首页> 外文期刊>Nucleic acids research >Analysis of FAS3/ACC regulatory region of Saccharomyces cerevisiae: identification of a functional UASINO and sequences responsible for fatty acid mediated repression
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Analysis of FAS3/ACC regulatory region of Saccharomyces cerevisiae: identification of a functional UASINO and sequences responsible for fatty acid mediated repression

机译:酿酒酵母FAS3 / ACC调控区的分析:功能性UASINO和负责脂肪酸介导的阻遏序列的鉴定。

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We have determined the sequence of the FAS3/ACC regulatory region and mapped the transcription Initiation site. In this sequence, there are two putative UASINOsequences. Deletion and mutational analyses revealed that the UASINO sequence at nucleotldes ?719 to ?710 is functional. The expression of FAS3-lacZ reporter genes and the measurement of mRNA levels in regulatory mutants of phospholipid biosynthesis clearly indicated that FAS3 is regulated by inositol and chollne. Previous studies have shown that the genes coding for fatty acid synthase, FAS1 and FAS2, are regulated by inositol (Chirala, S.S. [1992] Proc. Natl. Acad. Scl. USA 89,10232–10236). Thus all three genes involved In saturated fatty acid biosynthesis are coordlnately regulated with phospholipid biosynthesis. Comparison of the UASINDsequences present in FAS1, FAS2, and FAS3 suggested that the functional sequence of this UAS element Is YTTCACATG. However, even when the functional UASIND was mutated, substantial expression of the FAS3-lacZ reporter gene was observed. Deletion analysis, electrophoretlc mobility shift assays, and expression using a heterologous reporter gene showed that the region between nucleotides ?840 and ?736 has two UAS elements. The same sequence seems to be responsible for fatty acld-medlated repression of FAS3. The presence of these additional UAS sequences explains why yeast does not require fatty acids even when repressing amounts of inositol and choline are present In the medium.
机译:我们已经确定了FAS3 / ACC调控区的序列,并绘制了转录起始位点。在此序列中,有两个假定的UAS INO 序列。缺失和突变分析表明,位于核苷酸719〜710的UAS INO 序列是有功能的。磷脂生物合成调控突变体中FAS3-lacZ报告基因的表达和mRNA水平的测量清楚地表明,FAS3受肌醇和胆碱调节。先前的研究表明,编码脂肪酸合酶FAS1和FAS2的基因受肌醇的调节(Chirala,S.S。[1992] Proc。Natl。Acad。Scl。USA 89,10232-10236)。因此,参与饱和脂肪酸生物合成的所有三个基因均由磷脂生物合成协调地调节。比较FAS1,FAS2和FAS3中存在的UAS IND 序列,表明该UAS元件的功能序列为YTTCACATG。但是,即使功能性UAS IND 发生了突变,也观察到了FAS3-lacZ报告基因的大量表达。缺失分析,电泳迁移率变动分析和使用异源报道基因的表达表明,核苷酸α840和β736之间的区域具有两个UAS元件。相同的序列似乎是导致脂肪性acld介导的FAS3抑制的原因。这些额外的UAS序列的存在解释了为什么即使培养基中存在抑制量的肌醇和胆碱,酵母也不需要脂肪酸。

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