Cited by 149DNA and Nucleic Acid ChemistryRNA and protein synthesis mechanismsAdvanced biosensing and bioanalysis techniques

Nonenzymatic synthesis of oligoadenylates on a polyuridylic acid template.

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Sulston, J, Lohrmann, R, Orgel, L E, Miles, H T·1968·Proceedings of the National Academy of Sciences

Abstract

A number of nucleosides and mononucleotides have been shown to interact with complementary polynucleotides to form ordered helices of welldefined stoichiometry.1-3These latter are believed to have structures closely resembling those formed by corresponding pairs of polynucleotides.The condensation of preformed hexathymidylate residues to the dodecadeoxynucleotide in the presence of polyadenylic acid has already been reported.4We shall show that this reaction can be extended to the monomers adenosine and adenylic acid when they are incorporated in an ordered helix with poly U.Experimental and Results.-(a)Physical methods: Paper chromatography was carried out on Whatman 3 MM paper by the descending technique.The solvent systems were: I, isopropanol-concentrated ammonia-water (7:1:2, v/v); II, n-propanol-concentrated ammonia-water (55:10: 35, v/v); III, saturated aqueous ammonium sulphate-0.1 M sodium acetate-isopropanol (79:19:2, v/v); VIII, n-butanol-5 M acetic acid (2: 1, v/v).Thin-layer chromatography (system IV) was performed on Brinkmann MN-Polygram Cel 300 PEI, by the ascend- ing technique.5The sheets (20 X 20 cm) were prewashed with water and air- dried before application of substrate; they were developed for one hour in 0.5 M NaCl, then for two to three hours in 1.0 M NaCl.A paper wick applied to the upper edge allowed the solvent front to overrun.Paper electrophoresis was carried out on Whatman 3 MM paper, using varsol or CCl4 as coolant.The buf- fers were: V, potassium phosphate, 0.03 M, pH 7.1; VI, formic acid-ammonium formate, 0.05 M, pH 2.6; VII, sodium borate, 0.05 M, pH 9.0.-Chromatographic and electrophoretic data are collected in Tables 1 and2.Chromatograms and electrophoretograms of radioactive samples were cut into strips and passed through a Baird-Atomic RSC-363 scanner, to give a graphic record.Relevant areas were cut out and their radioactivities measured more precisely in a liquid scintillation system (Beckman LS-200).The papers were placed directly in Liquifluor diluted with toluene.(b) Materials: Poly U was obtained from Schwarz BioResearch.Before use, it was dialyzed against 0.5 M NaCl, then against distilled water, and finally lyophilized in order to yield the sodium salt, free of small molecules.The product was checked for oligomers in system II and found to contain none.Nucleo- sides and nucleotides, including those isotopically labeled, were supplied by Schwarz.

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  • No extension of primer 2 by GMP was detectable with EDC alone, even in high-salt buffer containing 0.8 m EDC.

    “Initially, no extension of primer 2 by GMP was detectable, even in high-salt buffer containing 0.8 m EDC, and our experimental work aimed at high-yielding reactions was unsuccessful, in agreement with the low yields reported in the early literature.”

    From Copying of RNA Sequences without Pre‐Activation (2015) · cites this paper as [30]

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Authors
Sulston, J., Lohrmann, R., Orgel, L. E., & Miles, H. T.
Affiliations
National Institutes of Health (US)
Venue
Proceedings of the National Academy of Sciences
Published
1968-03
Volume
59
Issue
3
Pages
726-733
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2068866177
Cited by
149
References
0
Citations by year
2025: 7 · 2024: 4 · 2023: 5 · 2022: 3 · 2021: 5 · 2020: 4 · 2019: 6 · 2018: 5 · 2017: 4 · 2016: 3 · 2015: 6 · 2014: 3 · 2013: 1 · 2012: 4
FWCI
1.30
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced biosensing and bioanalysis techniques
Keywords
oligoadenylates, nucleoside incorporation, adenosine, adenosine monophosphate, oligonucleotide synthesis, nucleic acid hybridization
MeSH terms
Adenine Nucleotides, Chromatography, Thin Layer, Electrophoresis, Polynucleotides, Templates, Genetic, Uracil Nucleotides

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