Flores Carmen-Lisset, Gancedo Carlos
Instituto de Investigaciones Biomédicas Alberto Sols, CSIC-Universidad Autónoma de Madrid, Madrid, Spain.
Eukaryot Cell. 2005 Feb;4(2):356-64. doi: 10.1128/EC.4.2.356-364.2005.
We have cloned and characterized the gene PYC1, encoding the unique pyruvate carboxylase in the dimorphic yeast Yarrowia lipolytica. The protein putatively encoded by the cDNA has a length of 1,192 amino acids and shows around 70% identity with pyruvate carboxylases from other organisms. The corresponding genomic DNA possesses an intron of 269 bp located 133 bp downstream of the starting ATG. In the branch motif of the intron, the sequence CCCTAAC, not previously found at this place in spliceosomal introns of Y. lipolytica, was uncovered. Disruption of the PYC1 gene from Y. lipolytica did not abolish growth in glucose-ammonium medium, as is the case in other eukaryotic microorganisms. This unusual growth phenotype was due to an incomplete glucose repression of the function of the glyoxylate cycle, as shown by the lack of growth in that medium of double pyc1 icl1 mutants lacking both pyruvate carboxylase and isocitrate lyase activity. These mutants grew when glutamate, aspartate, or Casamino Acids were added to the glucose-ammonium medium. The cDNA from the Y. lipolytica PYC1 gene complemented the growth defect of a Saccharomyces cerevisiae pyc1 pyc2 mutant, but introduction of either the S. cerevisiae PYC1 or PYC2 gene into Y. lipolytica did not result in detectable pyruvate carboxylase activity or in growth on glucose-ammonium of a Y. lipolytica pyc1 icl1 double mutant.
我们已经克隆并鉴定了基因PYC1,该基因编码解脂耶氏酵母(Yarrowia lipolytica)中独特的丙酮酸羧化酶。cDNA推定编码的蛋白质长度为1192个氨基酸,与其他生物的丙酮酸羧化酶具有约70%的同一性。相应的基因组DNA在起始ATG下游133 bp处有一个269 bp的内含子。在内含子的分支基序中,发现了序列CCCTAAC,该序列在解脂耶氏酵母剪接体内含子的这个位置之前未曾发现。与其他真核微生物不同,解脂耶氏酵母PYC1基因的破坏并没有消除在葡萄糖 - 铵培养基中的生长。这种不寻常的生长表型是由于乙醛酸循环功能的葡萄糖阻遏不完全,这一点由缺乏丙酮酸羧化酶和异柠檬酸裂解酶活性的双突变体pyc1 icl1在该培养基中无法生长所表明。当向葡萄糖 - 铵培养基中添加谷氨酸、天冬氨酸或酪蛋白氨基酸时,这些突变体能够生长。解脂耶氏酵母PYC1基因的cDNA弥补了酿酒酵母(Saccharomyces cerevisiae)pyc1 pyc2突变体的生长缺陷,但将酿酒酵母的PYC1或PYC2基因导入解脂耶氏酵母中,并未导致可检测到的丙酮酸羧化酶活性,也未使解脂耶氏酵母pyc1 icl1双突变体在葡萄糖 - 铵培养基上生长。