Abstract
During early morphogenesis, organ- or tissue-specific “stem” cell lines are established. Initially multipotent, the progeny become committed to the expression of an increasingly restricted number of specialized phenotypes. The process leading to acquisition by cells of specialized structures and/or functions is called cell differentiation. Implicit in such a process is the progressive loss of the potential for tissue metaplasia, i.e., the ability to be reprogramed and converted into another phenotype. A rare exception to this rule in vertebrates is the Wolffian lens regeneration in lentectomized newts where fully differentiated melanocytes from the dorsal iris dedifferentiate, proliferate and then redifferentiate into lens fiber cells (Yamada 1977).
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References
Appleby D.W., Modak S.P.: DNA degradation in terminally differentiating lens fiber cells from chick embryos. Proc. Natl. Acad. Sci. USA 74, 5579–5583 (1977).
Axel R.: Cleavage of DNA in nuclei and chromatin with staphylococcal nuclease. Biochemistry 14, 2921–2925 (1975).
Axel R., Cedar H., Felsenfeld G.: Synthesis of globin ribonucleic acid from duck-reticulocyte chromatin in vitro. Proc. Natl. Acad. Sci. USA 70, 2029–2032 (1973).
Barton R.W., Yang W.K.: Low molecular weight DNA polymerase decreased activity in spleens of old Balb/c mice. Mech. Ageing Dev. 4, 123–136 (1975).
Bodell W.J.: Non-uniform distribution of DNA repair in chromatin after treatment with methyl methanesulfonate. Nucleic Acids Res. 4, 2619–2628 (1977).
Bradbury E.M.: Histone interactions and chromatin structure. In: The organization and expression of eukaryotic genome (eds. E.M. Bradbury, K. Javaherian), pp. 99–123. New York-London: Academic Press 1977.
Brash D.E., Hart R.W.: DNA damage and repair in vivo. J. Environmental Pathol. Toxicol. 2, 79–114 (1978).
Chan A.C., Ng S.K.C., Walker I.G.: Reduced DNA repair during differentiation of a myogenic cell line. J. Cell Biol. 70, 685–691 (1976).
Clark R.J., Felsenfeld G.: Structure of chromatin. Nature New Biol. 229, 101–106 (1971).
Clark R.J., Felsenfeld G.: Association of arginine-rich histones with GC-rich regions of DNA. Nature New Biol. 240, 226–229 (1972).
Cleaver J.E.: Nucleosome structure controls rates of excision repair in DNA of human cells. Nature (London) 270, 451–453 (1977).
Compton J.L., Hancock R., Oudet P., Chambon P.: Biochemical and electron microscopic evidence that the subunit structure of chinese-hamster-ovary interphase chromatin is conserved in mitotic chromosomes. Eur. J. Biochem. 70, 555–568 (1975).
Counis M.-F., Chadun E., Courtois Y.: DNA snythesis and repair in terminally differentiating embryonic lens cells. Dev. Biol. 57, 47–55 (1977).
D’Ambrosio S.M., Setlow R.B.: On the presence of UV-endonuclease sensitive site in mammalian DNA. In: DNA repair mechanisms (eds. P.C. Hanawelt, E. Freidberg, C.F. Fox), Vol. IX, pp. 499–503. New York: Academic Press 1978.
Garel A., Axel R.: Selective digestion of transcriptionally active ovalbumin genes from oviduct nuclei. Proc. Natl. Acad. Sci. USA 73, 3966–3970 (1973).
Garrard W.D., Bonner J.: Changes in chromatin proteins during liver regeneration. J. Biol. Chem. 249, 3729–3736 (1974).
Gilmour R.S., Paul J.: Tissue-specific transcription of the globin gene in isolated chromatin. Proc. Natl. Acad. Sci. USA 70, 3440–3442 (1973).
Goldstein S.: The biology of aging. New Engl. J. Med. 285, 1120–1129 (1971).
