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乳酸克鲁维酵母中编码Ap4A磷酸化酶II和线粒体bc1复合物14 kDa亚基VII的相关基因APA2和QCR7的分离与鉴定。

Isolation and characterisation of the linked genes APA2 and QCR7, coding for Ap4A phosphorylase II and the 14 kDa subunit VII of the mitochondrial bc1-complex in the yeast Kluyveromyces lactis.

作者信息

Mulder W, Scholten I H, van Roon H, Grivell L A

机构信息

Section for Molecular Biology, Biocentrum Amsterdam, The Netherlands.

出版信息

Biochim Biophys Acta. 1994 Nov 22;1219(3):719-23. doi: 10.1016/0167-4781(94)90235-6.

Abstract

We report the isolation and characterization of the KlQCR7 gene encoding subunit VII of the mitochondrial bc1 complex of the yeast Kluyveromyces lactis. The coding region is 69.3% identical to its counterpart in Saccharomyces cerevisiae (ScQCR7). Like the KlQCR8 gene (Mulder et al., accompanying paper) expression of the KlQCR7 gene during growth on glucose is high and can be further induced when cells are grown on non-fermentable carbon sources. The chromosomal linkage of the APA2 and QCR7 genes is conserved between S. cerevisiae and K. lactis. The intergenic regions containing the QCR7 promoters of the two yeasts, differ significantly in length and lack overall DNA sequence similarity, but they do share a binding site for the transcription factor complex HAP2/3/4. The KlQCR7 promoter contains, in addition, a CPF1 consensus binding site which is absent from ScQCR7. Deletion of a 35 bp region containing these two sites severely lowers the mRNA expression during growth on both glucose and ethanol/glycerol, but growth rate on both carbon sources is only mildly affected. Interestingly, in respect to the KlQCR7 gene, KlCPF1 seems to act as an important transcriptional activator, thus contrasting the proposed repressor function of ScCPF1 for the ScQCR8 gene of S. cerevisiae.

摘要

我们报道了乳酸克鲁维酵母线粒体bc1复合物编码亚基VII的KlQCR7基因的分离和特性。其编码区与酿酒酵母中的对应基因(ScQCR7)有69.3%的同源性。与KlQCR8基因(Mulder等人,同期论文)一样,KlQCR7基因在葡萄糖培养基上生长时表达量很高,当细胞在非发酵碳源上生长时表达量可进一步诱导。酿酒酵母和乳酸克鲁维酵母中APA2和QCR7基因的染色体连锁是保守的。两种酵母中包含QCR7启动子的基因间区域,在长度上有显著差异且缺乏整体DNA序列相似性,但它们确实共享转录因子复合物HAP2/3/4的结合位点。此外,KlQCR7启动子含有一个ScQCR7所没有的CPF1共有结合位点。缺失包含这两个位点的35 bp区域会严重降低在葡萄糖和乙醇/甘油培养基上生长时的mRNA表达,但在这两种碳源上的生长速率仅受到轻微影响。有趣的是,对于KlQCR7基因,KlCPF1似乎起着重要的转录激活作用,这与酿酒酵母中ScCPF1对ScQCR8基因所提出的抑制功能形成对比。

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