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乳酸克鲁维酵母中编码法呢基二磷酸合酶和线粒体bc1复合物11 kDa VIII亚基的相关基因FPS1和QCR8的分离与鉴定。

Isolation and characterisation of the linked genes, FPS1 and QCR8, coding for farnesyl-diphosphate synthase and the 11 kDa subunit VIII of the mitochondrial bc1-complex in the yeast Kluyveromyces lactis.

作者信息

Mulder W, Scholten I H, Nagelkerken B, 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):713-8. doi: 10.1016/0167-4781(94)90234-8.

Abstract

The KlQCR8 gene of the yeast Kluyveromyces lactis encoding subunit VIII of the mitochondrial bc1 complex is 70.2% identical to its counterpart in Saccharomyces cerevisiae (ScQCR8). As in S. cerevisiae, chromosomal linkage between the K. lactis QCR8 and FPS1 genes is conserved, the two genes being separated by only 292 bp. Disruption of the KlQCR8 gene results in a respiratory-deficient phenotype. Compared with S. cerevisiae, expression of the KlQCR8 gene in glucose-grown cells is relatively high, yet is significantly induced when the cells are grown on non-fermentable carbon sources. The QCR8 promoters regions of the two yeasts lack overall DNA sequence similarity, but share DNA-binding sites for the transcription factors ABF1, CPF1 and HAP2/3/4. Deletion from the KlQCR8 promoter of a 93 bp region containing these sites significantly lowers mRNA levels during growth on either glucose or ethanol/glycerol, with a consequent reduction of growth rate on ethanol/glycerol.

摘要

乳酸克鲁维酵母的KlQCR8基因编码线粒体bc1复合物的亚基VIII,与酿酒酵母中的对应基因(ScQCR8)有70.2%的同一性。与酿酒酵母一样,乳酸克鲁维酵母的QCR8和FPS1基因之间的染色体连锁是保守的,这两个基因仅相隔292 bp。KlQCR8基因的破坏导致呼吸缺陷表型。与酿酒酵母相比,KlQCR8基因在以葡萄糖生长的细胞中的表达相对较高,但当细胞在非发酵碳源上生长时会显著诱导表达。两种酵母的QCR8启动子区域缺乏整体DNA序列相似性,但共享转录因子ABF1、CPF1和HAP2/3/4的DNA结合位点。从KlQCR8启动子中删除包含这些位点的93 bp区域,会显著降低在葡萄糖或乙醇/甘油上生长期间的mRNA水平,从而导致在乙醇/甘油上的生长速率降低。

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