Skip to main content
Log in

The evolutionary transition from RNA to DNA in early cells

  • Published:
Journal of Molecular Evolution Aims and scope Submit manuscript

Summary

The evolution of genetic material can be divided into at least three major phases: first, genomes of “nucleic acid-like” molecules; secondly, genomes of RNA; and finally, double-stranded DNA genomes such as those present in all contemporary cells. Using properties of nucleic acid molecules, we attempt to explain the evolutionary transition from RNA alone as a cellular informational macromolecule prior to the evolution of cell systems based on double-stranded DNA. The idea that ribonucleic acid-based cellular genomes preceded DNA is based on the following: (1) protein synthesis can occur in the absence of DNA but not of RNA; (2) RNA molecules have some catalytic properties; (3) the ubiquity of purine and pyridine nucleotide coenzymes as well as other similar ribonucleotide cofactors in metabolic pathways; and (4) the fact that the biosynthesis of deoxyribonucleotides always proceeds via the enzymatic reduction of ribonucleotides.

The “RNA prior to DNA” hypothesis can be further developed by understanding the selective pressures that led to the biosynthesis of deoxyribose, thymine, and proofreading DNA polymerases. Taken together these observations suggest to us that DNA was selected as an informational molecule in cells to stabilize earlier RNA-protein replicating systems. These arguments include the facts that (1) the 2′-deoxy-containing phosphodiester backbone is more stable in aqueous conditions and in the presence of transition metal ions (such as Zn2+) than its ribo-equivalents; (2) the absence of proofreading activity in RNA polymerases leads to a higher rate of mutation in RNA genomes relative to DNA; (3) information in RNA degrades because of the tendency of cytosine to deaminate to uracil and the lack of a correcting enzyme; and (4) UV irradiation produces a larger number of photochemical changes in RNA molecules relative to double-stranded DNA. The absence of atmospheric UV attenuation during the early Earth environment (Hadean and early Archean) would have imposed an intense selection pressure favoring duplex DNA over other genetic information storage systems.

If RNA preceded DNA as a reservior of cellular genetic information, then an RNA-replicating oligopeptide must have been one of the earliest protoenzymes from which RNA polymerase presumably evolved. We conclude that RNA polymerases are among the oldest classes of enzymes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literatur

  • Adman R, Grossman L (1965) Action of the RNA polymerase on UV-irradiated poly(U). Fed Proc 24:602

    Google Scholar 

  • Adman R, Grossman L (1967) Template properties of polyribonucleotides containing uracil or modified uracil in the RNA polymerase reaction. J Mol Biol 23:417–439

    PubMed  Google Scholar 

  • Awramik SM, Schopf JW, Walter MR (1983) Filamentous bacteria from the Archean of western Australia. Precambrian Res 20:357–374

    Google Scholar 

  • Baltscheffsky H, Alauddin M, Falk G, Lundin M (1987)_Similarities between soluble inorganic pyrophosphatase from yeast and some nucleotide-binding polypeptides. Acta Chem Scand B 41:106–107

    PubMed  Google Scholar 

  • Bertani LE, Häggmark A, Reichard P (1963) Enzymatic synthesis of deoxyribonucleotides. II. Formation and interconversion of deoxyuridine phosphates. J Biol Chem 238:3407–3413

    PubMed  Google Scholar 

  • Bridson PK, Fakhrai H, Lornmann R, Orgel LE, van Roode M (1981) Template-directed synthesis of oligoguanylic acids-metal ions catalysis. In: Wolman Y (ed) Origins of life. Reidel, Dordrecht, pp 233–239

    Google Scholar 

  • Butzow JJ, Eichhorn GL (1965) Interaction of metal ions with nucleic acids and related compounds. V. The relative effect of transition metals. Biopolymers 3:95–103

    PubMed  Google Scholar 

  • Butzow JJ, Eichhorn GL (1971) Interaction of metal ions with nucleic acids and related compounds. XVII. On the mechanism of degradation of polyribonucleotides by zinc (II) ions. Biochemistry 10:2019–2027

