A novel method for monitoring functional lesion-specific recruitment of repair proteins in live cells

作者：Woodrick Jordan; Gupta Suhani; Khatkar Pooja; Dave Kalpana; Levashova Darya; Choudhury Sujata; Elias Hadi; Saha Tapas; Mueller Susette; Roy Rabindra^*

来源：Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis, 2015, 775: 48-58.

DOI：10.1016/j.mrfmmm.2015.03.013

• DNA-protein interaction
• Base excision repair
• Abasic sites
• Repair intermediate
• Co-localization

DNA-protein relationships have been studied by numerous methods, but a particular gap in methodology lies in the study of DNA adduct-specific interactions with proteins in vivo, which particularly affects the field of DNA repair. Using the repair of a well-characterized and ubiquitous adduct, the abasic (AP) site, as a model, we have developed a comprehensive method of monitoring DNA lesion-specific recruitment of proteins in vivo over time. We utilized a surrogate system in which a Cy3-labeled plasmid containing a single AP-site was transfected into cells, and the interaction of the labeled DNA with BER enzymes, including APE1, Pol beta, LIG1, and FEN1, was monitored by immunofluorescent staining of the enzymes by Alexafluor-488-conjugated secondary antibody. The recruitment of enzymes was characterized by quantification of Cy3-Alexafluor-488 co-localization. To validate the microscopy-based method, repair of the transfected AP-site DNA was also quantified at various time points post-transfection using a real time PCR-based method. Notably, the recruitment time kinetics for each enzyme were consistent with AP-site repair time kinetics. This microscopy-based methodology is reliable in detecting the recruitment of proteins to specific DNA substrates and can be extended to study other in vivo DNA-protein relationships in any DNA sequence and in the context of any DNA structure in transfectable proliferating or quiescent cells. The method may be applied to a variety of disciplines of nucleic acid transaction pathways, including repair, replication, transcription, and recombination.

• 出版日期2015-5