Abstract
9-β-D-Arabinofuranosyladenine 5′-monophosphate (araAMP) is more lethal to mouse fibroblasts (L cells) than the identical exogenous concentration of 9-β-D-arabinofuranosyladenine (araA) (Cancer Res. 32, 1512, 1972). [3H,32P]AraAMP (0.1 mM) was taken into L cells for 4 hr in the presence of a large excess of 32Pi. The radioactivity was subsequently found mainly in the adenine nucleotides in the acid-soluble fraction and in the cell DNA. The cellular concentration of 9-β-D-arabinofuranosyladenine 5′-triphosphate (araATP) exceeded 2 μM. More than 90% of the 3H was associated with araA in the nucleotides. After degradation of the adenine-containing triphosphates with apyrase, the adenine mononucleotides were separated by thin-layer electrophoresis and chromatography. All of the 32P and 97% of the 3H were associated with araAMP.
The small amounts of 3H and 32P in the acid-insoluble material were similar during a 4 hr incubation. The DNA fraction was degraded enzymatically to 5′-mononucleotides. Both 32P and 3H were associated predominantly with 5′-dAMP. Most of the 3H was in araA, detected after dephosphorylation. Enzymatic degradation of the DNA fraction to 3′-mononucleotides and fractionation revealed 3H primarily in the 3′-adenine nucleotide and 32P in each of the deoxynucleoside 3′-monophosphates. After dephosphorylation of the 3′-mononucleotides, 93% of the 3H was found in araA. These results suggest that small amounts of araAMP penetrated the cell as an intact nucleotide, were further phosphorylated to the triphosphate, and subsequently incorporated in internucleotide linkage into DNA.
Keywords: penetrability, nucleotides, araA, araAMP, araATP
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cohen S. S. Introduction to the biochemistry of D-arabinosyl nucleosides. Prog Nucleic Acid Res Mol Biol. 1966;5:1–88. doi: 10.1016/s0079-6603(08)60231-7. [DOI] [PubMed] [Google Scholar]
- Doering A. M., Jansen M., Cohen S. S. Polymer synthesis in killed bacteria: lethality of 2',3'-dideoxyadenosine. J Bacteriol. 1966 Sep;92(3):565–574. doi: 10.1128/jb.92.3.565-574.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doering A., Keller J., Cohen S. S. Some effects of D-arabinosyl nucleosides on polymer syntheses in mouse fibroblasts. Cancer Res. 1966 Dec;26(12):2444–2450. [PubMed] [Google Scholar]
- Furth J. J., Cohen S. S. Inhibition of mammalian DNA polymerase by the 5'-triphosphate of 1-beta-d-arabinofuranosylcytosine and the 5'-triphosphate of 9-beta-d-arabinofuranoxyladenine. Cancer Res. 1968 Oct;28(10):2061–2067. [PubMed] [Google Scholar]
- Furth J. J., Cohen S. S. Inhibition of mammalian DNA polymerase by the 5'-triphosphate of 9-beta-D-arabinofuranosyladenine. Cancer Res. 1967 Sep;27(9):1528–1533. [PubMed] [Google Scholar]
- LEIBMAN K. C., HEIDELBERGER C. The metabolism of P32-labeled ribonucleotides in tissue slices and cell suspensions. J Biol Chem. 1955 Oct;216(2):823–830. [PubMed] [Google Scholar]
- LICHTENSTEIN J., BARNER H. D., COHEN S. S. The metabolism of exogenously supplied nucleotides by Escherichia coli. J Biol Chem. 1960 Feb;235:457–465. [PubMed] [Google Scholar]
- LePage G. A. Arabinosyladenine and arabinosylhypoxanthine metabolism in murine tumor cells. Can J Biochem. 1970 Jan;48(1):75–78. doi: 10.1139/o70-013. [DOI] [PubMed] [Google Scholar]
- LePage G. A., Hersh E. M. Cyclic nucleotide analogs as carcinostatic agents. Biochem Biophys Res Commun. 1972 Mar 10;46(5):1918–1922. doi: 10.1016/0006-291x(72)90070-8. [DOI] [PubMed] [Google Scholar]
- Moore E. C., Cohen S. S. Effects of arabinonucleotides on ribonucleotide reduction by an enzyme system from rat tumor. J Biol Chem. 1967 May 10;242(9):2116–2118. [PubMed] [Google Scholar]
- Ortiz P. J., Manduka M. J., Cohen S. S. The lethality of some D-arabinosyl nucleotides to mouse fibroblasts. Cancer Res. 1972 Jul;32(7):1512–1517. [PubMed] [Google Scholar]
- ROLL P. M., WEINFELD H., CARROLL E., BROWN G. B. The utilization of nucleotides by the mammal. IV. Triply labeled purine nucleotides. J Biol Chem. 1956 May;220(1):439–454. [PubMed] [Google Scholar]
- ROLL P. M., WEINFELD H., CARROLL E. The utilization of nucleotides by the mammal. V. Metabolism of pyrimidine nucleotides. J Biol Chem. 1956 May;220(1):455–465. [PubMed] [Google Scholar]
- Ryan W. L., Durick M. A. Adenosine 3',5'-monophosphate and N 6 -2'-O-dibutyryl-adenosine 3',5'-monophosphate transport in cells. Science. 1972 Sep 15;177(4053):1002–1003. doi: 10.1126/science.177.4053.1002. [DOI] [PubMed] [Google Scholar]
- Toji L., Cohen S. S. Termination of deoxyribonucleic acid in Escherichia coli by 2',3'-dideoxyadenosine. J Bacteriol. 1970 Aug;103(2):323–328. doi: 10.1128/jb.103.2.323-328.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waqar M. A., Burgoyne L. A., Atkinson M. R. Deoxyribonucleic acid synthesis in mammalian nuclei. Incorporation of deoxyribonucleotides and chain-terminating nucleotide analogues. Biochem J. 1971 Mar;121(5):803–809. doi: 10.1042/bj1210803. [DOI] [PMC free article] [PubMed] [Google Scholar]
