Wasilenko Jamie, Fridovich-Keil Judith L
Graduate Program in Genetics and Molecular Biology, Emory University and Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Biol Chem. 2006 Mar 31;281(13):8443-9. doi: 10.1074/jbc.M600778200. Epub 2006 Feb 1.
UDP-galactose 4'-epimerase (GALE) catalyzes the final step of the highly conserved Leloir pathway of galactose metabolism. Loss of GALE in humans results in a variant form of the metabolic disorder, galactosemia. Loss of GALE in yeast results in galactose-dependent growth arrest. Although the role of GALE in galactose metabolism has been recognized for decades, the precise relationship between GALE activity and galactose sensitivity has remained unclear. Here we have explored this relationship by asking the following. 1) Is GALE rate-limiting for galactose metabolism in yeast? 2) What is the relationship between GALE activity and galactose-dependent growth arrest in yeast? 3) What is the relationship between GALE activity and the abnormal accumulation of galactose metabolites in yeast? To answer these questions we engineered a strain of yeast in which GALE was doxycycline-repressible and studied these cells under conditions of intermediate GALE expression. Our results demonstrated a smooth linear relationship between galactose metabolism and GALE activity over a range from 0 to approximately 5% but a steep threshold relationship between growth rate in galactose and GALE activity over the same range. The relationship between abnormal accumulation of metabolites and GALE activity was also linear over the range from 0 to approximately 5%, suggesting that if the abnormal accumulation of metabolites underlies galactose-dependent growth-arrest in GALE-impaired yeast, either the impact of individual metabolites must be synergistic and/or the threshold of sensitivity must be very steep. Together these data reveal important points of similarity and contrast between the roles of GALE and galactose-1-phosphate uridylyltransferase in galactose metabolism in yeast and provide a framework for future studies in mammalian systems.
UDP-半乳糖4'-表异构酶(GALE)催化半乳糖代谢高度保守的勒洛伊尔途径的最后一步。人类中GALE的缺失会导致一种代谢紊乱的变体形式——半乳糖血症。酵母中GALE的缺失会导致半乳糖依赖性生长停滞。尽管几十年来人们已经认识到GALE在半乳糖代谢中的作用,但GALE活性与半乳糖敏感性之间的确切关系仍不清楚。在这里,我们通过提出以下问题来探索这种关系。1)GALE对酵母中的半乳糖代谢是否具有限速作用?2)GALE活性与酵母中半乳糖依赖性生长停滞之间的关系是什么?3)GALE活性与酵母中半乳糖代谢物异常积累之间的关系是什么?为了回答这些问题,我们构建了一种酵母菌株,其中GALE可被强力霉素抑制,并在中等GALE表达条件下研究这些细胞。我们的结果表明,在0至约5%的范围内,半乳糖代谢与GALE活性之间存在平滑的线性关系,但在相同范围内,半乳糖中的生长速率与GALE活性之间存在陡峭的阈值关系。代谢物异常积累与GALE活性之间的关系在0至约5%的范围内也是线性的,这表明如果代谢物的异常积累是GALE受损酵母中半乳糖依赖性生长停滞的基础,那么要么单个代谢物的影响必须是协同的,要么敏感性阈值必须非常陡峭。这些数据共同揭示了GALE和1-磷酸半乳糖尿苷酰转移酶在酵母半乳糖代谢中的作用之间重要的异同点,并为未来在哺乳动物系统中的研究提供了框架。