Peterman T K, Goodman H M
Department of Genetics, Harvard Medical School, Boston, MA.
Mol Gen Genet. 1991 Nov;230(1-2):145-54. doi: 10.1007/BF00290662.
Glutamine synthetase (GS) plays an important role in the assimilation of nitrogen by higher plants. We present here a molecular analysis of the GS polypeptides, mRNAs, and genes of Arabidopsis thaliana. Western blot analysis of leaf and root protein extracts revealed at least two distinct GS polypeptides; 43 kDa and 39 kDa GS polypeptides were present in leaves, while only a 39 kDa GS was detected in roots. The 43 kDa GS polypeptide is light-inducible. In etiolated seedlings only the 39 kDa GS was detected. However, upon greening the 43 kDa GS increased to levels comparable to those observed in light-grown plants. Four distinct GS cDNA clones, lambda Atgsl1, lambda Atgsr1, lambda Atgsr2 and lambda Atkb6 were isolated and characterized. Their complete nucleotide and deduced amino acid sequences are presented. The coding sequences of the four clones are 70-88% similar while their 5' and 3' untranslated regions exhibit less than 50% similarity. Northern blots of leaf, root and germinated seed RNA revealed that the four cDNAs hybridize to mRNAs which are differentially expressed in the organs of Arabidopsis thaliana. lambda Atgsl1 is leaf-specific and hybridizes to a 1.6 kb mRNA. Both lambda Atgsr1 and lambda Atgskb6 hybridize to 1.4 kb mRNAs which are expressed in both roots and germinated seeds. lambda Atgsr2 hybridizes to a 1.4 kb mRNA, which is primarily expressed in roots with low levels of expression in seeds and leaves. lambda Atgsl1, which represents the leaf-specific mRNA, is induced by light. lambda Atgsl1 mRNA levels increase during the greening of etiolated seedlings while lambda Atgsr1 levels remain constant. Southern blot analysis indicated that the Arabidopsis genome contains at least four and possibly five distinct GS genes.
谷氨酰胺合成酶(GS)在高等植物的氮同化过程中发挥着重要作用。我们在此展示了对拟南芥GS多肽、mRNA和基因的分子分析。对叶片和根蛋白提取物的蛋白质免疫印迹分析显示至少有两种不同的GS多肽;叶片中存在43 kDa和39 kDa的GS多肽,而根中仅检测到39 kDa的GS。43 kDa的GS多肽是光诱导的。在黄化幼苗中仅检测到39 kDa的GS。然而,在绿化后,43 kDa的GS增加到与在光照生长的植物中观察到的水平相当。分离并鉴定了四个不同的GS cDNA克隆,λAtgsl1、λAtgsr1、λAtgsr2和λAtkb6。展示了它们完整的核苷酸和推导的氨基酸序列。四个克隆的编码序列相似度为70 - 88%,而它们的5'和3'非翻译区的相似度低于50%。对叶片、根和萌发种子RNA的Northern印迹分析表明,这四个cDNA与在拟南芥器官中差异表达的mRNA杂交。λAtgsl1是叶片特异性的,与1.6 kb的mRNA杂交。λAtgsr1和λAtgskb6都与1.4 kb的mRNA杂交,这些mRNA在根和萌发种子中都有表达。λAtgsr2与1.4 kb的mRNA杂交,该mRNA主要在根中表达,在种子和叶片中的表达水平较低。代表叶片特异性mRNA的λAtgsl1受光诱导。在黄化幼苗绿化过程中,λAtgsl1 mRNA水平增加,而λAtgsr1水平保持不变。Southern印迹分析表明,拟南芥基因组至少包含四个,可能五个不同的GS基因。