Hiesinger M, Wagner C, Schüller H J
Institut für Mikrobiologie, Biochemie und Genetik, Lehrstuhl Biochemie, Universität Erlangen/Nürnberg, Erlangen, Germany.
FEBS Lett. 1997 Sep 22;415(1):16-20. doi: 10.1016/s0014-5793(97)01085-5.
The yeast Saccharomyces cerevisiae contains two acetyl-CoA synthetase genes, ACS1 and ACS2. While ACS1 transcription is glucose repressible, ACS2 shows coregulation with structural genes of fatty acid biosynthesis. The ACS2 upstream region contains an ICRE (inositol/choline-responsive element) as an activating sequence and requires the regulatory genes INO2 and INO4 for maximal expression. We demonstrate in vitro binding of the heterodimeric activator protein Ino2p/Ino4p to the ACS2 promoter. In addition, the pleiotropic transcription factor Abf1p also binds to the ACS2 control region. The identification of ACS2 activating elements also found upstream of ACC1, FAS1 and FAS2 suggests a role of this acetyl-CoA synthetase isoenzyme for the generation of the acetyl-CoA pool required for fatty acid biosynthesis.
酿酒酵母含有两个乙酰辅酶A合成酶基因,ACS1和ACS2。虽然ACS1的转录受葡萄糖抑制,但ACS2与脂肪酸生物合成的结构基因表现出共同调控。ACS2上游区域包含一个ICRE(肌醇/胆碱反应元件)作为激活序列,并且需要调控基因INO2和INO4才能实现最大表达。我们证明了异二聚体激活蛋白Ino2p/Ino4p与ACS2启动子的体外结合。此外,多效转录因子Abf1p也与ACS2调控区域结合。在ACC1、FAS1和FAS2上游也发现了ACS2激活元件,这表明这种乙酰辅酶A合成酶同工酶在脂肪酸生物合成所需的乙酰辅酶A池的生成中发挥作用。