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一个多拷贝抑制基因MSS10,可在含有STA10阻遏基因的酿酒酵母菌株中恢复STA2的表达。

A multicopy suppressor gene, MSS10, restores STA2 expression in Saccharomyces cerevisiae strains containing the STA10 repressor gene.

作者信息

Lambrechts M G, Sollitti P, Marmur J, Pretorius I S

机构信息

Department of Microbiology and Institute for Wine Biotechnology, University of Stellenbosch, Stellenbosch 7600, South Africa.

出版信息

Curr Genet. 1996 May;29(6):523-9.

PMID:8662191
Abstract

Transcription of the three unlinked, homologous STA1-3 glucoamylase-encoding genes, involved in starch degradation by Saccharomyces cerevisiae, was previously shown to be down-regulated by the presence of STA10, acting via three upstream repression sequence regions that were identified in the STA2 promoter. Here we report the cloning and characterization of a putative transcriptional activator gene, MSS10 (multicopy suppressor of STA10), which, when present in multiple copies, overcomes STA10 repression. Deletion of MSS10, located on chromosome XV, resulted in media-specific extinction of glucoamylase synthesis. The nucleotide sequence of MSS10 is identical to three other genes from S. cerevisiae identified as: FUP1, a gene that enhances iron-limited growth; PHD2, a gene identified for its ability to induce pseudohyphal growth in diploid cells grown on nitrogen-limited media; and MSN1, a gene encoding a transcriptional activator involved in invertase regulation.

摘要

酿酒酵母中参与淀粉降解的三个不连锁的同源STA1 - 3葡糖淀粉酶编码基因的转录,先前已表明会受到STA10的抑制,STA10通过在STA2启动子中鉴定出的三个上游阻遏序列区域发挥作用。在此,我们报告了一个假定的转录激活基因MSS10(STA10的多拷贝抑制子)的克隆和表征,当它以多拷贝存在时,可克服STA10的抑制作用。位于第十五号染色体上的MSS10缺失,导致葡糖淀粉酶合成在培养基特异性条件下消失。MSS10的核苷酸序列与酿酒酵母的其他三个基因相同,这三个基因分别为:FUP1,一个增强铁限制生长的基因;PHD2,一个因其在氮限制培养基上生长的二倍体细胞中诱导假菌丝生长的能力而被鉴定的基因;以及MSN1,一个编码参与转化酶调节的转录激活因子的基因。

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