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两种酵母酰基辅酶A:固醇酰基转移酶的血红素调节表达参与固醇酯化对无氧状态的特异性反应。

Heme-regulated expression of two yeast acyl-CoA:sterol acyltransferases is involved in the specific response of sterol esterification to anaerobiosis.

作者信息

Valachovic Martin, Klobucníková Vlasta, Griac Peter, Hapala Ivan

机构信息

Institute of Animal Biochemistry and Genetics, Slovak Academy of Sciences, 900 28, Ivanka pri Dunaji, Slovak Republic.

出版信息

FEMS Microbiol Lett. 2002 Jan 2;206(1):121-5. doi: 10.1111/j.1574-6968.2002.tb10996.x.

Abstract

Sterol esterification in Saccharomyces cerevisiae is catalyzed by two acyl-CoA:sterol acyltransferases encoded by the genes ARE1 and ARE2. Using double mutants in the HEM1 gene and individual ARE genes we demonstrated that the relative contribution of these two enzymes to sterol esterification was dependent on cellular heme status. Observed changes in sterol esterification could be explained by a different effect of heme on the transcription of both genes: while the ARE1 transcript level was elevated in heme-deficient and anaerobic cells, the ARE2 gene transcript was more abundant in aerobic cells competent for heme synthesis. Our results indicate that transcriptional regulation of ARE genes by heme and specific substrate preferences of Are1p and Are2p may be involved in the adaptation of yeast sterol metabolism to hypoxia.

摘要

酿酒酵母中的甾醇酯化由ARE1和ARE2基因编码的两种酰基辅酶A:甾醇酰基转移酶催化。利用HEM1基因和单个ARE基因的双突变体,我们证明这两种酶对甾醇酯化的相对贡献取决于细胞的血红素状态。观察到的甾醇酯化变化可以通过血红素对这两个基因转录的不同影响来解释:虽然ARE1转录水平在血红素缺乏和厌氧细胞中升高,但ARE2基因转录本在能够合成血红素的需氧细胞中更为丰富。我们的结果表明,血红素对ARE基因的转录调控以及Are1p和Are2p的特定底物偏好可能参与了酵母甾醇代谢对缺氧的适应。

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