Cargando…
Eukaryotic Y-family polymerases bypass a 3-methyl-2′-deoxyadenosine analog in vitro and methyl methanesulfonate-induced DNA damage in vivo
N3-methyl-adenine (3MeA) is the major cytotoxic lesion formed in DNA by S(N)2 methylating agents. The lesion presumably blocks progression of cellular replicases because the N3-methyl group hinders interactions between the polymerase and the minor groove of DNA. However, this hypothesis has yet to b...
Autores principales: | Plosky, Brian S., Frank, Ekaterina G., Berry, David A., Vennall, Graham P., McDonald, John P., Woodgate, Roger |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367705/ https://www.ncbi.nlm.nih.gov/pubmed/18281311 http://dx.doi.org/10.1093/nar/gkn058 |
Ejemplares similares
-
Roles of PCNA ubiquitination and TLS polymerases κ and η in the bypass of methyl methanesulfonate-induced DNA damage
por: Wit, Niek, et al.
Publicado: (2015) -
Activation of a Mitogen-Activated Protein Kinase Hog1 by DNA Damaging Agent Methyl Methanesulfonate in Yeast
por: Huang, Shan, et al.
Publicado: (2020) -
Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus
por: Vaisman, Alexandra, et al.
Publicado: (2021) -
Corrigendum: Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus
por: Vaisman, Alexandra, et al.
Publicado: (2021) -
The exploration of N6-deoxyadenosine methylation in mammalian genomes
por: Li, Xuwen, et al.
Publicado: (2021)