Goth R., Rajewsky M.F.: Persistence of 06-ethylguanine in rat brain DNA: correlation with nervous system-specific carcinogenesis by ethylnitrosourea. Proc. Natl. Acad. Sci. USA 71, 639–643 (1974).
Hahn F.M., King D., Yang S.J.: Quantitative changes in unscheduled DNA synthesis in rat muscle cells after differentiation. Nature New Biol. 230, 242–244 (1971).
Hart R.W., Setlow R.B.: Correlation between deoxyribonucleic acid excision repair and life-span in a number of mammalian species. Proc. Natl. Acad. Sci. USA 71, 2169–2173 (1974).
Hart R.W., Setlow R.B.: DNA repair in late-passage human cells. Mech. Ageing Dev. 5, 67–7 (1976).
Hart R.W., D’Ambrosio S.M., Ng K.K., Modak S.P.: Longevity, stability and DNA repair. Mech. Ageing Dev. 9, 203–223 (1979).
Hewish D.R., Burgoyne L.A.: Chromatin sub-structure. The digestion of chromatin DNA at regularly spaced sites by a nuclear deoxyribonuclease. Biochem. Biophys. Res. Commun. 52, 504–510 (1973).
Kakunaga R.: The role of cell division in the malignant transformation of mouse cells treated with 3-methylcholanthrene. Cancer Res. 35, 1637–1642 (1975).
Kakunaga T.: Requirement for cell replication in the fixation and expression of the transformed state in mouse cells treated with 4-nitroquinolin-1-oxide. Int. J. Cancer 14, 736–742 (1974).
Karran P., Ormerod M.G.: Is the ability to repair damage to DNA related to the proliferative capacity of a cell? The rejoining of X-ray produced strand breaks. Biochim. Biophys. Acta 299, 54–64 (1973).
Karran P., Moscona A., Strauss B.: Developmental decline in DNA repair in neural retina cells of chick embryos. J. Cell Biol. 74, 274–286 (1977).
Koostra A., Slaga T.J., Olins D.E.: Binding of Benzo(A) pyrene diol epoxide to chromatin. Biophys. J. 21, 67a (1978).
Kornberg R.D.: Chromatin structure: A repeating unit of histones and DNA. Science 184, 868–871 (1974).
Kornberg R.D., Thomas J.O.: Chromatin structure oligomers of the histones. Science 184, 865–868 (1974).
Linn S., Kairis M., Holliday R.: Decreased fidelity of DNA polymerase activity isolated from aging human fibroblasts. Proc. Natl. Acad. Sci. USA 73, 2818–2822 (1976).
Little J.B.: Relationship between DNA repair capacity and cellular aging. Gerontology 22, 28–55 (1976).
Lohr D., Corden J., Tatchell K., Kovacic R.T., van Holde K.E.: Comparative subunit structure of HeLa, yeast and chicken erythrocyte chromatin. Proc. Natl. Acad. Sci. USA 74, 79–83 (1977).
Maher V.M., McCormick J.J.: Effect of DNA repair on the cytotoxicity and mutagenesis of UV radiation and chemical carcinogens in normal and Xeroderma pigmentosum cells. In: Biology of Radiation Carcinogenesis (eds. J.M. Yuhas, R.W. Tennant, J. Regan), pp. 129–145. New York: Raven Press 1976.
Maher V.M., Quellette L.M., Curren R.D., McCormick J.J.: Frequency of UV-light-induced mutation is higher in Xeroderma Pigmentosum variant cells than in normal cells. Nature (London) 261, 593–595 (1976).
Massie H.R., Baird M.B., Nicolosi R.J.: Changes in the structure of rat liver DNA in relation to age. Arch. Biochem. Biophys. 153, 736–741 (1972).
Mattern M.R., Cerutti P.A.: Selective excision of gammay ray damaged thymine from the DNA of cultured mammalian cells. Biochim. Biophys. Acta 395, 48–55 (1975).
