Polymerase-tautomeric Model for Untargeted Delayed Base Substitution Mutations Formation during Error-prone and SOS Replication of Double-stranded DNA Containing Thymine and Adenine in Some Rare Tautomeric Forms

Authors

  • Helen A. Grebneva Donetsk Physical and Technical Institute, National Academy of Science of Ukraine, 03680 Kiev, Nauky av. 46, Ukraine,

DOI:

https://doi.org/10.30564/jor.v1i2.1584

Abstract

Polymerase-tautomeric model for untargeted delayed base substitution mutations is proposed. Structural analysis of bases insertion showed that any canonical bases may be inserted opposite rare tautomeric forms of thymine T3*, adenines A2* and A4* so that between them hydrogen bonds are formed. Canonical adenine and cytosine can be incorporated opposite canonical thymine only. Canonical thymine and guanine can be incorporated opposite canonical adenine only. If in the synthesis of DNA containing rare tautomeric forms of thymine T3*, adenines A2* and A4*, involved DNA polymerases with relatively high fidelity of synthesis, mutations not appear. However, if further DNA synthesis will involve DNA polymerases having a low fidelity of synthesis, there may be base substitution mutations. It was shown that the conclusion made in the Tomasetti and Vogelstein cancer risk model that the formation of about 67% of all mutations was not caused by exposure to any mutagens is erroneous. 

Keywords:

Radiation-induced genomic instability, Untargeted delayed base substitution mutations, UV-mutagenesis, Rare tautomeric forms of DNA bases, Thymine, adenine, Error-prone replication, SOS replication

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Grebneva, H. A. (2019). Polymerase-tautomeric Model for Untargeted Delayed Base Substitution Mutations Formation during Error-prone and SOS Replication of Double-stranded DNA Containing Thymine and Adenine in Some Rare Tautomeric Forms. Journal of Oncology Research, 1(2), 24–37. https://doi.org/10.30564/jor.v1i2.1584

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