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酿酒酵母尿苷单磷酸激酶编码基因的遗传特性鉴定与分离

Genetic characterization and isolation of the Saccharomyces cerevisiae gene coding for uridine monophosphokinase.

作者信息

Liljelund P, Lacroute F

出版信息

Mol Gen Genet. 1986 Oct;205(1):74-81. doi: 10.1007/BF02428034.

Abstract

We selected a 5-fluorouracil-resistant, thermosensitive mutant of the uridine monophosphokinase step in Saccharomyces cerevisiae. The mutant displays very weak thermolabile uridine monophosphokinase activity and wild-type uridine diphosphokinase activity. Growth of the mutant at the non-permissive temperature causes immediate reduction of pyrimidine triphosphate pools to 10% of the wild-type level as well as significantly lowering total RNA and protein synthesis. These conditions also provoke derepression of the first gene of the pathway, URA2, at both the levels of enzymatic activity and transcription. The mutation segregates independently of all known genes of the pyrimidine biosynthetic pathway. The corresponding gene has been isolated on a 4.8 kb fragment by complementation of the mutant phenotype. The new gene, named URA6, codes for a 2.2 kb polyadenylated messenger RNA, exists in a single copy per haploid genome, and was mapped to the centromere of chromosome XI.

摘要

我们选择了酿酒酵母中尿苷单磷酸激酶步骤的一个对5-氟尿嘧啶耐药的热敏突变体。该突变体表现出非常弱的热不稳定尿苷单磷酸激酶活性和野生型尿苷二磷酸激酶活性。突变体在非允许温度下生长会导致嘧啶三磷酸池立即减少至野生型水平的10%,同时显著降低总RNA和蛋白质合成。这些条件还会在酶活性和转录水平上引发该途径第一个基因URA2的去阻遏。该突变与嘧啶生物合成途径的所有已知基因独立分离。通过突变体表型的互补,在一个4.8 kb的片段上分离出了相应的基因。这个新基因名为URA6,编码一个2.2 kb的多聚腺苷酸化信使RNA,每个单倍体基因组中存在一个拷贝,并被定位到染色体XI的着丝粒上。

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