Complementary base pairing and the origin of substitution mutations View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1976-09

AUTHORS

Michael D. Topal, Jacques R. Fresco

ABSTRACT

On the basis of chemical considerations and model building, the Watson-Crick concept of complementary base pairing is extended to a wider range of DNA pairs that A-T and G-C (including A-C, G-T, A-A, G-G and G-A) by invoking imino or enol tautomers (or protonated species) and synisomers. The virtual absence of these additional base pairs from DNA is explained in terms of the low frequency with which these unfavoured forms occur and the two-step mechanism of DNA synthesis, whereby residues are first incorporated by the DNA polymerase and then checked. This base-pairing hypothesis is used to explain the origin, nature and level of spontaneous substitution mutations, their enhancement by base analogues, and the unique effects of certain mutator alleles. More... »

PAGES

285-289

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/263285a0

DOI

http://dx.doi.org/10.1038/263285a0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1023822148

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/958482


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