Abstract
Terminal transferase (TdT), when incubated with a purified(32)P-5"-end-labeled oligonucleotide of defined length in the presence of Co(2+), Mn(2+)or Mg(2+)and 2-mercaptoethanol in cacodylate or HEPES buffer, pH 7.2, exhibits the ability to remove a 3"-nucleotide from one oligonucleotide and add it to the 3"-end of another. When analyzed by urea-PAGE, this activity is observed as a disproportionation of the starting oligonucleotide into a ladder of shorter and longer oligonucleotides distributed around the starting material. Optimal metal ion concentration is 1-2 mM. All three metal ions support this activity with Co(2+)> Mn(2+) congruent with Mg(2+). Oligonucleotides p(dT) and p(dA) are more efficient substrates than p(dG) and p(dC) because the latter may form secondary structures. The dismutase activity is significant even in the presence of dNTP concentrations comparable to those that exist in the nucleus during the G(1)phase of the cell cycle. Using BetaScope image analysis the rate of pyrophosphorolytic dismutase activity was found to be only moderately slower than the poly-merization activity. These results may help explain the GC-richness of immunoglobulin gene segment joins (N regions) and the loss of bases that occur during gene rearrangements in pre-B and pre-T cells.
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Selected References
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- Alt F. W., Baltimore D. Joining of immunoglobulin heavy chain gene segments: implications from a chromosome with evidence of three D-JH fusions. Proc Natl Acad Sci U S A. 1982 Jul;79(13):4118–4122. doi: 10.1073/pnas.79.13.4118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson R. S., Lawrence C. B., Wilson S. H., Beattie K. L. Genetic relatedness of human DNA polymerase beta and terminal deoxynucleotidyltransferase. Gene. 1987;60(2-3):163–173. doi: 10.1016/0378-1119(87)90224-1. [DOI] [PubMed] [Google Scholar]
- Baltimore D. Is terminal deoxynucleotidyl transferase a somatic mutagen in lymphocytes? Nature. 1974 Mar 29;248(447):409–411. doi: 10.1038/248409a0. [DOI] [PubMed] [Google Scholar]
- Bjursell G., Skoog L. Control of nucleotide pools in mammalian cells. Antibiot Chemother (1971) 1980;28:78–85. doi: 10.1159/000386063. [DOI] [PubMed] [Google Scholar]
- Blackwell T. K., Alt F. W. Molecular characterization of the lymphoid V(D)J recombination activity. J Biol Chem. 1989 Jun 25;264(18):10327–10330. [PubMed] [Google Scholar]
- Chang L. M., Bollum F. J. Doxynucleotide-polymerizing enzymes of calf thymus gland. IV. Inhibition of terminal deoxynucleotidyl transferase by metal ligands. Proc Natl Acad Sci U S A. 1970 Apr;65(4):1041–1048. doi: 10.1073/pnas.65.4.1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang L. M., Bollum F. J. Multiple roles of divalent cation in the terminal deoxynucleotidyltransferase reaction. J Biol Chem. 1990 Oct 15;265(29):17436–17440. [PubMed] [Google Scholar]
- Chang L. M. Development of terminal deoxynucleotidyl transferase activity in embryonic calf thymus gland. Biochem Biophys Res Commun. 1971 Jul 2;44(1):124–131. doi: 10.1016/s0006-291x(71)80167-5. [DOI] [PubMed] [Google Scholar]
- Deibel M. R., Jr, Coleman M. S. Biochemical properties of purified human terminal deoxynucleotidyltransferase. J Biol Chem. 1980 May 10;255(9):4206–4212. [PubMed] [Google Scholar]
- Deutscher M. P., Kornberg A. Enzymatic synthesis of deoxyribonucleic acid. 28. The pyrophosphate exchange and pyrophosphorolysis reactions of deoxyribonucleic acid polymerase. J Biol Chem. 1969 Jun 10;244(11):3019–3028. [PubMed] [Google Scholar]
- Kato K. I., Gonçalves J. M., Houts G. E., Bollum F. J. Deoxynucleotide-polymerizing enzymes of calf thymus gland. II. Properties of the terminal deoxynucleotidyltransferase. J Biol Chem. 1967 Jun 10;242(11):2780–2789. [PubMed] [Google Scholar]
- Komori T., Okada A., Stewart V., Alt F. W. Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes. Science. 1993 Aug 27;261(5125):1171–1175. doi: 10.1126/science.8356451. [DOI] [PubMed] [Google Scholar]
- Kukko-Kalske E., Heinonen J. Inorganic pyrophosphate and inorganic pyrophosphatase in Escherichia coli. Int J Biochem. 1985;17(5):575–580. doi: 10.1016/0020-711x(85)90288-5. [DOI] [PubMed] [Google Scholar]
- Kung P. C., Siverstone A. E., McCaffrey R. P., Baltimore D. Murine terminal deoxynucleotidyl transferase: cellular distribution and response to cortisone. J Exp Med. 1975 Apr 1;141(4):855–865. [PMC free article] [PubMed] [Google Scholar]
- Kunkel T. A., Gopinathan K. P., Dube D. K., Snow E. T., Loeb L. A. Rearrangements of DNA mediated by terminal transferase. Proc Natl Acad Sci U S A. 1986 Mar;83(6):1867–1871. doi: 10.1073/pnas.83.6.1867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lieber M. R. Site-specific recombination in the immune system. FASEB J. 1991 Nov;5(14):2934–2944. doi: 10.1096/fasebj.5.14.1752360. [DOI] [PubMed] [Google Scholar]
- Matsukage A., Nishikawa K., Ooi T., Seto Y., Yamaguchi M. Homology between mammalian DNA polymerase beta and terminal deoxynucleotidyltransferase. J Biol Chem. 1987 Jul 5;262(19):8960–8962. [PubMed] [Google Scholar]
- O'Brien W. E. A continuous spectrophotometric assay for argininosuccinate synthetase based on pyrophosphate formation. Anal Biochem. 1976 Dec;76(2):423–430. doi: 10.1016/0003-2697(76)90337-7. [DOI] [PubMed] [Google Scholar]
- Peterson G. L. Determination of total protein. Methods Enzymol. 1983;91:95–119. doi: 10.1016/s0076-6879(83)91014-5. [DOI] [PubMed] [Google Scholar]
- Robbins D. J., Deibel M. R., Jr, Barkley M. D. Tryptophan fluorescence of terminal deoxynucleotidyl transferase: effects of quenchers on time-resolved emission spectra. Biochemistry. 1985 Dec 3;24(25):7250–7257. doi: 10.1021/bi00346a034. [DOI] [PubMed] [Google Scholar]
- Srivastava A., Modak M. J. Biochemistry of terminal deoxynucleotidyltransferase: identification, characterization, requirements, and active-site involvement in the catalysis of associated pyrophosphate exchange and pyrophosphorolytic activity. Biochemistry. 1980 Jul 8;19(14):3270–3275. doi: 10.1021/bi00555a026. [DOI] [PubMed] [Google Scholar]
- Yancopoulos G. D., Blackwell T. K., Suh H., Hood L., Alt F. W. Introduced T cell receptor variable region gene segments recombine in pre-B cells: evidence that B and T cells use a common recombinase. Cell. 1986 Jan 31;44(2):251–259. doi: 10.1016/0092-8674(86)90759-2. [DOI] [PubMed] [Google Scholar]
