MADDD-seq, a novel massively parallel sequencing tool for simultaneous detection of DNA damage and mutations

Author:

Vermulst Marc1ORCID,Paskvan Samantha L2,Chung Claire S1,Franke Kathryn2,Clegg Nigel2,Minot Sam3,Madeoy Jennifer2,Long Annalyssa S2,Gout Jean-Francois4,Bielas Jason H25

Affiliation:

1. University of Southern California, Leonard Davis School of Gerontology , Los Angeles , CA , USA

2. Translational Research Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA

3. Data Core, Fred Hutchinson Cancer Research Center , Seattle , WA , USA

4. Department of Biological Sciences, Mississippi State University , Mississippi State, MS,  USA

5. Department of Laboratory Medicine and Pathology, University of Washington , Seattle , WA , USA

Abstract

Abstract Our genome is exposed to a wide variety of DNA-damaging agents. If left unrepaired, this damage can be converted into mutations that promote carcinogenesis or the development of genetically inherited diseases. As a result, researchers and clinicians require tools that can detect DNA damage and mutations with exceptional sensitivity. In this study, we describe a massively parallel sequencing tool termed Mutation And DNA Damage Detection-seq (MADDD-seq) that is capable of detecting O6-methyl guanine lesions and mutations simultaneously, with a single assay. To illustrate the dual capabilities of MADDD-seq, we treated WT and DNA repair deficient yeast cells with the DNA-damaging agent MNNG and tracked DNA lesions and mutations over a 24-h time period. This approach allowed us to identify thousands of DNA adducts and mutations in a single sequencing run and gain deep insight into the kinetics of DNA repair and mutagenesis.

Funder

National Institute on Aging

National Cancer Institute

National Institute of Environmental Health Sciences

University of Southern California

Publisher

Oxford University Press (OUP)

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