RRC ID 3730
著者 Nakamura N, Morinaga H, Kikuchi M, Yonekura S, Ishii N, Yamamoto K, Yonei S, Zhang QM.
タイトル Cloning and characterization of uracil-DNA glycosylase and the biological consequences of the loss of its function in the nematode Caenorhabditis elegans.
ジャーナル Mutagenesis
Abstract Uracil arises in DNA from spontaneous deamination of cytosine and through incorporation of dUMP by DNA polymerase during DNA replication. Excision of uracil by the action of uracil-DNA glycosylase (Ung) initiates the base excision repair pathway to counter the promutagenic base modification. In this study, we cloned a cDNA-encoding Caenorhabditis elegans homologue (CeUng-1) of Escherichia coli Ung. There was 49% identity in amino acid sequence between E.coli Ung and CeUng-1. Purified CeUng-1 removed uracil from both U:G and U:A base pairs in DNA. It also removed uracil from single-stranded oligonucleotide substrate less efficiently than double-stranded oligonucleotide. The CeUng-1 activity was inhibited by Bacillus subtilis Ung inhibitor, indicating that CeUng-1 is a member of the family-1 Ung group. The mutation in the ung-1 gene did not affect development, fertility and lifespan in C.elegans, suggesting the existence of backup enzyme. However, we could not detect residual uracil excision activity in the extract derived from the ung-1 mutant. The present experiments also showed that the ung-1 mutant of C.elegans was more resistant to NaHSO(3)-inducing cytosine deamination than wild-type strain.
巻・号 23(5)
ページ 407-13
公開日 2008-9-1
DOI 10.1093/mutage/gen030
PII gen030
PMID 18524757
MeSH Amino Acid Sequence Animals Caenorhabditis elegans / drug effects Caenorhabditis elegans / enzymology* Caenorhabditis elegans / genetics Cloning, Molecular Conserved Sequence Cytosine / metabolism Deamination Molecular Sequence Data Mutation Protein Structure, Tertiary Sulfites / toxicity Uracil-DNA Glycosidase / genetics Uracil-DNA Glycosidase / metabolism*
IF 3.379
引用数 18
WOS 分野 TOXICOLOGY GENETICS & HEREDITY
リソース情報
線虫 tm2862