Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties

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 func...

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Published in:Biochimie
Main Authors: Holm, Signe, Larsen, Rikke Møller, Holst, Camilla Myrup, Heide-Jørgensen, Mads Peter, Steffensen, John Fleng, Stevnsner, Tinna, Larsen, Knud
Format: Article in Journal/Newspaper
Language:English
Published: 2023
Subjects:
DNA
RNA
Online Access:https://pure.au.dk/portal/en/publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18
https://doi.org/10.1016/j.biochi.2022.10.014
id ftuniaarhuspubl:oai:pure.atira.dk:publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18
record_format openpolar
spelling ftuniaarhuspubl:oai:pure.atira.dk:publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18 2024-02-11T10:02:36+01:00 Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties Holm, Signe Larsen, Rikke Møller Holst, Camilla Myrup Heide-Jørgensen, Mads Peter Steffensen, John Fleng Stevnsner, Tinna Larsen, Knud 2023-03 https://pure.au.dk/portal/en/publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18 https://doi.org/10.1016/j.biochi.2022.10.014 eng eng https://pure.au.dk/portal/en/publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18 info:eu-repo/semantics/openAccess Holm , S , Larsen , R M , Holst , C M , Heide-Jørgensen , M P , Steffensen , J F , Stevnsner , T & Larsen , K 2023 , ' Bowhead NEIL1 : molecular cloning, characterization, and enzymatic properties ' , Biochimie , vol. 206 , pp. 136-149 . https://doi.org/10.1016/j.biochi.2022.10.014 Aging Base excision repair Bowhead NEIL1 RNA editing DNA Glycosylases/genetics Humans Escherichia coli/genetics Deoxyribonuclease (Pyrimidine Dimer)/genetics Animals DNA DNA Repair Cloning Molecular Lyases/metabolism Escherichia coli Proteins/genetics Bowhead Whale/genetics RNA Messenger article 2023 ftuniaarhuspubl https://doi.org/10.1016/j.biochi.2022.10.014 2024-01-18T00:00:56Z 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. Article in Journal/Newspaper bowhead whale Aarhus University: Research Biochimie
institution Open Polar
collection Aarhus University: Research
op_collection_id ftuniaarhuspubl
language English
topic Aging
Base excision repair
Bowhead
NEIL1
RNA editing
DNA Glycosylases/genetics
Humans
Escherichia coli/genetics
Deoxyribonuclease (Pyrimidine Dimer)/genetics
Animals
DNA
DNA Repair
Cloning
Molecular
Lyases/metabolism
Escherichia coli Proteins/genetics
Bowhead Whale/genetics
RNA
Messenger
spellingShingle Aging
Base excision repair
Bowhead
NEIL1
RNA editing
DNA Glycosylases/genetics
Humans
Escherichia coli/genetics
Deoxyribonuclease (Pyrimidine Dimer)/genetics
Animals
DNA
DNA Repair
Cloning
Molecular
Lyases/metabolism
Escherichia coli Proteins/genetics
Bowhead Whale/genetics
RNA
Messenger
Holm, Signe
Larsen, Rikke Møller
Holst, Camilla Myrup
Heide-Jørgensen, Mads Peter
Steffensen, John Fleng
Stevnsner, Tinna
Larsen, Knud
Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
topic_facet Aging
Base excision repair
Bowhead
NEIL1
RNA editing
DNA Glycosylases/genetics
Humans
Escherichia coli/genetics
Deoxyribonuclease (Pyrimidine Dimer)/genetics
Animals
DNA
DNA Repair
Cloning
Molecular
Lyases/metabolism
Escherichia coli Proteins/genetics
Bowhead Whale/genetics
RNA
Messenger
description 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.
format Article in Journal/Newspaper
author Holm, Signe
Larsen, Rikke Møller
Holst, Camilla Myrup
Heide-Jørgensen, Mads Peter
Steffensen, John Fleng
Stevnsner, Tinna
Larsen, Knud
author_facet Holm, Signe
Larsen, Rikke Møller
Holst, Camilla Myrup
Heide-Jørgensen, Mads Peter
Steffensen, John Fleng
Stevnsner, Tinna
Larsen, Knud
author_sort Holm, Signe
title Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
title_short Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
title_full Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
title_fullStr Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
title_full_unstemmed Bowhead NEIL1:molecular cloning, characterization, and enzymatic properties
title_sort bowhead neil1:molecular cloning, characterization, and enzymatic properties
publishDate 2023
url https://pure.au.dk/portal/en/publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18
https://doi.org/10.1016/j.biochi.2022.10.014
genre bowhead whale
genre_facet bowhead whale
op_source Holm , S , Larsen , R M , Holst , C M , Heide-Jørgensen , M P , Steffensen , J F , Stevnsner , T & Larsen , K 2023 , ' Bowhead NEIL1 : molecular cloning, characterization, and enzymatic properties ' , Biochimie , vol. 206 , pp. 136-149 . https://doi.org/10.1016/j.biochi.2022.10.014
op_relation https://pure.au.dk/portal/en/publications/12d6afaf-4bdb-4e55-b53e-0bd8bc6d0f18
op_rights info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.1016/j.biochi.2022.10.014
container_title Biochimie
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