Action-at-a-distance mutations induced by 8-oxo-7,8-dihydroguanine are dependent on APOBEC3

© The Author(s) 2023. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com..

DNA oxidation is a serious threat to genome integrity and is involved in mutations and cancer initiation. The G base is most frequently damaged, and 8-oxo-7,8-dihydroguanine (GO, 8-hydroxyguanine) is one of the predominant damaged bases. In human cells, GO causes a G:C→T:A transversion mutation at the modified site, and also induces untargeted substitution mutations at the G bases of 5'-GpA-3' dinucleotides (action-at-a-distance mutations). The 5'-GpA-3' sequences are complementary to the 5'-TpC-3' sequences, the preferred substrates for apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3 (APOBEC3) cytosine deaminases, and thus their contribution to mutagenesis has been considered. In this study, APOBEC3B, the most abundant APOBEC3 protein in human U2OS cells, was knocked down in human U2OS cells, and a GO-shuttle plasmid was then transfected into the cells. The action-at-a-distance mutations were reduced to ~25% by the knockdown, indicating that GO-induced action-at-a-distance mutations are highly dependent on APOBEC3B in this cell line.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:39

Enthalten in:

Mutagenesis - 39(2024), 1 vom: 08. Feb., Seite 24-31

Sprache:

Englisch

Beteiligte Personen:

Fukushima, Ruriko [VerfasserIn]
Suzuki, Tetsuya [VerfasserIn]
Kobayakawa, Akari [VerfasserIn]
Kamiya, Hiroyuki [VerfasserIn]

Links:

Volltext

Themen:

5614-64-2
5Z93L87A1R
8-hydroxyguanine
8-oxo-7,8-dihydroguanine
9007-49-2
APOBEC3
APOBEC3B protein, human
Action-at-a-distance mutation
Cytidine Deaminase
Cytosine deaminase
DNA
EC 3.5.4.5
Guanine
Journal Article
Minor Histocompatibility Antigens

Anmerkungen:

Date Completed 09.02.2024

Date Revised 09.02.2024

published: Print

Citation Status MEDLINE

doi:

10.1093/mutage/gead023

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM359717128