Shatters R G, Kahn M L
Program in Genetics and Cell Biology, Washington State University, Pullman 99164-6340.
J Mol Evol. 1989 Nov;29(5):422-8. doi: 10.1007/BF02602912.
We have determined the DNA sequence of a Rhizobium meliloti gene that encodes glutamine synthetase II (GSII). The deduced amino acid sequence was compared to that of Bradyrhizobium japonicum GSII and those of various plant and mammalian glutamine synthetases (GS) in order to evaluate a proposal that the gene for this enzyme was recently transferred from plants to their symbiotic bacteria. There is 83.6% identity between the R. meliloti and B. japonicum proteins. The bacterial GSII proteins average 42.5% identity with the plant GS proteins and 41.8% identity with their mammalian counterparts. The plant proteins average 53.7% identity with the mammalian proteins. Thus, the GS proteins are highly conserved and the divergence of these proteins is proportional to the phylogenetic divergence of the organisms from which the sequences were determined. No transfer of genes across large taxonomic gaps is needed to explain the presence of GSII in these bacteria.
我们已经测定了编码谷氨酰胺合成酶II(GSII)的苜蓿中华根瘤菌基因的DNA序列。将推导的氨基酸序列与日本慢生根瘤菌GSII的序列以及各种植物和哺乳动物谷氨酰胺合成酶(GS)的序列进行了比较,以便评估关于该酶基因最近从植物转移到其共生细菌的提议。苜蓿中华根瘤菌和日本慢生根瘤菌的蛋白质之间有83.6%的同一性。细菌GSII蛋白质与植物GS蛋白质的平均同一性为42.5%,与哺乳动物对应蛋白质的平均同一性为41.8%。植物蛋白质与哺乳动物蛋白质的平均同一性为53.7%。因此,GS蛋白质高度保守,这些蛋白质的差异与确定序列的生物体的系统发育差异成比例。无需跨大的分类学间隔转移基因来解释这些细菌中GSII的存在。