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酿酒酵母中MEL1转录本基础水平和诱导水平的调控

Regulation of basal and induced levels of the MEL1 transcript in Saccharomyces cerevisiae.

作者信息

Post-Beittenmiller M A, Hamilton R W, Hopper J E

出版信息

Mol Cell Biol. 1984 Jul;4(7):1238-45. doi: 10.1128/mcb.4.7.1238-1245.1984.

Abstract

The MEL1 gene in Saccharomyces cerevisiae is required for the production of alpha-galactosidase and for the catabolism of melibiose. Production of alpha-galactosidase is induced by galactose or melibiose and repressed by glucose. Inducibility is controlled by the positive and negative regulatory proteins GAL4 and GAL80, respectively. We have cloned the MEL1 gene to study its transcriptional expression and regulation. Evidence is presented that the MEL1 gene encodes alpha-galactosidase and that mel0 is a naturally occurring allele which lacks the alpha-galactosidase-coding sequences. RNAs prepared from wild-type cells and from cells carrying either the noninducible gal4-2 or GAL80S-100 allele grown on three different carbon sources were examined by Northern hybridization analyses. In wild-type cells under noninducing conditions, such as growth on glycerol-lactic acid, the MEL1 transcript was detected at a basal level which was 1 to 2% of the fully induced level. The basal level of expression was diminished in cells carrying the gal4-2 mutant allele but not in cells carrying the GAL80S-100 allele. The basal and induced RNA levels are repressed by glucose. Size determinations of the MEL1 transcripts detected in glycerol-lactic acid- and galactose-grown cells provided no evidence for two distinct transcripts.

摘要

酿酒酵母中的MEL1基因对于α-半乳糖苷酶的产生以及蜜二糖的分解代谢是必需的。α-半乳糖苷酶的产生由半乳糖或蜜二糖诱导,并被葡萄糖抑制。诱导性分别由正调控蛋白GAL4和负调控蛋白GAL80控制。我们克隆了MEL1基因以研究其转录表达和调控。有证据表明MEL1基因编码α-半乳糖苷酶,且mel0是一个天然存在的等位基因,它缺乏α-半乳糖苷酶编码序列。通过Northern杂交分析检测了从野生型细胞以及携带非诱导型gal4-2或GAL80S-100等位基因的细胞中提取的RNA,这些细胞在三种不同碳源上生长。在非诱导条件下,如在甘油 - 乳酸上生长的野生型细胞中,检测到MEL1转录本处于基础水平,该水平为完全诱导水平的1%至2%。携带gal4-2突变等位基因的细胞中表达的基础水平降低,但携带GAL80S-100等位基因的细胞中未降低。MEL1转录本的基础水平和诱导水平均被葡萄糖抑制。对在甘油 - 乳酸和半乳糖培养的细胞中检测到的MEL1转录本进行大小测定,未发现存在两种不同转录本的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b375/368904/f142fcf7b0f2/molcellb00149-0057-a.jpg

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