    PubMed  Google Scholar 

  • Cantó J, Mendoza E (eds) (1983) Memorias del symposio sobre objetos Herbig-Haro. Rev Mex Astron Astrofis, vol 7

  • Cantor CR, Schimmel PR (1980) Biophysical chemistry. WH Freeman, San Francisco

    Google Scholar 

  • Canuto VM, Levine JS, Augustssen TR, Imhoff CL (1982) UV radiation from the young sun and levels of of O2 and O3 in the prebiological paleoatmosphere. Nature 296:816–820

    Google Scholar 

  • Canuto VM, Levine JS, Augustssen TR, Imhoff CL (1983) Oxygen and ozone in the early Earth's atmosphere. Precambrian Res 20:109–120

    Google Scholar 

  • Cerutti P, Ikeda K, Witkop B (1965) The selective photoreduction of uridine in polynucleotides. J Am Chem Soc 87:2505–2507

    PubMed  Google Scholar 

  • Crick FHC (1968) The origin of the genetic code. J Mol Biol 38:367–379

    PubMed  Google Scholar 

  • Darnell JE, Doolittle WF (1986) Speculations on the early course of evolution. Proc Natl Acad Sci USA 83:1271–1275

    PubMed  Google Scholar 

  • Diener TO (1982) Viroids and their interaction with host cells. Annu Rev Microbiol 36:239–258

    PubMed  Google Scholar 

  • Eichhorn GL, Tarien E, Butzow JJ (1971) Interaction of metal ions with nucleic acids and related compounds. XVI. Specific cleavage effects in the depolymerization of ribonucleic acids by zinc (II) ions. Biochemistry 10:2014–2019

    PubMed  Google Scholar 

  • Eigen M, Schuster P (1977) The hypercycle-a principle of natural self-organization. Part A: emergence of the hypercycle. Naturwissenschaften 64:541–565

    PubMed  Google Scholar 

  • Ferris JP, Usher DA (1983) Origins of life. In: Zubay G (ed) Biochemistry. Addison Wesley, Reading MA, pp 1191–1241

    Google Scholar 

  • Fersht AR (1979) Fidelity of replication of phage ϕX 174 DNA by DNA polymerase III holoenzyme: spontaneous mutations by misincorporation. Proc Natl Acad Sci USA 76:4946–4950

    PubMed  Google Scholar 

  • Fersht AR (1983) Enzymic editing mechanisms in protein synthesis and DNA replication. In: Hunt T, Prentis S, Tooze J (eds) DNA makes RNA makes proteins. Elsevier Medical Press, Cambridge, pp 226–232

    Google Scholar 

  • Freidberg EC (1985) DNA repair. WH Freeman, San Francisco

    Google Scholar 

  • Gaustad JE, Vogel SN (1982) High energy solar radiation and the origin of life. Origins of Life 12:3–8

    PubMed  Google Scholar 

  • Grossman L (1963) The effects of ultraviolet-irradiated polyuridylic acid in cell-free protein synthesis inEscherichia coli, II. The influence of specific photoproducts. Proc Natl Acad Sci USA 50:657–664

    PubMed  Google Scholar 

  • Guerrier-Takada C, Gardiner K, Marsh T, Pace N, Altman S (1983) The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme. Cell 35:849–857

    PubMed  Google Scholar 

  • Haldane JBS (1965) Data needed for a blueprint of the first organism. In: Fox SW (ed) The origin of prebiological systems and their molecular matrices. Academic Press, New York, pp 11–15

    Google Scholar 

  • Halmann M, Sanchez RA, Orgel LE (1969) Phosphorylation of D-ribose in aqueous solution. J Org Chem 34:3702–3703

    Google Scholar 

  • Hartman H, Lawless JG, Morrison P (eds) (1985) The search for the universal ancestors. NASA SP-477, Washington DC

