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http://purl.uniprot.org/citations/25063301http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25063301http://www.w3.org/2000/01/rdf-schema#comment"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."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.org/dc/terms/identifier"doi:10.1093/nar/gku635"xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Williams M.C."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Huo R."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Maher L.J."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"McCauley M.J."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Israeloff N.E."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Murugesapillai D."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Nelson Holte M.H."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/author"Stepanyants A."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/name"Nucleic Acids Res"xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/pages"8996-9004"xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/title"DNA bridging and looping by HMO1 provides a mechanism for stabilizing nucleosome-free chromatin."xsd:string
http://purl.uniprot.org/citations/25063301http://purl.uniprot.org/core/volume"42"xsd:string
http://purl.uniprot.org/citations/25063301http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/25063301
http://purl.uniprot.org/citations/25063301http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/25063301
http://purl.uniprot.org/uniprot/Q03973#attribution-560C3832603ECB081DA13875B13B006Ahttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/25063301
http://purl.uniprot.org/uniprot/#_Q03973-mappedCitation-25063301http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25063301
http://purl.uniprot.org/uniprot/Q03973http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25063301