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Nucleic Acids Res ; 30(2): 569-73, 2002 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-11788720

RESUMO

To elucidate the response to oxidative stress in eukaryotic cells, the effect of an oxidized nucleotide, 8-oxo-2'-deoxyguanosine 5'-triphosphate (8-oxo-dGTP), generated from dGTP with an active oxygen, on DNA synthesis was studied using a cell-free DNA replication system derived from Xenopus egg lysates with a single-stranded DNA template. Amounts of newly synthesized DNA were reduced according to the increasing concentration of 8-oxo-dGTP. Pulse labeling analysis revealed that 8-oxo-dGTP could delay DNA synthesis by reducing the rate of chain elongation. This delay was recovered by addition of a protein kinase inhibitor, staurosporine or bisindolylmaleimide I. These results indicate that a staurosporine- or bisindolylmaleimide I-sensitive protein kinase, such as a protein kinase C family member, may contribute to the delay of DNA synthesis by 8-oxo-dGTP. UV-irradiated single-stranded DNA also caused a delay of DNA synthesis on the undamaged template in the lysates. However, this delay was not recovered by staurosporine or bisindolylmaleimide I. Therefore, the mechanism of delay of DNA synthesis by 8-oxo-dGTP may be different from that by UV lesions. This is the first report that demonstrates an effect of an oxidized nucleotide on DNA replication in eukaryotes.


Assuntos
Replicação do DNA , Nucleotídeos de Desoxiguanina/metabolismo , Oócitos/enzimologia , Proteínas Quinases/metabolismo , Xenopus/metabolismo , Animais , Extratos Celulares , Sistema Livre de Células/efeitos dos fármacos , Dano ao DNA/efeitos da radiação , Replicação do DNA/efeitos dos fármacos , DNA de Cadeia Simples/biossíntese , DNA de Cadeia Simples/efeitos da radiação , Nucleotídeos de Desoxiguanina/farmacologia , Ativação Enzimática/efeitos dos fármacos , Feminino , Indóis/farmacologia , Cinética , Maleimidas/farmacologia , Oócitos/citologia , Oócitos/metabolismo , Estresse Oxidativo , Proteína Quinase C/antagonistas & inibidores , Proteína Quinase C/metabolismo , Inibidores de Proteínas Quinases , Estaurosporina/farmacologia , Moldes Genéticos
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