Bowhead NEIL1: molecular cloning, characterization, and enzymatic properties.


Journal

Biochimie
ISSN: 1638-6183
Titre abrégé: Biochimie
Pays: France
ID NLM: 1264604

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 24 08 2022
revised: 19 10 2022
accepted: 25 10 2022
pubmed: 6 11 2022
medline: 25 2 2023
entrez: 5 11 2022
Statut: ppublish

Résumé

Nei Like DNA Glycosylase 1 (NEIL1) is a DNA glycosylase, which specifically processes oxidative DNA damage by initiating base excision repair. NEIL1 recognizes and removes bases, primarily oxidized pyrimidines, which have been damaged by endogenous oxidation or exogenous mutagenic agents. NEIL1 functions through a combined glycosylase/AP (apurinic/apyrimidinic)-lyase activity, whereby it cleaves the N-glycosylic bond between the DNA backbone and the damaged base via its glycosylase activity and hydrolysis of the DNA backbone through beta-delta elimination due to its AP-lyase activity. In our study we investigated our hypothesis proposing that the cancer resistance of the bowhead whale can be associated with a better DNA repair with NEIL1 being upregulated or more active. Here, we report the molecular cloning and characterization of three transcript variants of bowhead whale NEIL1 of which two were homologous to human transcripts. In addition, a novel NEIL1 transcript variant was found. A differential expression of NEIL mRNA was detected in bowhead eye, liver, kidney, and muscle. The A-to-I editing of NEIL1 mRNA was shown to be conserved in the bowhead and two adenosines in the 242Lys codon were subjected to editing. A mass spectroscopy analysis of liver and eye tissue failed to demonstrate the existence of a NEIL1 isoform originating from RNA editing. Recombinant bowhead and human NEIL1 were expressed in E. coli and assayed for enzymatic activity. Both bowhead and human recombinant NEIL1 catalyzed, with similar efficiency, the removal of a 5-hydroxyuracil lesion in a DNA bubble structure. Hence, these results do not support our hypothesis but do not refute the hypothesis either.

Identifiants

pubmed: 36334646
pii: S0300-9084(22)00280-2
doi: 10.1016/j.biochi.2022.10.014
pii:
doi:

Substances chimiques

DNA Glycosylases EC 3.2.2.-
DNA 9007-49-2
RNA, Messenger 0
Lyases EC 4.-
NEIL1 protein, human EC 3.2.2.-
Nei protein, E coli EC 3.1.25.1
Escherichia coli Proteins 0
Deoxyribonuclease (Pyrimidine Dimer) EC 3.1.25.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

136-149

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Signe Holm (S)

Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, DK-8000, Aarhus C, Denmark.

Rikke Møller Larsen (RM)

Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, DK-8000, Aarhus C, Denmark.

Camilla Myrup Holst (CM)

Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, DK-8000, Aarhus C, Denmark.

Mads Peter Heide-Jørgensen (MP)

Greenland Institute of Natural Resources, Strandgade 91, 2, DK-1401, Copenhagen K, Denmark.

John Fleng Steffensen (JF)

Marine Biological Section, University of Copenhagen, Strandpromenaden 5, DK-3000, Helsingør, Denmark.

Tinna Stevnsner (T)

Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, DK-8000, Aarhus C, Denmark.

Knud Larsen (K)

Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, DK-8000, Aarhus C, Denmark. Electronic address: Knud.Larsen@mbg.au.dk.

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Classifications MeSH