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Updated: Oct 19, 2025

The Lambda Select cII Mutation Detection System
Published on: April 26, 2018
Biochemical and photochemical mechanisms that produce different UV-induced mutation spectra
Tomohiko Sugiyama1, Brianna Keinard2, Griffin Best2
1Department of Biological Sciences; Molecular and Cellular Biology Graduate Program, Ohio University, Athens, OH, 45701, USA.
Abstract:
Although UV-induced mutagenesis has been studied extensively, the precise mechanisms that convert UV-induced DNA damage into mutations remain elusive. One well-studied mechanism involves DNA polymerase (Pol) η and ζ, which produces C > T transitions during translesion synthesis (TLS) across pyrimidine dimers. We previously proposed another biochemical mechanism that involves multiple UV-irradiations with incubation in the dark in between. The incubation facilitates spontaneous deamination of cytosine in a pyrimidine dimer, and the subsequent UV irradiation induces photolyase-independent (direct) photoreversal that converts cytosine into monomeric uracil residue. In this paper, we first demonstrate that natural sunlight can induce both mutational processes in vitro. The direct photoreversal was also reproduced by monochromatic UVB at 300 nm. We also demonstrate that post-irradiation incubation in the dark is required for both mutational processes, suggesting that cytosine deamination is required for both the Pol η/ζ-dependent and the photoreversal-dependent mechanisms. Another Y-family polymerase Pol ι also mediated a mutagenic TLS on UV-damaged templates when combined with Pol ζ. The Pol ι-dependent mutations were largely independent of post-irradiation incubation, indicating that cytosine deamination was not essential for this mutational process. Sunlight-exposure also induced C > A transversions which were likely caused by oxidation of guanine residues. Finally, we constructed in vitro mutation spectra in a comparable format to cancer mutation signatures. While both Pol η-dependent and photoreversal-dependent spectra showed high similarities to a cancer signature (SBS7a), Pol ι-dependent mutation spectrum has distinct T > A/C substitutions, which are found in another cancer signature (SBS7d). The Pol ι-dependent T > A/C substitutions were resistant to T4 pyrimidine dimer glycosylase-treatment, suggesting that this mutational process is independent of cis-syn pyrimidine dimers. An updated model about multiple mechanisms of UV-induced mutagenesis is discussed.
Insights
Sunlight induces DNA mutations via multiple pathways, including polymerase action and direct photoreversal, with distinct mechanisms linked to specific cancer mutation signatures.
Area of Science:
- Molecular Biology
- Genetics
- Photochemistry
Background:
- UV radiation causes DNA damage, leading to mutations.
- DNA polymerases (Pol) η and ζ mediate translesion synthesis (TLS) across UV-induced pyrimidine dimers, primarily causing C>T transitions.
- A proposed mechanism involves UV-induced cytosine deamination followed by direct photoreversal.
Purpose of the Study:
- To investigate multiple mechanisms of UV-induced mutagenesis using natural sunlight and monochromatic UVB.
- To compare in vitro mutation spectra with known cancer mutation signatures.
- To elucidate the roles of different DNA polymerases and DNA repair pathways in UV mutagenesis.
Main Methods:
- In vitro experiments exposing DNA to natural sunlight and monochromatic UVB (300 nm).
- Incubation periods in the dark between UV exposures to facilitate deamination.
- Analysis of mutations generated by DNA polymerases (Pol) η, ζ, and ι.
- Assessment of resistance to T4 pyrimidine dimer glycosylase treatment.
Main Results:
- Natural sunlight and UVB induced both Pol η/ζ-dependent and photoreversal-dependent mutagenesis.
- Post-irradiation dark incubation was crucial for both mechanisms, indicating a role for cytosine deamination.
- Pol ι, combined with Pol ζ, generated mutations largely independent of dark incubation.
- Sunlight also induced C>A transversions, likely via guanine oxidation.
- Pol η/photoreversal spectra resembled cancer signature SBS7a, while Pol ι spectra showed T>A/C substitutions characteristic of SBS7d.
Conclusions:
- Multiple biochemical pathways contribute to UV-induced mutagenesis.
- Cytosine deamination is a key step in both Pol η/ζ-dependent and photoreversal-dependent mutagenesis.
- Pol ι-dependent mutagenesis, independent of cis-syn pyrimidine dimers, contributes to distinct cancer mutation signatures.
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