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Methionine depletion induces transcription of the mRNA (N6-adenosine)methyltransferase.
- Source :
-
The international journal of biochemistry & cell biology [Int J Biochem Cell Biol] 2001 Nov; Vol. 33 (11), pp. 1116-28. - Publication Year :
- 2001
-
Abstract
- This study examines the genetic expression of the S-adenosyl-L-methionine binding subunit of the mRNA (N6-adenosine)methyltransferase (MT-A70) in cultured cells under conditions known to affect transmethylation reactions. Methionine dependence, disrupted methionine metabolism, and increased transmethylation reactions are all phenotypes characteristic of cancer cells. The results show that both methionine depletion and inhibition of S-adenosyl-L-methionine formation can induce up to a four-fold increase in transcription of this S-adenosyl-L-methionine binding subunit. The two splice-variant mRNAs produced from the MT-A70 gene are transcribed at different rates depending on the level of S-adenosyl-L-methionine inhibition. This result may reflect differing Km values toward the substrate for the different enzyme isoforms. 3-Deazaadenosine, an inhibitor known to block certain mRNA transmethylations, was shown to have no effect on MT-A70 gene expression. This result indicates that the control of MT-A70 gene expression is directly related to methionine availability and the subsequent synthesis of S-adenosyl-L-methionine.
- Subjects :
- Animals
Autoradiography
Cycloleucine pharmacology
Ethionine pharmacology
Methionine metabolism
Methionine pharmacology
Mice
Nuclease Protection Assays
RNA, Messenger biosynthesis
RNA, Messenger genetics
RNA, Messenger metabolism
Reverse Transcriptase Polymerase Chain Reaction
Ribonucleases metabolism
Tubercidin pharmacology
Tumor Cells, Cultured
Gene Expression Regulation, Enzymologic drug effects
Methionine deficiency
Methyltransferases genetics
Transcription, Genetic drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1357-2725
- Volume :
- 33
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- The international journal of biochemistry & cell biology
- Publication Type :
- Academic Journal
- Accession number :
- 11551827
- Full Text :
- https://doi.org/10.1016/s1357-2725(01)00072-3