  • Holland J, Spindler K, Horodyski F, Graban E, Nichol S, VandePol S (1982) Rapid evolution of RNA genomes. Science 215: 1577–1585

    PubMed  Google Scholar 

  • Joyce GF, Schwartz AW, Miller SL, Orgel LE (1987) The case for an ancestral genetic system involving simple analogues of the nucleotides. Proc Natl Acad Sci USA 84:4398–4402

    PubMed  Google Scholar 

  • Kamer G, Argos P (1984) Primary structural comparison of RNA-dependent polymerases from plant, animal and bacterial viruses. Nucleic Acids Res 12(18):7269–7282

    PubMed  Google Scholar 

  • Knoll AH, Barghoorn ES (1977) Archean microfossils showing cell division from the Swaziland system of South Africa. Science 198:396–398

    Google Scholar 

  • Kornberg A (1980) DNA replication. WH Freeman, San Francisco

    Google Scholar 

  • Kruger K, Grabowski PJ, Zaug AJ, Sands J, Gottschlin DE, Cech TR (1982) Self-splicing RNA autoexcision and autocyclization of the ribosomal RNA intervening sequence ofTetrahymena. Cell 31:147–157

    PubMed  Google Scholar 

  • Lammers M, Follmann H (1983) The ribonucleotide reductases—a unique group of metalloenzymes essential for cell proliferation. Struct Bonding 54:27–91

    Google Scholar 

  • Lazcano, A (1986) Prebiotic evolution and the origin of cells. Treballs Soc Cat Biol 39:73–103

    Google Scholar 

  • Lazcano A, Oró J, Miller SL (1983) Primitive Earth environments: organic syntheses and the origin and early evolution of life. Precambrian Res 20:259–282

    Google Scholar 

  • Lazcano A, Valverde V, Fastag J, Gariglio P, Ramírez C, Oró J (1987) Molecular evolution of nucleic acid polymerases. In: Eirich F, Ponnamperuma C (eds) Prebiological organization. Proceedings of the VIII College Park Colloquium on Chemical Evolution (in press)

  • Lazcano A, Fastag J, Gariglio P, Ramírez C, Oró J (1988) On the early evolution of RNA polymerase. J Mol Evol (in press)

  • Lindahl T (1982) DNA repair enzymes. Annu Rev Biochem 51:61–87

    PubMed  Google Scholar 

  • Llaca V, Silva E, Lazcano A, Rangel LM, Gariglio P, Oró J (1987) In search of the ancestral RNA polymerase: an experimental approach. In: Eirich F, Ponnamperuma C (eds) Prebiological organization. Proceedings of the VIII College Park Colloquium on Chemical Evolution (in press)

  • Loeb LA, Kunkel TA (1982) Fidelity of DNA synthesis. Annu Rev Biochem 51:429–457

    PubMed  Google Scholar 

  • Mar A, Dworkin J, Oró J (1987) Non-enzymatic synthesis of the coenzymes uridine diphosphate glucose and cytidine diphosphate choline and other phosphorylated metabolic intermediates. Origins of Life and Evolution of the Biosphere (in press)

  • Margulis L (1981) Symbiosis in cell evolution. WH Freeman, San Francisco

    Google Scholar 

  • Margulis L, Guerrero R (1988) From origins of life to evolution of microbial communities: a minimalist approach. In: Eirich F, Ponnamperuma C (eds) Prebiological organization. Proceedings of the VIII College Park Colloquium on Chemical Evolution (in press)

  • Margulis L, Sagan D (1986) The origins of sex. Yale University Press, New Haven

    Google Scholar 

  • Margulis L, Walker JCG, Rambler M (1976) A reassessment of the roles of oxygen and ultraviolet light in Precambrian evolution. Nature 284:620–624

    Google Scholar 

  • McLaren AD, Shugar D (1964) Photochemistry of proteins and nucleic acids. Pergamon, Oxford

    Google Scholar 

  • Mildvan A, Loeb L (1979) The role of metal ions in the mechanisms of DNA and RNA polymerases. CRC Crit Rev Biochem 6:219–244

