Home LiteratureArticle Details
PMID: 7962006 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human glycyl-tRNA synthetase. Wide divergence of primary structure from bacterial counterpart and species-specific aminoacylation.

The Journal of biological chemistry ·Vol. 269 ·No. 47 ·1994-11-25 ·Pages 30049-55

Shiba K, Schimmel P, Motegi H, Noda T

Abstract

Several class I and class II human tRNA synthetases are clearly related to their bacterial counterparts. We report here the cloning, cDNA sequence, deduced primary structure, and expression in bacteria of a class II human glycyl-tRNA synthetase. While the human sequence aligns well with a Bombyx mori and a Saccharomyces cerevisiae sequence for glycyl-tRNA synthetase, particularly in the region of the class II-defining sequence motifs, it diverges widely from that of the Escherichia coli enzyme. The divergence is so great that from the sequences alone we cannot conclude that the human and E. coli proteins are descended from homologous genes. Moreover, even though the human and E. coli class II alanyl-tRNA synthetases cross-acylate their respective tRNAs, aminoacylations by the recombinant human and E. coli glycyl-tRNA synthetases are restricted to their homologous tRNAs. The species-specific aminoacylations correlate with a nucleotide sequence difference at a location in the acceptor stem that is known to be critical for aminoacylations by the E. coli enzyme. Thus, glycyl-tRNA synthetase may have followed a path of historical development different in at least some respects from that of several other tRNA synthetases.

MeSH Terms
Acylation Amines Amino Acid Sequence Animals Bombyx/enzymology Cells, Cultured Escherichia coli/enzymology Glycine-tRNA Ligase/chemistry Humans Molecular Sequence Data Polymerase Chain Reaction Saccharomyces cerevisiae/enzymology Sequence Homology, Amino Acid Species Specificity
Chemicals
Amines Glycine-tRNA Ligase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shiba K
Department of Cell Biology, Japanese Foundation for Cancer Research, Tokyo.
Schimmel P
Motegi H
Noda T
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1994-11-25
Pages
30049-55
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM23562 · United States
Databases
GENBANK
D30658
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com