Abstract
Chromatin remodelers are complexes able to both alter histone-DNA interactions and to mobilize nucleosomes. The mechanism of their action and the conformation of remodeled nucleosomes remain a matter of debates. In this work we compared the type and structure of the products of nucleosome remodeling by SWI/SNF and ACF complexes using high-resolution microscopy combined with novel biochemical approaches. We find that SWI/SNF generates a multitude of nucleosome-like metastable particles termed “remosomes”. Restriction enzyme accessibility assay, DNase I footprinting and AFM experiments reveal perturbed histone-DNA interactions within these particles. Electron cryo-microscopy shows that remosomes adopt a variety of different structures with variable irregular DNA path, similar to those described upon RSC remodeling. Remosome DNA accessibility to restriction enzymes is also markedly increased. We suggest that the generation of remosomes is a common feature of the SWI/SNF family remodelers. In contrast, the ACF remodeler, belonging to ISWI family, only produces repositioned nucleosomes and no evidence for particles associated with extra DNA, or perturbed DNA paths was found. The remosome generation by the SWI/SNF type of remodelers may represent a novel mechanism involved in processes where nucleosomal DNA accessibility is required, such as DNA repair or transcription regulation.
Highlights
Structured domain and non-structured, highly flexible NH2-termini, which protrude from the nucleosome
In this work we have made a detailed comparison of the type and structure of the products of nucleosome remodeling by SWI/SNF and ACF using high-resolution microscopy methods combined with novel biochemical approaches
Electron cryo-microscopy visualization of the remosomes shows that they are larger than standard nucleosomes and that they adopt a variety of different structures
Summary
Structured domain and non-structured, highly flexible NH2-termini, which protrude from the nucleosome. To analyze the perturbations in the histone-DNA interactions within the SWI/SNF treated particles, we have used a recently developed approach, termed “in gel one pot assay” (see Fig. 2 and[42]).
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