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PMID: 6102991 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Chinese hamster ovary cells resistant to beta-aspartylhydroxamate contain increased levels of asparagine synthetase.

The Journal of biological chemistry ·Vol. 255 ·No. 10 ·1980-05-25 ·Pages 4808-13

Gantt JS, Chiang CS, Hatfield GW, Arfin SM

Abstract

The growth of Chinese hamster ovary cells in a complete medium lacking asparagine is inhibited by beta-aspartylhydroxamate. The inhibition is overcome by the presence of asparagine in the growth medium. beta-Aspartylhydroxamate inhibits the activity of both asparagine synthetase and asparaginyl-tRNA synthetase in vitro. beta-Aspartylhydroxamate-resistant clones of Chinese hamster ovary cells have been isolated and three of these have been characterized. One clone, AH12, is 3-fold more resistant to beta-aspartylhydroxamate than the parental line and has 2 times higher levels of asparagine synthetase activity. Strains AH2 and AH5 are 6- to 7-fold more resistant to beta-aspartylhydroxamate and have 5 times higher levels of asparagine synthetase. The regulation of the expression of asparagine synthetase is altered in all three resistant cell lines. Whereas asparagine synthetase activity varies 2- to 3-fold in response to the asparagine content of the medium or to the extent of aminoacylation of tRNALeu in the parental cells, the activity of asparagine synthetase in the resistant cells is elevated under all growth conditions. No significant changes in the Km for substrates, Ki for beta-aspartylhydroxamate, or thermal stability were found for the asparagine synthetase of the resistant cells. These variants should prove useful in understanding the mechanisms involved in regulating the levels of asparagine synthetase in mammalian cells.

MeSH Terms
Amino Acyl-tRNA Synthetases/metabolism Animals Asparagine/analogs & derivatives,metabolism,pharmacology Aspartate-Ammonia Ligase/metabolism Aspartate-tRNA Ligase Cell Division/drug effects Cell Line Cricetinae Cricetulus Dose-Response Relationship, Drug Drug Resistance Female Genetic Variation Ligases/metabolism Mutation Ovary RNA, Transfer, Amino Acyl
Chemicals
RNA, Transfer, Amino Acyl beta-aspartylhydroxamic acid Asparagine Ligases Amino Acyl-tRNA Synthetases Aspartate-tRNA Ligase asparaginyl-tRNA synthetase Aspartate-Ammonia Ligase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gantt J S
Chiang C S
Hatfield G W
Arfin S M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1980-05-25
Pages
4808-13
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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