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首页> 外文期刊>Molecular and Cellular Biology >Expression of the Saccharomyces cerevisiae inositol-1-phosphate synthase (INO1) gene is regulated by factors that affect phospholipid synthesis.
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Expression of the Saccharomyces cerevisiae inositol-1-phosphate synthase (INO1) gene is regulated by factors that affect phospholipid synthesis.

机译:酿酒酵母肌醇-1-磷酸合酶(INO1)基因的表达受影响磷脂合成的因素调控。

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The INO1 gene of Saccharomyces cerevisiae encodes the regulated enzyme inositol-1-phosphate synthase, which catalyzes the first committed step in the synthesis of inositol-containing phospholipids. The expression of this gene was analyzed under conditions known to regulate phospholipid synthesis. RNA blot hybridization with a genomic clone for INO1 detected two RNA species of 1.8 and 0.6 kb. The abundance of the 1.8-kb RNA was greatly decreased when the cells were grown in the presence of the phospholipid precursor inositol, as was the enzyme activity of the synthase. Complementation analysis showed that this transcript encoded the INO1 gene product. The level of INO1 RNA was repressed 12-fold when the cells were grown in medium containing inositol, and it was repressed 33-fold when the cells were grown in the presence of inositol and choline together. The INO1 transcript was present at a very low level in cells containing mutations (ino2 and ino4) in regulatory genes unlinked to INO1 that result in inositol auxotrophy. The transcript was constitutively overproduced in cells containing a mutation (opi1) that causes constitutive expression of inositol-1-phosphate synthase and results in excretion of inositol. The expression of INO1 RNA was also examined in cells containing a mutation (cho2) affecting the synthesis of phosphatidylcholine. In contrast to what was observed in wild-type cells, growth of cho2 cells in medium containing inositol did not result in a significant decrease in INO1 RNA abundance. Inositol and choline together were required for repression of the INO1 transcript in these cells, providing evidence for a regulatory link between the synthesis of inositol- and choline-containing lipids. The level of the 0.6-kb RNA was affected, although to a lesser degree, by many of the same factors that influence INO1 expression.
机译:酿酒酵母的INO1基因编码受调节的肌醇-1-磷酸合酶,催化合成含肌醇磷脂的第一步。在已知调节磷脂合成的条件下分析该基因的表达。与INO1基因组克隆的RNA印迹杂交检测到两个1.8 kb和0.6 kb的RNA。当细胞在磷脂前体肌醇存在下生长时,1.8-kb RNA的丰度大大降低,合酶的酶活性也是如此。互补分析表明该转录物编码了INO1基因产物。当细胞在含有肌醇的培养基中生长时,INO1 RNA的水平被抑制了12倍,而当细胞在肌醇和胆碱的存在下一起生长时,其被抑制了33倍。 INO1转录本在细胞中的含量非常低,该细胞含有与INO1无关的调节基因突变(ino2和ino4),导致肌醇营养缺陷。转录本在包含突变(opi1)的细胞中组成性过量产生,该突变导致肌醇-1-磷酸合酶的组成性表达并导致肌醇排泄。还在包含影响磷脂酰胆碱合成的突变(cho2)的细胞中检查了INO1 RNA的表达。与在野生型细胞中观察到的相反,在含有肌醇的培养基中cho2细胞的生长并未导致INO1 RNA丰度的显着降低。在这些细胞中抑制INO1转录需要肌醇和胆碱,这为肌醇和胆碱的脂质合成之间的调节联系提供了证据。尽管影响程度较小,但影响INO1表达的许多相同因素对0.6-kb RNA的水平影响较小。

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