Changes in the activities of DNA polymerases in growing rat lungs

References

• Gutcher G R, Perelman R H. Therapy of hyaline membrane disease. Lung Development: Biological and Clinical Perspectives Neonatal Respiratory Distress, P M Farrell. Academic Press, New York 1982; Vol. II: 107–33
   Google Scholar
• Halliwell B, Aruoma O I. DNA damage by oxygen-derived species. Its mechanism and measurement in mammalian system. FEBS Letter 1991; 281: 9–19
   PubMed Web of Science ®Google Scholar
• Weissbach A. Vertebrate DNA polymerases. Cell 1975; 5: 101–8
   Google Scholar
• Weisbach A, Baltimore D, Bollum F, Gallo R, Korn D. Nomenclature of eukaryotic DNA polymerase. Eur J Biochem 1975; 59: 1–2
   Google Scholar
• Romberg A. DNA replication. W. H. Freeman and Company, San Francisco 1980; 201–25
   Google Scholar
• Bolden A, Noy G P, Weissbach A. DNA polymerase of mitochondria is a 7-polymerase. J Biol Chem 1977; 252: 3351–6
   PubMed Web of Science ®Google Scholar
• Zhang S J, Lee M YWT. Biochemical characterization and development of DNA polymerase α and in the neonatal rat heart. Arch Biochem Biophys 1987; 252: 24–31
   Google Scholar
• Syvaoja J, Suomensaari S, Nishida C, et al. DNA polymerase α, and three distinct enzymes from HeLa cells. Proc Natl Acad Sci USA 1990; 87: 6664–8
   PubMed Web of Science ®Google Scholar
• Kozu T, Seno T, Yagura T. Activity levels of mouse DNA polymerase α-primase complex (DNA replicase) and DNA polymerase α, free from pri-mase activity in synchronized cells, and a comparison of their catalytic properties. Eur J Biochem 1986; 157: 251–9
   Google Scholar
• Hubscher U. The mammalian primase is part of high molecular weight DNA polymerase-α polypeptide. EMBO J 1983; 2: 133–6
   Google Scholar
• Wong S W, Wahl A F, Yuan P-M, et al. Human DNA polymerase α gene expression is cell proliferation dependent and its primary structure is similar to both prokaryotic and eukaryotic replicative DNA polymerases. EMBO J. 1988; 7: 37–47
   PubMed Web of Science ®Google Scholar
• Ikegami S, Taguchi T, Ohashi M, Oguro M, Nagano H, Mano Y. Aphidicolin prevents mitotic cell division by interfering with the activity of DNA polymerase-Q. Nature 1978; 275: 458–60
   PubMed Web of Science ®Google Scholar
• Mille M R, Ulrich R G, Wang T. S-F, Korn D. Monoclonal antibodies against human DNA polymerases inhibit DNA replication in permeabilized human cells. J Biol Chem 1985; 260: 134–8
   Google Scholar
• So A G, Downey K M. Mammalian DNA polymerase α and current status in DNA replication. Biochemistry 1988; 27: 4591–5
   PubMedGoogle Scholar
• Pacifici R E, Davies K JA. Protein, lipid and DNA repair systems in oxidative stress: the free-radical theory of aging revisited. Gerontology 1991; 37: 166–80
   PubMed Web of Science ®Google Scholar
• Ohashi M, Taguchi T, Ikegami S. Aphidicolin; a specific inhibitor of DNA polymerases in the cyto-sol of rat liver. Biochem Biophys Res Commun 1978; 82: 1084–90
   PubMed Web of Science ®Google Scholar
• Katsura H, Taguchi T, Kida K. Alterations in DNA synthesis and cellular constituents in mouse lung following bleomycin injections. Am J Respir Cell Mol Biol 1992; 6: 190–6
   PubMed Web of Science ®Google Scholar
• Wagar M A, Evans M J, Huberman J A. Effect of 2′3′-dideoxythmidine-5′-triphosphate on Hela cell in vitro DNA synthesis: evidence that DNA polymerase α is the only polymerase required for cellular DNA replication. Nucleic Acids Res 1978; 5: 1933–46
   Google Scholar
• Burton K. A study of the conditions and mechanism of the diphenylamine reaction for the calori-metric estimation of deoxyribo-nucleic acid. Biochem J 1956; 62: 315–9
   PubMed Web of Science ®Google Scholar
• Hochberg Y, Tamhane A C. Multiple comparison procedures. John Wiley & Sons, New York 1987
   Google Scholar
• Burri P H. The postnatal growth of the rat lung. III. Morphology. Anat Rec 1974; 180: 77–98
   PubMedGoogle Scholar
• Kauffman S L, Burri P H, Weibel E R. The postnatal growth of the rat lung. II. Autoradiography. Anat Rec 1974; 180: 63–76
   PubMedGoogle Scholar
• Burri P H, Dbaly J, Weibel E R. The postnatal growth of the rat lung. I. Morphometry. Anat Rec 1974; 178: 711–30
   PubMedGoogle Scholar
• Bucher J R, Robert R J. The development of the newborn rat lung in hyperoxia: a dose-response study of lung growth, maturation, and changes in antioxidant enzyme activities. Pediatr Res 1981; 15: 999–1008
   PubMed Web of Science ®Google Scholar
• Kuboi S, Mizuuchi A, Mizuuchi T, Taguchi T, Thurlbeck W M, Kida K. DNA synthesis and related enzymes altered in compensatory lung growth in rats. 1992; Scand J Clin Lab Invest 1992; 52: 707–15
   PubMed Web of Science ®Google Scholar
• Riley D J, Rannels D E, Low R B, Jensen L, Jacobs T P. NHLBI workshop summary. Effect of physical forces on lung structure, function, and metabolism. Am Rev Respir Dis 1990; 142: 910–4
   PubMed Web of Science ®Google Scholar
• Rao K VS, Rao K S. Increased DNA polymerase β-activity in different regions of aging rat brain. Biochem Intern 1984; 9: 391–7
   Google Scholar
• Shrivastaw K P, Philippe M, Chevaillier P. DNA-polymerases in neuron and glial cells of developing and aging mouse brain. J Neurosci Res 1983; 9: 1–10
   Google Scholar
• Hubscher U, Kuenzle C C, Limacher W, Scherrer P, Spadari S. Functions of DNA polymerases α, β, and γ in neurons during development. Cold Spring Harb Symp Quant Biol 1978; 43: 625–9
   Google Scholar
• Hubscher U, Kuenzle C C, Spadari S. Variation of DNA polymerases-α, -β, and -γ during perinatal tissue growth and differentation. Nucleic Acids Res 1977; 4: 2917–29
   PubMedGoogle Scholar
• Limas C J, Limas C. DNA polymerases during postnatal myocardial development. Nature 1978; 271: 781–3
   PubMedGoogle Scholar
• Matsukage A, Kitani H, Yamaguchi M, Kusakabe M, Morita T, Koshida Y. Differentiation of lens and neural cells in chicken embryo is accompanied by simultaneous decay of DNA replication machinery. Devel Biol 1986; 117: 226–32
   PubMed Web of Science ®Google Scholar