出的复杂选择方案的一部分,该方案允许对盘基网柄菌进行多轮转化。

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