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The cloning and nucleotide sequence of cDNA for an amplified glutamine synthetase gene from the Chinese hamster

机译:中国仓鼠扩增的谷氨酰胺合成酶基因cDNA的克隆与核苷酸序列

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摘要

The nucleotide sequence for a glutamine synthetase (GS) mRNA from gene-amplified Chinese hamster (CHO) cells was determined from recombinant cDNA clones obtained from both pBR322 and λgt10 libraries and by primer extension. The sequence obtained contains about 1400 bp corresponding to a minor species of mRNA terminated by a poly A sequence. The mRNA contains 146 nucleotides of 5′-noncoding region, 1119 bp of coding sequence, and 108 bp of 3′-noncoding sequence with a 32 bp poly(A) tail. The polyadenylation site used shows little homology with efficient polyadenylation sites, but has considerable complementarity with U4 RNA. The predicted amino acid sequence, starting from an initiation codon with the preferred sequence surrounding it, indicates that Chinese hamster GS has high homology with published bovine brain GS peptides and enabled an ordering of these peptides. There is homology between the mammalian GS enzymes and glutamine synthetases obtained from plants and cyanobacteria but no obvious homology between the CHO cell GS sequence and that of other ATP hydrolysing enzymes.
机译:根据从pBR322和λgt10文库中获得的重组cDNA克隆并通过引物延伸,确定了基因扩增的中国仓鼠(CHO)细胞的谷氨酰胺合成酶(GS)mRNA的核苷酸序列。所获得的序列含有约1400bp,其对应于由polyA序列终止的少数mRNA。 mRNA包含146个5'-非编码区核苷酸,1119 bp编码序列和108 bp 3'-非编码序列和32 bp poly(A)尾巴。所使用的聚腺苷酸化位点与有效的聚腺苷酸化位点几乎没有同源性,但是与U4 RNA具有相当的互补性。从起始密码子及其周围的优选序列开始的预测氨基酸序列表明,中国仓鼠GS与已发表的牛脑GS肽具有高度同源性,并能够对这些肽进行排序。从植物和蓝细菌获得的哺乳动物GS酶和谷氨酰胺合成酶之间具有同源性,但是CHO细胞GS序列与其他ATP水解酶之间没有明显的同源性。

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