Quettier Anne-Laure, Shaw Eve, Eastmond Peter J
Warwick HRI, University of Warwick, Wellesbourne, Warwickshire CV35 9EF, United Kingdom.
Plant Physiol. 2008 Sep;148(1):519-28. doi: 10.1104/pp.108.123703. Epub 2008 Jul 3.
The aim of this study was to clone and characterize the SUGAR-DEPENDENT6 (SDP6) gene, which is essential for postgerminative growth in Arabidopsis (Arabidopsis thaliana). Mutant alleles of sdp6 were able to break down triacylglycerol following seed germination but failed to accumulate soluble sugars, suggesting that they had a defect in gluconeogenesis. Map-based cloning of SDP6 revealed that it encodes a mitochondrial flavin adenine dinucleotide (FAD)-dependent glycerol-3-P (G3P) dehydrogenase:ubiquinone oxidoreductase called FAD-GPDH. This gene has previously been proposed to play a role both in the break down of glycerol (derived from triacylglycerol) and in NAD(+)/NADH homeostasis. Germinated seeds of sdp6 were severely impaired in the metabolism of [U-(14)C]glycerol to CO(2) and accumulated high levels of G3P. These data suggest that SDP6 is essential for glycerol catabolism. The activity of the glycolytic enzyme phosphoglucose isomerase is competitively inhibited by G3P in vitro. We show that phosphoglucose isomerase is likely to be inhibited in vivo because there is a 6-fold reduction in the transfer of (14)C-label into the opposing hexosyl moiety of sucrose when [U-(14)C]glucose or [U-(14)C]fructose is fed to sdp6 seedlings. A block in gluconeogenesis, at the level of hexose phosphate isomerization, would account for the arrested seedling growth phenotype of sdp6 and explain its rescue by sucrose and glucose but not by fructose. Measurements of NAD(+) and NADH levels in sdp6 seedlings also suggest that NAD(+)/NADH homeostasis is altered, and this observation is consistent with the hypothesis that SDP6 participates in a mitochondrial G3P shuttle by cooperating with the cytosolic NAD-dependent GPDH protein GPDHC1.
本研究的目的是克隆并鉴定拟南芥(Arabidopsis thaliana)中对种子萌发后生长至关重要的糖依赖6(SUGAR-DEPENDENT6,SDP6)基因。sdp6的突变等位基因在种子萌发后能够分解三酰甘油,但无法积累可溶性糖,这表明它们在糖异生过程中存在缺陷。对SDP6进行图位克隆发现,它编码一种线粒体黄素腺嘌呤二核苷酸(FAD)依赖性甘油-3-磷酸(G3P)脱氢酶:泛醌氧化还原酶,称为FAD-GPDH。此前有研究提出该基因在甘油(源自三酰甘油)的分解以及NAD(+)/NADH稳态维持中均发挥作用。sdp6的萌发种子在将[U-(14)C]甘油代谢为CO(2)的过程中严重受损,并积累了高水平的G3P。这些数据表明SDP6对甘油分解代谢至关重要。在体外,糖酵解酶磷酸葡萄糖异构酶的活性受到G3P的竞争性抑制。我们发现,磷酸葡萄糖异构酶在体内可能也受到抑制,因为当给sdp6幼苗喂食[U-(14)C]葡萄糖或[U-(14)C]果糖时,(14)C标记向蔗糖相反己糖部分的转移减少了6倍。在磷酸己糖异构化水平上的糖异生受阻,将解释sdp6幼苗生长停滞的表型,并说明其可被蔗糖和葡萄糖而非果糖拯救的原因。对sdp6幼苗中NAD(+)和NADH水平的测量还表明,NAD(+)/NADH稳态发生了改变,这一观察结果与SDP6通过与胞质NAD依赖性GPDH蛋白GPDHC1合作参与线粒体G3P穿梭的假说一致。