Wang S M, Chu B, Lue W L, Yu T S, Eimert K, Chen J
Department of Botany, National Taiwan University, Taipei, Taiwan.
Plant J. 1997 May;11(5):1121-6. doi: 10.1046/j.1365-313x.1997.11051121.x.
Arabidopsis mutants affecting ADPG pyrophosphorylase (ADGase) activity can be divided into two complementation groups, adg1 and adg2. Previous biochemical studies of adg2-1 mutant indicated that mutant plants do not accumulate ADGase large subunit protein and that ADGase small subunits assemble as homotetramers. This suggested that the ADG2 gene may encode the large subunit of ADGase. In this paper, it is shown that adg2-1 mutant plants accumulate near wild-type levels of transcripts encoding both the large and small subunits of ADGase. However, by RFLP analysis and complementation of adg2-1 with the ADGase large subunit gene, we show that the adg2-1 mutant does represent a mutation of the ADGase large subunit gene. Sequence analysis of the adg2-1 allele revealed a missense mutation. The results therefore suggest either that the missense mutation affects the stability of the ADGase large subunit protein or that it prevents assembly of the large subunit into holoenzyme.
影响ADP葡萄糖焦磷酸化酶(ADGase)活性的拟南芥突变体可分为两个互补组,即adg1和adg2。先前对adg2 - 1突变体的生化研究表明,突变植株不积累ADGase大亚基蛋白,且ADGase小亚基组装成同四聚体。这表明ADG2基因可能编码ADGase的大亚基。本文表明,adg2 - 1突变植株积累的ADGase大亚基和小亚基转录本水平接近野生型。然而,通过RFLP分析以及用ADGase大亚基基因对adg2 - 1进行互补实验,我们发现adg2 - 1突变体确实代表ADGase大亚基基因的一个突变。对adg2 - 1等位基因的序列分析揭示了一个错义突变。因此,结果表明该错义突变要么影响ADGase大亚基蛋白的稳定性,要么阻止大亚基组装成全酶。