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PMID: 18735 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

A role for asparaginyl-tRNA in the regulation of asparagine synthetase in a mammalian cell line.

Arfin SM, Simpson DR, Chiang CS, Andrulis IL, Hatfield GW

Abstract

The expression of asparagine synthetase activity [L-aspartate:ammonia ligase (AMP-forming), EC 6.3.1.1] in cultured Chinese hamster ovary (CHO) cells is regulated by asparagine. After transfer of CHO cells from an asparagine-supplemented medium to a medium lacking asparagine, activity increases 1.5- to 2-fold. If asparagine is added back to the medium, activity returns to control levels. To test the possible involvement of Asn-tRNAAsn in regulating the levels of asparagine synthetase, we have examined the levels of asparagine synthetase in a mutant of CHO cells containing a temperature-sensitive asparaginyl-tRNA synthetase [L-asparagine:tRNA ligase (AMP-forming), EC 6.1.1.22]. Under conditions of limited asparaginyl-tRNA synthetase activity in the mutant, there is a 2- to 3-fold increase in the level of asparagine synthetase activity. Under identical conditions, there is no change in asparagine synthetase activity in the wild type. This correlation between asparaginyl-tRNA synthetase activity and asparagine synthetase levels may be a consequence of a direct role of tRNAAsn in the regulation of the in vivo expression of the asparagine synthetase structural gene.

MeSH Terms
Asparagine/pharmacology Aspartate-Ammonia Ligase/metabolism Cell Line Enzyme Induction/drug effects Feedback Kinetics Ligases/metabolism RNA, Transfer/physiology Temperature
Chemicals
Asparagine RNA, Transfer Ligases Aspartate-Ammonia Ligase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Arfin S M
Simpson D R
Chiang C S
Andrulis I L
Hatfield G W
References (15)
15 references, click to expand
  1. Role of leucyl-tRNA synthetase in regulation of branched-chain amino-acid transport.
    Proc Natl Acad Sci U S A. 1975 Oct;72(10):3921-4 PMID: 1105569
  2. Asparaginyl-tRNA and resistance of murine leukaemias to L-asparaginase.
    Nature. 1970 Sep 12;227(5263):1134-6 PMID: 5451107
  3. Selection by [3H] amino acids of CHO-cell mutants with altered leucyl- and asparagyl-transfer RNA synthetases.
    Somatic Cell Genet. 1975 Apr;1(2):187-208 PMID: 1235906
  4. An improved nutrient solution for diploid Chinese hamster and human cell lines.
    Exp Cell Res. 1963 Feb;29:515-26 PMID: 13952250
  5. ROLE OF VALYL-SRNA SYNTHETASE IN ENZYME REPRESSION.
    Proc Natl Acad Sci U S A. 1965 Mar;53:539-43 PMID: 14338232
  6. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  7. Regulation of bacterial ppGpp and pppGpp.
    Annu Rev Microbiol. 1975;29:301-18 PMID: 170852
  8. A comparison of kinetic parameters obtained with three major non-interconvertible isozymes of rat pyruvate kinase.
    Arch Biochem Biophys. 1973 Jun;156(2):730-44 PMID: 4352423
  9. A mammalian cell mutant with a temperature-sensitive leucyl-transfer RNA synthetase.
    Proc Natl Acad Sci U S A. 1973 Nov;70(11):3094-8 PMID: 4361675
  10. Enzymatic and nutritional evidence for two-stage exression of the asparagine synthetase locus in L5178y murine leukemia mutants.
    Cancer Res. 1974 Nov;34(11):2940-5 PMID: 4529293
  11. Asparagine-requiring tumor cell lines and their non-requiring variants: cytogenetics, biochemistry and population dynamics.
    Genetics. 1973 Nov;75(3):503-14 PMID: 4798091
  12. Glutamine-dependent asparagine synthetase from leukemia cells. Chloride dependence, mechanism of action, and inhibition.
    J Biol Chem. 1972 Oct 25;247(20):6708-19 PMID: 5076775
  13. A role of aminoacyl-tRNA in the regulation of protein breakdown in Escherichia coli.
    Proc Natl Acad Sci U S A. 1971 Feb;68(2):362-6 PMID: 5277086
  14. Two types of ribosome in mouse-hamster hybrid cells.
    Nat New Biol. 1971 Mar 10;230(10):52-4 PMID: 5279808
  15. Function and regulation of aminoacyl-tRNA synthetases in prokaryotic and eukaryotic cells.
    Annu Rev Microbiol. 1975;29:215-50 PMID: 1180514
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1977-06-00
Pages
2367-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC432172
Subset
IM
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