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首页> 外文期刊>FEBS letters. >The RNA polymerase I subunit Rpa12p interacts with the stress-responsive transcription factor Msn4p to regulate lipid metabolism in budding yeast
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The RNA polymerase I subunit Rpa12p interacts with the stress-responsive transcription factor Msn4p to regulate lipid metabolism in budding yeast

机译:RNA聚合酶I亚单位RPA12P与应力响应转录因子MSN4P相互作用以调节芽胺酵母中的脂质代谢

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摘要

In Saccharomyces cerevisiae, RPA12 encodes the small subunit of RNA polymerase I. Here, we demonstrate that Rpa12p interacts with the transcription factor Msn4p and prevents its binding to the promoter of AYR1 encoding Ayr1p (1-acyldihydroxyacetone phosphate reductase), a key enzyme involved in triacylglycerol biosynthesis and mobilization of nonpolar lipids. Deletion of RPA12 leads to triacylglycerol accumulation due to the binding of Msn4p to the promoter of AYR1 and activation of its transcription. The double deletion rpa12 Delta::ayr1 Delta caused a reduction in triacylglycerol levels. Our findings reveal that Rpa12p functions as a negative regulator of lipid metabolism by modulating nonpolar lipid biosynthesis through its interaction with Msn4p.
机译:在酿酒酵母中,RPA12编码RNA聚合酶的小亚基I.这里,在此证明RPA12P与转录因子MSN4P相互作用并防止其与编码AYR1P(1- acyLDROXY丙酮磷酸酯还原酶)的AYR1的启动子结合 三酰基甘油生物合成和动员非极性脂质。 由于MSN4P与Ayr1启动子的结合和其转录,导致RPA12的缺失导致三酰基甘油积累。 双删除RPA12δ::AYR1δ导致三酰基甘油水平降低。 我们的研究结果表明,通过与MSN4P的相互作用调节非极性脂质生物合成,RPA12P作为脂质代谢的负调节剂。

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