Milo G.E., Hart R.W.: Age-related alterations in plasma membrane glycoprotein content and scheduled or unscheduled DNA synthesis. Arch. Biochem. Biophys. 176, 324–333 (1976).
Modak S.P.: A model for transcriptional control in terminally differentiating lens fiber cells. In: Cell Differentiation (eds. R. Harris, P. Allin, D. Viza), pp. 339–342. Copenhagen: Munksgaard 1972.
Modak S.P.: Two-dimensional electrophoresis of native and denatured DNA from chromatin digests. Experienta 34, 57 (1978).
Modak S.P., Bollum F.J.: Terminal lens cell differentiation. III. Initiator activity of DNA during nuclear degeneration. Exp. Cell Res. 62, 421–432 (1970).
Modak S.P., Bollum F.J.: Detection and measurement of single-strand breaks in nuclear DNA in fixed lens sections. Exp. Cell Res. 75, 307–313 (1972).
Modak S.P., Perdue S.W.: Terminal lens cell differentiation. I. Histological and microspectrophotometric analyses of nuclear degeneration. Exp. Cell Res. 59, 43–56 (1970).
Modak S.P., Price G.B.: Exogenous DNA polymerase-catalyzed incorporation of deoxyribonucleotide monophosphates in nuclei of fixed mouse brain cells: Changes associated with age and X-irradiation. Exp. Cell Res. 65, 289–298 (1971).
Modak S.P., Traurig H.: Appearance of strand breaks in the nuclear DNA of terminally differentiating vaginal epithelium. Cell Differ. 2, 351–355 (1972).
Modak S.P., von Borstel R.C., Bollum F.J.: Terminal lens cells differentiation. II. Template activity of DNA during nuclear degeneration. Exp. Cell Res. 56, 105–113 (1969).
Modak S.P., Appleby D.W., Chappuis M.: Cytoplasmic informational DNA: Fact or Fantasy? J. Cell Biol. 70, 140a (1976).
Modak S.P., Gonet C., Unger-Ullmann C., Chappuis M.: Chromatin structure in aging mouse liver. Experienta 34, 57 (1978).
Morris N.R.: A comparison of the structure of chick erythrocyte and chick liver chromatin. Cell 9, 627–632 (1976).
Noll M.: Subunit structure of chromatin. Nature (London) 251, 249–251 (1974).
Olins A.L., Olins D.E.: Spheroid chromatin units (v Bodies). Science 183, 330–332 (1974).
Peleg L., Raz E., Ben-Ishai R.: Changing capacity for DNA excision-repair in mouse embryonic cells in vitro. Exp. Cell Res. 104, 301–307 (1977).
Piatigorsky J., Rothschild S.S., Milstone L.M.: Differentiation of lens fibers in explanted embryonic chick lens epithelia. Dev. Biol. 34, 334–345 (1973).
Price G.B., Modak S.P., Makinodan T.: Age-associated changes in the DNA of mouse tissue. Science 171, 917–920 (1971).
Radman M.: SOS repair hypothesis: Phenomenology of an inducible DNA repair which is accompanied by mutagenesis. In: Molecular Mechanisms for Repair of DNA (eds. P.C. Hanawalt, R.B. Setlow), pp. 355–368. New York: Plenum Press 1975.
Ruiz-Carrillo A., Wangh L.J., Allfrey V.G.: Processing of newly snythesized histone molecules. Science 190, 117–128 (1975).
Sacher G.A., Hart R.W.: Longevity, aging and comparative cellular and molecular biology of the house mouse Mus musculus and the white footed mouse, Peromyscus leucopus. In: Birth Defects—Original Article Ser. 14, 71–98 (1978).
Shaw B.R., Herman T.M., Kovacic R.T., Beaudreau G.S., van Holde K.E.: Analysis of subunit organization in chicken erythrocyte chromatin. Proc. Natl. Acad. Sci. USA 73, 505–509 (1976).
