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Deregulation of DNA polymerase β by sense and antisense RNA expression in mouse 3T3 cells alters cell growth

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Somatic Cell and Molecular Genetics

Abstract

DNA polymerase beta (β-pol) and its mRNA are maintained at constitutive levels during the cell cycle and during stages of cell growth in culture. To study biological consequences of variations in the level of this DNA repair enzyme and/or its mRNA, we prepared expression vectors in which cDNA for human β-pol is inserted under the control of a metallothionein promoter (pMT) in the sense and antisense orientation, respectively, and these vectors then were used for stable transformation of mouse 3T3 cells. Vectors also contained the mouseDHFR gene, such that culture of transformants in medium with increasing concentrations of methotrexate resulted in amplification of inserted DNA. The levels of sense and antisense transcripts are strongly increased by culture of transformants in medium with 65 µM Zn2+, although some expression is detected even without Zn2+ induction. After five days of induction, the β-pol level was about threefold higher in sense cells and about 10-fold lower in antisense cells than in parallel cultures without induction. The antisense line has a threefold increased cell doubling time in the presence of 65 µM Zn2+ compared with the absence of Zn2+. Zn2+ (65 µM) induction for the sense line results in normal growth for the first three days and, thereafter, a complete cessation of growth. Yet, these blocked cells remain fully viable. The results indicate that sudden deregulation of β-pol expression alters cell growth in mouse 3T3 cells.

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Literature cited

  1. Blake, K.R., Murakami, A., and Miller, P.S. (1985).Biochemistry 246132–6138.

    Google Scholar 

  2. Melton, D.A. (1985).Proc. Natl. Acad. Sci. U.S.A. 82144–148.

    Google Scholar 

  3. Green, P.J., Pines, O., and Inouye, M. (1986).Annu. Rev. Biochem. 55569–597.

    Google Scholar 

  4. Inouye, M. (1988).Gene 7225–34.

    Google Scholar 

  5. Knecht, D.A., and Loomis, W.F. (1987).Science 2361081–1086.

    Google Scholar 

  6. Teichman-Weinberg, A., Littauer, U.Z., and Ginzburg, I. (1988).Gene 72297–307.

    Google Scholar 

  7. Giebelhaus, D.H., Eib, D.W., and Moon, R.T. (1988).Cell 53601–615.

    Google Scholar 

  8. Rodermel, S.R., Abbott, M.S., and Bogorad, L. (1988).Cell 55673–681.

    Google Scholar 

  9. Wilson, S.H. (1990). InThe Eukaryotic Nucleus, Vol I (eds.) Strauss, P., and Wilson, S. (The Telford Press, Caldwell, New Jersey), pp. 199–234.

    Google Scholar 

  10. SenGupta, D.N., Zmudzka, B.Z., Kumar, P., Cobianchi, F., Skowronski, J., and Wilson, S.H. (1986).Biochem. Biophys. Res. Commun. 136341–347.

    Google Scholar 

  11. Graham, F.L., and van der Eb, A. (1973).Virology 52456–467.

    Google Scholar 

  12. McBride, O.W., Zmudzka, B.Z., and Wilson, S.H. (1987).Proc. Natl. Acad. Sci. U.S.A. 84503–507.

    Google Scholar 

  13. Maniatis, T., Fritsch, E.F., and Sambrook, T. (1982).Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Laboratory, Cold Spring Harbor, New York).

    Google Scholar 

  14. DeLeon, D.V., Cox, K.H., Angerer, L.M., and Angerer, R. (1983).Dev. Biol. 100197–206.

    Google Scholar 

  15. Karawya, E., Swack, J., and Wilson, S.H. (1983).Anal. Biochem. 135318–325.

    Google Scholar 

  16. Abbotts, J., SenGupta, D.N., Zmudzka, B., Widen, S., Notario, V., and Wilson, S.H. (1988).Biochemistry 27901–909.

    Google Scholar 

  17. Choo, K.H., Filby, R.G., Yennings, J.G., Peterson, G., and Fowler, K. (1986).DNA 5529–537.

    Google Scholar 

  18. Okayama, H., and Berg, P. (1983).Mol. Cell Biol. 3280–289.

    Google Scholar 

  19. Rein, D., Recupero, A.J., Reed, M.P., and Meyer, R.R. (1990). InThe Eukaryotic Nucleus, Vol. I (eds.) Strauss, P., and Wilson, S. (The Telford Press, Caldwell, New Jersey), pp. 95–123.

    Google Scholar 

  20. Kumar, A., Widen, S.G., Williams, K.R., Kedar, P., Karpel, R.L., and Wilson, S.H. (1990).J. Biol. Chem. 2652124–2131.

    Google Scholar 

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Zmudzka, B.Z., Wilson, S.H. Deregulation of DNA polymerase β by sense and antisense RNA expression in mouse 3T3 cells alters cell growth. Somat Cell Mol Genet 16, 311–320 (1990). https://doi.org/10.1007/BF01232459

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  • DOI: https://doi.org/10.1007/BF01232459

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