Related Experiment Video
Updated: Aug 6, 2026

CD Spectroscopy to Study DNA-Protein Interactions
Published on: February 10, 2022
DNA methyltransferase probing of DNA-protein interactions
Scott A Hoose1, Michael P Kladde
1Department of Biochemistry and Biophysics, Texas A & M University, College Station, TX, USA.
Abstract:
Effective methods of probing chromatin structure without disrupting DNA-protein interactions and associations are necessary for creating an accurate picture of chromatin and its processes in vivo. Expression of cytidine-5 DNA methyltransferases (C5 DMTases) in Saccharomyces cerevisiae provides a powerful noninvasive method of assaying relative DNA accessibility in chromatin. DNA MTases are occluded from protein-associated DNA based on the strength and span of the DNA-protein interaction. Ectopic regulation of C5 DMTase expression systems allows for minimal disruption of yeast physiology. Methylated sites are detected by bisulfite genomic sequencing, which leads to a positive signal corresponding to modified cytidine residues. High-resolution C5 DMTases with dinucleotide recognition specificity are shown to provide sufficient coverage to map interactions spanning a relatively short distance.

