油酸诱导酵母基因SPS19编码过氧化物酶体β-氧化辅酶2,4-二烯酰辅酶a还原酶的adr1p依赖性调控

Aner Gurvitz , Leila Wabnegger , Hanspeter Rottensteiner , Ian W Dawes , Andreas Hartig , Helmut Ruis , Barbara Hamilton
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引用次数: 25

摘要

研究了酿酒酵母Adr1p对编码过氧化物酶体β-氧化辅酶2,4-二烯酰辅酶a还原酶的SPS19基因的转录调控作用。SPS19启动子包含一个结合Pip2p-Oaf1p转录因子的油酸反应元件和一个典型的adr1p结合元件,称为UAS1SPS19。Northern分析表明,在缺乏Adr1p的细胞中,SPS19的转录上调被取消。在adr1Δ突变体中,SPS19-lacZ报告基因的表达是静止的,而在含有多个ADR1拷贝的细胞中,SPS19-lacZ报告基因的表达异常升高。UAS1SPS19能够在重组Adr1p-LacZ和代表过氧化氢酶a基因启动子中相应adr1p结合元件的UAS1CTA1之间竞争形成特异性复合物,并直接与该融合蛋白相互作用。我们得出结论,在有脂肪酸存在的培养基中,SPS19的转录受到Pip2p-Oaf1p和Adr1p的直接调控。
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Adr1p-Dependent Regulation of the Oleic Acid-Inducible Yeast Gene SPS19 Encoding the Peroxisomal β-Oxidation Auxiliary Enzyme 2,4-Dienoyl-CoA Reductase

The role of Saccharomyces cerevisiae Adr1p was examined with respect to the transcriptional regulation of the SPS19 gene encoding the peroxisomal β-oxidation auxiliary enzyme 2,4-dienoyl-CoA reductase. The SPS19 promoter contains both an oleate response element that binds the Pip2p-Oaf1p transcription factor as well as a canonical Adr1p-binding element, termed UAS1SPS19. Northern analysis demonstrated that transcriptional up-regulation of SPS19 was abolished in cells devoid of Adr1p. Expression of an SPS19-lacZ reporter gene was shown to be quiescent in the adr1Δ mutant and abnormally elevated in cells containing multiple ADR1 copies. UAS1SPS19 was able to compete for formation of a specific complex between recombinant Adr1p-LacZ and UAS1CTA1 representing the corresponding Adr1p-binding element in the promoter of the catalase A gene, and to interact directly with this fusion protein. We conclude that in the presence of fatty acids in the medium transcription of SPS19 is directly regulated by both Pip2p-Oaf1p and Adr1p.

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