Evidence map›Paper›PMID 31578361›Full record

ArticleScientific reports2019

Generation of Remosomes by the SWI/SNF Chromatin Remodeler Family.

Manu Shubhdarshan Shukla, Sajad Hussain Syed, Ramachandran Boopathi, Elsa Ben Simon, Sunil Nahata, Lorrie Ramos, Defne Dalkara, Cendrine Moskalenko, Andrew Travers, Dimitar Angelov and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 3 countries.

Manu Shubhdarshan ShuklaUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France. v1mshukl@exseed.ed.ac.uk.
Sajad Hussain SyedUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France.
Ramachandran BoopathiUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France.
Elsa Ben SimonUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France.
Sunil NahataUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France.
Lorrie RamosUniversité Grenoble Alpes, CNRS UMR 5309, INSERM U1209, Institute for Advanced Biosciences (IAB), Site Santé - Allée des Alpes, 38700, La Tronche, France.
Defne DalkaraUniversité Grenoble Alpes, CNRS UMR 5309, INSERM U1209, Institute for Advanced Biosciences (IAB), Site Santé - Allée des Alpes, 38700, La Tronche, France.
Cendrine MoskalenkoLaboratoire de Physique, UMR 5672, CNRS, Université de Lyon 1, Ecole Normale Supérieure de Lyon, 69364, Lyon, cedex 07, France.
Andrew TraversMRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK.
Dimitar AngelovUniversité de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, CNRS-UMR 5239, Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364, Lyon, cedex 07, France.
Stefan DimitrovUniversité Grenoble Alpes, CNRS UMR 5309, INSERM U1209, Institute for Advanced Biosciences (IAB), Site Santé - Allée des Alpes, 38700, La Tronche, France.
Ali HamicheInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, Parc d'innovation, 1 rue Laurent Fries, 67404, Ilkirch, Cedex, France. hamiche@igbmc.fr.
Jan BednarUniversité Grenoble Alpes, CNRS UMR 5309, INSERM U1209, Institute for Advanced Biosciences (IAB), Site Santé - Allée des Alpes, 38700, La Tronche, France. jan.bednar@univ-grenoble-alpes.fr.
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105178783
6 · The paper itself

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.

Indexed as

Adenosine TriphosphateAnimalsCell-Free SystemChromatin Assembly and DisassemblyChromosomal Proteins, Non-HistoneDeoxyribonucleases, Type II Site-SpecificDNA, BacterialDNA FootprintingFungal ProteinsHistonesMicroscopy, Atomic ForceMultiprotein ComplexesNucleosomesPlasmidsRecombinant ProteinsRNA-Binding ProteinsAdenosine TriphosphateChromosomal Proteins, Non-HistoneDeoxyribonucleases, Type II Site-SpecificDNA, BacterialFungal ProteinsGGCC-specific type II deoxyribonucleasesHistonesMultiprotein ComplexesNucleosomesRecombinant ProteinsRNA-Binding Proteins

Identifiers

PMID31578361
PMCPMC6775096
OpenAlexW2978829870

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.