DNA bridging and looping by HMO1 provides a mechanism for stabilizing nucleosome-free chromatin

• Published in: Nucleic acids research 2014-08, Vol.42 (14), p.8996-9004
• Main Authors: Murugesapillai, Divakaran, McCauley, Micah J, Huo, Ran, Nelson Holte, Molly H, Stepanyants, Armen, Maher, 3rd, L James, Israeloff, Nathan E, Williams, Mark C
• Format: Article
• Language: English
• Subjects: Chromatin - chemistry; DNA - chemistry; DNA - metabolism; DNA - ultrastructure; Gene regulation, Chromatin and Epigenetics; High Mobility Group Proteins - metabolism; Nucleic Acid Conformation; Nucleosomes - chemistry; Saccharomyces cerevisiae Proteins - metabolism
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gku635

The regulation of chromatin structure in eukaryotic cells involves abundant architectural factors such as high mobility group B (HMGB) proteins. It is not understood how these factors control the interplay between genome accessibility and compaction. In vivo, HMO1 binds the promoter and coding regions of most ribosomal RNA genes, facilitating transcription and possibly stabilizing chromatin in the absence of histones. To understand how HMO1 performs these functions, we combine single molecule stretching and atomic force microscopy (AFM). By stretching HMO1-bound DNA, we demonstrate a hierarchical organization of interactions, in which HMO1 initially compacts DNA on a timescale of seconds, followed by bridge formation and stabilization of DNA loops on a timescale of minutes. AFM experiments demonstrate DNA bridging between strands as well as looping by HMO1. Our results support a model in which HMO1 maintains the stability of nucleosome-free chromatin regions by forming complex and dynamic DNA structures mediated by protein-protein interactions.