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Accurate identification of 8-oxoguanine in RNA with single-nucleotide resolution using ligase-dependent qPCR.
Ye, Xidong; Li, Zengguang; Ye, Shangde; Liang, Xinqi; Bao, Chenyu; He, Mingyang; Wang, Hailan; Xia, Laixin; Cao, Xin.
Afiliação
  • Ye X; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Li Z; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Ye S; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Liang X; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Bao C; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • He M; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Wang H; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Xia L; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
  • Cao X; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China. cx123@smu.edu.cn.
Org Biomol Chem ; 22(27): 5629-5635, 2024 07 10.
Article em En | MEDLINE | ID: mdl-38912549
ABSTRACT
8-oxoguanine (o8G), a prevalent oxidative modification in RNA induced by reactive oxygen species (ROS), plays a pivotal role in regulating RNA functions. Accurate detection and quantification of o8G modifications is critical to understanding their biological significance and potential as disease biomarkers, but effective detection methods remain limited. Here, we have developed a highly specific T3 DNA ligase-dependent qPCR assay that exploits the enzyme's ability to discriminate o8G from guanine (G) with single-nucleotide resolution. This method can detect o8G in RNA at levels as low as 500 fM, with an up to 18-fold higher selectivity for discriminating o8G from G. By simulating oxidative stress conditions in SH-SY5Y and HS683 cell lines treated with rotenone, we successfully identified site-specific o8G modifications in key miRNAs associated with neuroprotective responses, including miR-124, let-7a and miR-29a. The developed assay holds significant promise for the practical identification of o8G, facilitating its potential for detailed studies of o8G dynamics in various biological contexts and diseases.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Guanina Limite: Humans Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Guanina Limite: Humans Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China