Cargando…
Handling the 3-methylcytosine lesion by six human DNA polymerases members of the B-, X- and Y-families
Alkylating agents often generate 3-methylcytosine (3meC) lesions that are efficiently repaired by AlkB homologues. If AlkB homologue proteins are not functional, or the number of 3meC lesions exceeds the cellular repair capacity, the damage will persist in the genome and become substrate of DNA poly...
Autores principales: | Furrer, Antonia, van Loon, Barbara |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874200/ https://www.ncbi.nlm.nih.gov/pubmed/24097443 http://dx.doi.org/10.1093/nar/gkt889 |
Ejemplares similares
-
5-methylcytosine-sensitive variants of Thermococcus kodakaraensis DNA polymerase
por: Huber, Claudia, et al.
Publicado: (2016) -
A discontinuous DNA glycosylase domain in a family of enzymes that excise 5-methylcytosine
por: Ponferrada-Marín, María Isabel, et al.
Publicado: (2011) -
Noncanonical prokaryotic X family DNA polymerases lack polymerase activity and act as exonucleases
por: Prostova, Maria, et al.
Publicado: (2022) -
Mechanism of double-base lesion bypass catalyzed by a Y-family DNA polymerase
por: Brown, Jessica A., et al.
Publicado: (2008) -
Recognition and cleavage of 5-methylcytosine DNA by bacterial SRA-HNH proteins
por: Han, Tiesheng, et al.
Publicado: (2015)