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聚球藻属蓝细菌PCC 7002中脂肪酸去饱和酶基因的温度调节型mRNA积累与稳定

Temperature-regulated mRNA accumulation and stabilization for fatty acid desaturase genes in the cyanobacterium Synechococcus sp. strain PCC 7002.

作者信息

Sakamoto T, Bryant D A

机构信息

Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park 16802, USA.

出版信息

Mol Microbiol. 1997 Mar;23(6):1281-92. doi: 10.1046/j.1365-2958.1997.3071676.x.

Abstract

Cyanobacteria acclimate to low-temperature conditions by desaturating their membrane lipids. The desB (omega 3 desaturase) and desC (delta 9 desaturase) genes of Synechococcus sp. strain PCC 7002 were cloned and characterized, and the expression of the desA (delta 12 desaturase), desB and desC genes was studied as a function of temperature. The steady-state mRNA abundance for the desA gene was threefold higher in cells grown at 22 degrees C than in cells grown at 38 degrees C. desB transcripts were not detected at 38 degrees C, but were abundant in cells grown at 22 degrees C. Levels of desC mRNA were similar at both growth temperatures. The mRNA levels of each desaturase gene increased within 15 min of a temperature shift-down to 22 degrees C, and mRNA levels recovered within 15 min after a shift-up to 38 degrees C. The cold-induced accumulation of transcripts from the desA and desB genes was suppressed by the addition of chloramphenicol, but the transient elevation of the desC transcript levels at 22 degrees C was not affected by chloramphenicol. The half-lives of the desA and desB mRNAs were significantly longer in cells grown at 22 degrees C than in cells grown at 38 degrees C, but the desC mRNA had a similar half-life at both temperatures. These studies reveal three patterns of temperature regulation for the desaturase genes, whose expression is tightly controlled by a combination of mRNA synthesis and stabilization. These studies demonstrate that elevation of desaturase mRNA levels is not the rate-limiting event during the low-temperature acclimation of cyanobacteria.

摘要

蓝细菌通过使膜脂去饱和来适应低温条件。克隆并表征了聚球藻属菌株PCC 7002的desB(ω-3去饱和酶)和desC(δ-9去饱和酶)基因,并研究了desA(δ-12去饱和酶)、desB和desC基因的表达随温度的变化。desA基因的稳态mRNA丰度在22℃生长的细胞中比在38℃生长的细胞中高3倍。在38℃未检测到desB转录本,但在22℃生长的细胞中大量存在。desC mRNA水平在两个生长温度下相似。每种去饱和酶基因的mRNA水平在温度下调至22℃后的15分钟内增加,在温度上调至38℃后的15分钟内恢复。desA和desB基因转录本的冷诱导积累被氯霉素抑制,但氯霉素不影响desC转录本水平在22℃时的短暂升高。desA和desB mRNA的半衰期在22℃生长的细胞中比在38℃生长的细胞中长得多,但desC mRNA在两个温度下具有相似的半衰期。这些研究揭示了去饱和酶基因的三种温度调节模式,其表达受mRNA合成和稳定性的组合严格控制。这些研究表明,去饱和酶mRNA水平的升高不是蓝细菌低温适应过程中的限速事件。

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