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具有去阻遏硫胺素基因表达的酿酒酵母突变体的分离与鉴定。

Isolation and characterization of Saccharomyces cerevisiae mutants with derepressed thiamine gene expression.

作者信息

Burrows R J, Byrne K L, Meacock P A

机构信息

Department of Genetics, University of Leicester, University Road, Leicester LE1 7RH, UK.

出版信息

Yeast. 2000 Dec;16(16):1497-508. doi: 10.1002/1097-0061(200012)16:16<1497::AID-YEA645>3.0.CO;2-Z.

Abstract

Using a THI4-lacZ reporter gene, mutant strains have been isolated that display constitutive expression of thiamine genes in the presence of normally repressing levels of exogenous thiamine. In total, eight strains were isolated in which this derepressed expression on thiamine (Det(-)) phenotype was the result of single gene mutations. The Det(-) mutations of three of these strains were partially dominant in a heterozygous diploid configuration, whereas the other five were recessive. The partially dominant mutants DET1, DET12 and DET13, and the recessive mutant det2, all showed derepressed THI4-lacZ expression levels comparable to those of a fully induced normal strain. Use of other promoter-lacZ gene fusions revealed that these four mutants were pleiotropic; expression levels of all thiamine-regulated genes tested were also derepressed. Genetic analysis of the four mutants suggested that det2 and DET13 were allelic, whereas the others were at different loci; these four mutations therefore represent three different genes. None of the mutations were allelic with THI80, mutations of which have previously been shown to confer derepression on thiamine-regulated genes. Also, intracellular thiamine levels were close to normal and none of the four mutants excreted thiamine into the growth medium. All mutant strains were found to be prototrophic for thiamine and none of those tested were compromised for thiamine uptake. It is possible that some may be alleles of, or interact with, the activator gene THI3. Taken together, these results imply that DET1, det2, DET12 and DET13 represent new genes encoding negative regulators of thiamine-repressed genes.

摘要

利用THI4 - lacZ报告基因,已分离出突变菌株,这些菌株在外源硫胺素处于正常抑制水平时仍表现出硫胺素基因的组成型表达。总共分离出了八个菌株,其中这种硫胺素去抑制表达(Det(-))表型是单基因突变的结果。其中三个菌株的Det(-)突变在杂合二倍体构型中部分显性,而另外五个是隐性的。部分显性突变体DET1、DET12和DET13,以及隐性突变体det2,其THI4 - lacZ表达水平的去抑制程度均与完全诱导的正常菌株相当。使用其他启动子 - lacZ基因融合表明,这四个突变体具有多效性;所有测试的硫胺素调节基因的表达水平也都去抑制。对这四个突变体的遗传分析表明,det2和DET13是等位基因,而其他的位于不同位点;因此这四个突变代表三个不同的基因。这些突变均与THI80无等位关系,此前已证明THI80突变可导致硫胺素调节基因的去抑制。此外,细胞内硫胺素水平接近正常,且这四个突变体均未向生长培养基中分泌硫胺素。所有突变菌株对硫胺素都是原养型的,且所测试的菌株中没有一个在硫胺素摄取方面受损。有可能其中一些可能是激活基因THI3的等位基因,或与THI3相互作用。综上所述,这些结果表明DET1、det2、DET12和DET13代表编码硫胺素抑制基因负调控因子的新基因。

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