Centre for Plant Molecular Biology, Department of Biology, McGill University, 1205 Docteur Penfield Avenue, Montreal, Canada H3A 1B1.
EMBO J. 1987 May;6(5):1167-71. doi: 10.1002/j.1460-2075.1987.tb02350.x.
Glutamine synthetase is the key enzyme in the assimilation by plants of reduced nitrogen provided from either the soil or fixed symbiotically in association with Rhizobium. We have isolated a number of cDNA clones for soybean glutamine synthetase (GS) from a nodule-cDNA library, using RNA from polysomes immunoprecipitated by GS antibodies. Transcripts corresponding to two clones differing in their 3' non-translated sequences were present in both root and nodule tissue; however, the concentration in the nodules was several times higher. The relative concentrations of these sequences in both tissues is about 9:1. Availability of ammonium ions [provided as NH(4)NO(3) or (NH(4))(2)SO(4)] enhanced the expression of both sequences in root tissue within 2 h, reaching a level similar to that in nodules by 8 h, while KNO(3) had no effect during this period. When nitrogen fixation was prevented by replacing nitrogen with argon in the root environment or when the nodules were formed by a Fix mutant of Bradyrhizobium japonicum, the amounts of GS mRNA did not increase over that in roots. These experiments, together with the time course of increase in GS mRNA transcripts, suggest that the genes encoding cytosolic GS are directly induced by the available ammonia.
谷氨酰胺合成酶是植物同化来自土壤或与根瘤菌共生固定的还原态氮的关键酶。我们使用 GS 抗体免疫沉淀多核糖体 RNA ,从根瘤 cDNA 文库中分离了一些大豆谷氨酰胺合成酶(GS)的 cDNA 克隆。两种 3'非翻译序列不同的克隆的转录本存在于根和根瘤组织中;然而,根瘤中的浓度要高几倍。这两种组织中这些序列的相对浓度约为 9:1。在 2 小时内,铵离子(提供 NH4NO3 或 (NH4)2SO4)的可用性增强了根组织中这两个序列的表达,在 8 小时内达到与根瘤相似的水平,而在这段时间内 KNO3 没有影响。当用氩气代替根环境中的氮来阻止氮固定,或者当根瘤由日本根瘤菌的 Fix 突变体形成时,GS mRNA 的量不会超过根中的量。这些实验,以及 GS mRNA 转录本增加的时间过程,表明编码胞质谷氨酰胺合成酶的基因直接被可用的氨诱导。