    PubMed  Google Scholar 

  • Miller SL, Orgel LE (1974) The origins of life on Earth. Prentice-Hall, Englewood Cliffs NJ

    Google Scholar 

  • Olivera BM (1978) DNA intermediates at theEscherichia coli replication fork: effect of dUTP. Proc Natl Acad Sci USA 75: 238–243

    PubMed  Google Scholar 

  • Ono J, Wilson RG, Grossman L (1965) Effects of ultraviolet light on the template properties of polycytidylic acid. J Mol Biol 11:600–612

    PubMed  Google Scholar 

  • Oparin AI (1961) Life: its nature, origin and development. Oliver and Boyd, Edinburgh

    Google Scholar 

  • Orgel LE (1968) Evolution of the genetic apparatus. J Mol Biol 38:380–393

    Google Scholar 

  • Orgel LE, Lohrmann R (1974) Prebiotic chemistry and nucleic acid replication. Acc Chem Res 1:368–377

    Google Scholar 

  • Oró J (1965) Stages and mechanisms of prebiological organic synthesis. In: Fox SW (ed) The origin of prebiological systems and their molecular matrices. Academic Press, New York, pp 137–161

    Google Scholar 

  • Oró J, Lazcano A (1984) A minimal living system and the origin of a protocell. Adv Space Res 4:167–176

    PubMed  Google Scholar 

  • Oró J, Lazcano A (1988) A holistic precellular organization model. In: Eirich F, Ponnamperuma C (eds) Prebiological organization. Proceedings of the VIII College Park Colloquium on Chemical Evolution (in press)

  • Pace N, Marsh T (1985) RNA catalysis and the origin of life. Origins Life 16:97–116

    Google Scholar 

  • Pearson M, Johns HE (1966) Suppression of hydrate and dimer formation in ultraviolet-irradiated poly (A+U) relative to poly (U). J Mol Biol 20:215–229

    PubMed  Google Scholar 

  • Rambler M, Margulis L (1980) Bacterial resistance to UV radiation under anaerobiosis: implications for pre-Phanerozoic evolution. Science 210:638–640

    PubMed  Google Scholar 

  • Raenney DC (1979) RNA splicing and polynucleotide evolution. Nature 227:597–600

    Google Scholar 

  • Reanney DC (1982) The evolution of RNA viruses. Annu Rev Microbiol 36:47–73

    PubMed  Google Scholar 

  • Remsen JF, Cerutti PA (1972) Ultraviolet inactivation and miscoding of irradiated R17-RNA in vitro. Biochem Biophys Res Commun 48:430–436

    PubMed  Google Scholar 

  • Rich A (1962) On the problems of evolution and biochemical information transfer. In: Kasha M, Pullman B (eds) Horizons in biochemistry. Academic Press, New York, pp 103–126

    Google Scholar 

  • Saenger W (1984) Principles of nucleic acid structure. Springer-Verlag, New York

    Google Scholar 

  • Schopf JW (ed) (1983) The Earth's earliest biosphere: its origin and evolution. Princeton Academic Press, Princeton NJ

    Google Scholar 

  • Schopf JW, Packer BM (1987) Early Archean (3.3 billion to 3.5 billion-year-old) microfossils from the Warrawoona group, Australia. Science 237:70–73

    PubMed  Google Scholar 

  • Schwartz AW (1986) Spontaneous oligomerization of purine derivatives. Abstracts of the Fifth ISSOL (International Society for the Study of the Origin of Life) Meeting, Berkeley CA, July 21–25, 1986, p 155

  • Schwartz AW (1987) Minimal requirements for molecular information transfer. Adv Space Res 6 (in press)

  • Schwartz AW, Orgel LE (1986) Template-directed synthesis of novel, nucleic acid-like structures. Science 228:585–587

    Google Scholar 

  • Setlow RB (1968) The photochemistry, photobiology and repair of polynucleotides. Prog Nucleic Acid Res Mol Biol 8:257–295

