CLONING AND CHARACTERIZATION OF CDNA-ENCODING A HUMAN ARGINYL-TRANSFER-RNA SYNTHETASE

被引:14
作者
GIRJES, AA
HOBSON, K
CHEN, P
LAVIN, MF
机构
[1] QUEENSLAND INST MED RES, BANCROFT CTR, QUEENSLAND CANC FUND RES UNIT, BRISBANE, QLD 4029, AUSTRALIA
[2] UNIV QUEENSLAND, DEPT ANAT SCI, ST LUCIA, QLD 4067, AUSTRALIA
[3] UNIV QUEENSLAND, DEPT SURG, BRISBANE, QLD 4029, AUSTRALIA
关键词
RECOMBINANT DNA; PROTEIN SYNTHESIS; HOMOLOGIES; ATAXIA TELANGIECTASIA; FULL-LENGTH CDNA; DNA SEQUENCING; NORTHERN BLOT;
D O I
10.1016/0378-1119(95)00502-W
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Arginyl-tRNA synthetase (ArgRS) plays a key role in protein synthesis as part of a multienzyme complex with a number of other aminoacyl-tRNA synthetase (aaRS) enzymes. We have isolated a full-length cDNA encoding ArgRS as part of a project on complementation of radiosensivity in human cells with an Epstein-Barr Virus (EBV) vector-based human cDNA library. DNA sequence analysis identified an open reading frame of 1983 nucleotides with 87% homology to other mammalian ArgRS genes, The deduced amino acid (aa) sequence (661 aa) showed 87.7% identity to the Chinese hamster ovary (CHO) enzyme and 37.7% identity to the homologous Escherichia coli enzyme. Northern blot analysis revealed the presence of a single mRNA species of approx. 2.2 kb. The results described here demonstrate that ArgRS is highly conserved in mammalian cells and confirm the presence of a hydrophobic N-terminal region in the higher-molecular-weight complexed form of ArgRS.
引用
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页码:347 / 350
页数:4
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