Thomas D, Cherest H, Surdin-Kerjan Y
Laboratoire d'Enzymologie du CNRS, Gif-sur-Yvette, France.
EMBO J. 1991 Mar;10(3):547-53. doi: 10.1002/j.1460-2075.1991.tb07981.x.
Cloning of the MET19 gene revealed that it encodes the glucose-6-phosphate dehydrogenase from yeast. Sequence analysis showed a high degree of similarity between the yeast and the human enzymes. The cloned gene has allowed the construction of a glucose-6-phosphate dehydrogenase null mutant. The only phenotype of such a strain is an absolute requirement for an organic sulfur source, i.e. methionine, S-adenosylmethionine (AdoMet), cysteine, glutathione or homocysteine. The phenotype of this null mutant raises some new questions about the exact functions of the pentose phosphate pathway which was usually considered as the main cellular source of NADPH. Moreover, results reported here show that an increase of the AdoMet pool represses the transcription of the glucose-6-phosphate dehydrogenase gene. This regulation acts on the glucose-6-phosphate dehydrogenase biosynthesis but does not affect the synthesis of 6-phosphogluconate dehydrogenase. That AdoMet controls a part of the pentose phosphate pathway sheds new light on mechanisms regulating the relative fluxes of carbon utilization through the pentose phosphate pathway and glycolysis.
MET19基因的克隆表明它编码酵母中的葡萄糖-6-磷酸脱氢酶。序列分析显示酵母和人类的这种酶之间有高度的相似性。克隆的基因使得构建葡萄糖-6-磷酸脱氢酶缺失突变体成为可能。这种菌株唯一的表型是对有机硫源(即蛋氨酸、S-腺苷甲硫氨酸(AdoMet)、半胱氨酸、谷胱甘肽或高半胱氨酸)有绝对需求。这种缺失突变体的表型对戊糖磷酸途径的具体功能提出了一些新问题,戊糖磷酸途径通常被认为是细胞内NADPH的主要来源。此外,这里报道的结果表明AdoMet库的增加会抑制葡萄糖-6-磷酸脱氢酶基因的转录。这种调控作用于葡萄糖-6-磷酸脱氢酶的生物合成,但不影响6-磷酸葡萄糖酸脱氢酶的合成。AdoMet控制戊糖磷酸途径的一部分,这为调节通过戊糖磷酸途径和糖酵解的碳利用相对通量的机制提供了新的线索。