Skalka M., Matyasova J., Cejkova M.: DNA in chromatin of irradiated lymphoid tissues degraded in vivo into regular fragments. FEBS Lett. 72, 271–274 (1976).
Sollner-Webb B., Felsenfeld G.: A comparison of the digestion of nuclei and chromatin by staphylococcal nuclease. Biochemistry 14, 2915–2920 (1975).
Smith-Sonneborn J.: DNA repair and longevity assurance in Paramecium tetraurelia. Science 203, 1115–1117 (1978).
Stockdale F.E.: Changing levels of DNA polymerase activity during the development of skeletal muscle tissue in vivo. Dev. Biol. 21, 462–474 (1970).
Stockdale F.E.: DNA synthesis in differentiating skeletal muscle cells: initiation by ultraviolet light. Science 171, 1145–1147 (1971).
Stockdale F.E., O’Neill M.C.: Repair DNA synthesis in differentiated embryonic muscle cells. J. Cell Biol. 52, 589–597 (1972).
Thomas J.O.: Aspects of the structure of chromatin. In: The Organization and expression of eukaryotic genome (eds. E.M. Bradbury, K. Javaherian), pp. 83–98. New York-London: Academic Press 1977.
Todd R.D., Garrard W.T.: Two-dimensional electrophoretic analysis of polynucleosomes. J. Biol. Chem. 252, 4729–4738 (1977).
Tréton, J., Modak, S.P., Courtois, Y.: Analysis of thimidine incorporation in the DNA of chick embryo lens epithelium and lens fibers irradiated with ultraviolet light. Exp. Eye Res., in press (1980).
Unger-Ullmann C., Modak S.P.: Gel electrophoretic analysis of histones in late chick embryo lens epithelium, lens fiber, liver, brain and erythrocyte. Differentiation 12, 135–144 (1979).
Varshavsky A.J., Bakayev V.V., Gerogiev G.P.: Heterogeneity of chromatin subunits in vitro and location of histone H1. Nucleic Acids Res. 3, 477–492 (1976).
Weintraub H.: The nucleosome repeat length increases during erythropoiesis in the chick. Nucleic Acid Res. 5, 1179–1188 (1978).
Weintraub H., Groudine M.: Chromosomal subunits in active genes have an altered conformation. Science 193, 848–856 (1976).
Weintraub H., Worcel A., Alberts B.: A model for chromatin based upon two symmetrically paired half-nucleosomes. Cell 9, 409–417 (1976).
Wheeler K.T., Lett J.T.: On the possibility that DNA repair is related to age in nondividing cells. Proc. Natl. Acad. Sci. USA 71, 1862–1865 (1974).
Whitlock J.P., Simpson R.T.: Removal of histone H1 exposes a fifty base pair DNA segment between nucleosomes. Biochemistry 15, 3307–3314 (1976).
Wilkins R.J., Hart R.W.: Preferential DNA repair in human cells. Nature New Biol. 247, 35–36 (1973).
Witkin E.M.: Ultraviolet-induced mutation and inducible DNA repair in Escherichia coli. Bacteriol. Rev. 40, 869–907 (1976).
Witkin E.M., George D.L.: Ultraviolet mutagenesis in Pol A and Uvr A Pol h derivatives of Escherichia coli B/R: Evidence for an inducible error-prone repair system. Genetics 73 (Suppl), 91–108 (1973).
Yamada T.: Control mechanisms in cell-type conversion in Newt lens regeneration. In: Monographs in Developmental Biology, Vol. XIII (ed. A. Wolsky), pp. 1–126. Basel: Karger 1977.
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Modak, S.P., Unger-Ullmann, C. (1980). Control of Genome Integrity in Terminally Differentiating and Postmitotic Aging Cells. In: McKinnell, R.G., DiBerardino, M.A., Blumenfeld, M., Bergad, R.D. (eds) Differentiation and Neoplasia. Results and Problems in Cell Differentiation, vol 11. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-38267-6_23
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DOI: https://doi.org/10.1007/978-3-540-38267-6_23
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