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
-
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
-
Asparaginyl-tRNA and resistance of murine leukaemias to L-asparaginase.
Nature. 1970 Sep 12;227(5263):1134-6
PMID: 5451107
-
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
-
An improved nutrient solution for diploid Chinese hamster and human cell lines.
Exp Cell Res. 1963 Feb;29:515-26
PMID: 13952250
-
ROLE OF VALYL-SRNA SYNTHETASE IN ENZYME REPRESSION.
Proc Natl Acad Sci U S A. 1965 Mar;53:539-43
PMID: 14338232
-
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75
PMID: 14907713
-
Regulation of bacterial ppGpp and pppGpp.
Annu Rev Microbiol. 1975;29:301-18
PMID: 170852
-
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
-
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
-
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
-
Asparagine-requiring tumor cell lines and their non-requiring variants: cytogenetics, biochemistry and population dynamics.
Genetics. 1973 Nov;75(3):503-14
PMID: 4798091
-
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
-
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
-
Two types of ribosome in mouse-hamster hybrid cells.
Nat New Biol. 1971 Mar 10;230(10):52-4
PMID: 5279808
-
Function and regulation of aminoacyl-tRNA synthetases in prokaryotic and eukaryotic cells.
Annu Rev Microbiol. 1975;29:215-50
PMID: 1180514