    PubMed  Google Scholar 

  • Shlomai J, Kornberg A (1978) Deoxyuridine triphosphatase ofEscherichia coli: purification, properties and use as a reagent to reduce uracil incorporation into DNA. J Biol Chem 253: 3305–3312

    PubMed  Google Scholar 

  • Shugar D (1960) Photochemistry of nucleic acids and their constituents. In: Chargaff E, Davidson JN (eds) The nucleic acids, vol III. Academic Press, New York, pp 39–104

    Google Scholar 

  • Singer B, Kusmierek JT (1982) Chemical mutagenesis. Annu Rev Biochem 52:655–693

    Google Scholar 

  • Spirin AS (1986) Ribosome structure and protein biosynthesis. Benjamin Cummings, Menlo Park CA

    Google Scholar 

  • Sprengel G, Follmann H (1981) Evidence for the reductive pathway of deoxyribonucleotide synthesis in an archaebacterium. FEBS Lett 132:207–209

    Google Scholar 

  • Springgate CF, Loeb LA (1975) On the fidelity of transcription by theEscherichia coli ribonucleic acid polymerase. J Mol Biol 97:577–591

    PubMed  Google Scholar 

  • Steinhauer DA, Holland JJ (1987) Rapid evolution of RNA viruses. Annu Rev Microbiol 41:409–433

    PubMed  Google Scholar 

  • Tye BK, Chien J, Lehman IR, Duncan BK, Warner HR (1978a) Uracil incorporation: a source of pulse-labeled DNA fragments in the replication of theEscherichia coli chromosome. Proc Natl Acad Sci USA 75:233–239

    PubMed  Google Scholar 

  • Tye BK, Nyman PO, Lehman IR (1978b) Excision repair of uracil during replication of ϕX 174 DNA in vitro. Biochem Biophys Res Commun 82:434–437

    PubMed  Google Scholar 

  • Usher DA (1977) Early chemical evolution of nucleic acids. Science 196:311–313

    PubMed  Google Scholar 

  • Varela F, Maturana HR (1974) Autopoiesis: the organization of living systems, its characterization and a model. Bio-Systems 5:187–196

    PubMed  Google Scholar 

  • Voet D, Gratzar WB, Cox RA, Doty P (1963) Absorption spectra of nucleotides, polynucleotides and nucleic acids in the far ultraviolet. Biopolymers 1:193–208

    Google Scholar 

  • Wacker A, Dellweg D, Trager L, Kornhauser A, Lodemann E, Turck G, Selzer R, Chandra P, Ishimoto M (1964) Organic photochemistry of nucleic acids. Photochem Photobiol 3:369–382

    Google Scholar 

  • White DH, Erickson JC (1981) Enhancement of peptide bond formation by polyribonucleotides on clay surfaces in fluctuating environments. J Mol Evol 17:19–26

    Google Scholar 

  • White HB (1976) Coenzymes as fossils of an earlier metabolic state. J Mol Evol 7:101–104

    PubMed  Google Scholar 

  • White HB (1982): Evolution of coenzymes and the origin of pyridine nucleotides. In: Everse J, Anderson B, You KS (eds) The pyridine nucleotide coenzymes. Academic Press, New York, pp 2–17

    Google Scholar 

  • Woese CR (1967) The origins of the genetic code. Harper and Row, New York

    Google Scholar 

  • Zaug, AJ, Cech TR (1985) Oligomerization of intervening sequence RNA molecules in the absence of proteins. Science 229:1060–1064.

    PubMed  Google Scholar 

  • Zaug, AJ, Cech TR (1986) The intervening sequences oftetrahymena is an enzyme. Science 231:470–475.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lazcano, A., Guerrero, R., Margulis, L. et al. The evolutionary transition from RNA to DNA in early cells. J Mol Evol 27, 283–290 (1988). https://doi.org/10.1007/BF02101189

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02101189

Key words

Navigation