Evidence map›Paper›PMID 32220303›Full record

ArticleMolecular cell2020

4D Genome Rewiring during Oncogene-Induced and Replicative Senescence.

Satish Sati, Boyan Bonev, Quentin Szabo, Daniel Jost, Paul Bensadoun, Francois Serra, Vincent Loubiere, Giorgio Lucio Papadopoulos, Juan-Carlos Rivera-Mulia, Lauriane Fritsch and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 166 citations in OpenAlex.

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46 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 11 institutions in 3 countries.

Satish SatiInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France; Institute for Regenerative Medicine and Biotherapy, Univ Montpellier, INSERM UMR1183, F-34295 Montpellier, France.
Boyan BonevInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Quentin SzaboInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Daniel JostUniv Grenoble Alpes, CNRS, Grenoble INP, TIMC-IMAG, 38000 Grenoble, France.
Paul BensadounInstitute for Regenerative Medicine and Biotherapy, Univ Montpellier, INSERM UMR1183, F-34295 Montpellier, France.
Francois SerraCNAG-CRG, Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08028, Spain.
Vincent LoubiereInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Giorgio Lucio PapadopoulosInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Juan-Carlos Rivera-MuliaDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Lauriane FritschInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Pauline BouretUnit of Chromosomal Genetics and Chromostem Research Platform, CHU, Montpellier, France.
David CastilloCNAG-CRG, Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08028, Spain.
Josep Ll GelpiBarcelona Supercomputing Center, Barcelona, Spain; Department of Biochemistry and Molecular Biomedicine, University of Barcelona, Barcelona, Spain.
Modesto OrozcoDepartment of Biochemistry and Molecular Biomedicine, University of Barcelona, Barcelona, Spain; Institute for Research in Biomedicine, the Barcelona Institute of Science and Technology, Barcelona, Spain.
Cedric VaillantLaboratoire de Physique (UMR CNRS 5672), ENS de Lyon, Lyon, France.
Franck PellestorInstitute for Regenerative Medicine and Biotherapy, Univ Montpellier, INSERM UMR1183, F-34295 Montpellier, France; Unit of Chromosomal Genetics and Chromostem Research Platform, CHU, Montpellier, France.
Frederic BantigniesInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Marc A Marti-RenomCNAG-CRG, Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08028, Spain; Centre for Genomic Regulation, The Barcelona Institute for Science and Technology, Carrer del Doctor Aiguader 88, Barcelona 08003, Spain; Pompeu Fabra University, Doctor Aiguader 88, Barcelona 08003, Spain; CREA, PgLluís Companys 23, 08010 Barcelona, Spain.
David M GilbertDepartment of Biological Science and Center for Genomics and Personalized Medicine, Florida State University, Tallahassee, FL 32306, USA.
Jean-Marc LemaitreInstitute for Regenerative Medicine and Biotherapy, Univ Montpellier, INSERM UMR1183, F-34295 Montpellier, France; CHRU de Montpellier, Montpellier, France. Electronic address: jean-marc.lemaitre@inserm.fr.
Giacomo CavalliInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France. Electronic address: giacomo.cavalli@igh.cnrs.fr.
Université de Montpellier · FRCentre for Genomic Regulation · ESCentre National de la Recherche Scientifique · FRInstitut de Génétique Humaine · FRBarcelona Supercomputing Center · ESCentre Hospitalier Universitaire de Montpellier · FRFlorida State University · USInserm · FRInstitut polytechnique de Grenoble · FRUniversitat de Barcelona · ESUniversity of Minnesota Medical Center · US

Funding

Genome Plasticity during ES Cell Differentiation to Neural LineagesR01GM083337 · NIGMS · SAN DIEGO BIOMEDICAL RESEARCH INSTITUTE · PI David M Gilbert · 2007 to 2026
$6.1M
NIGMS NIH HHS R01 GM083337
6 · The paper itself

Abstract

To understand the role of the extensive senescence-associated 3D genome reorganization, we generated genome-wide chromatin interaction maps, epigenome, replication-timing, whole-genome bisulfite sequencing, and gene expression profiles from cells entering replicative senescence (RS) or upon oncogene-induced senescence (OIS). We identify senescence-associated heterochromatin domains (SAHDs). Differential intra- versus inter-SAHD interactions lead to the formation of senescence-associated heterochromatin foci (SAHFs) in OIS but not in RS. This OIS-specific configuration brings active genes located in genomic regions adjacent to SAHDs in close spatial proximity and favors their expression. We also identify DNMT1 as a factor that induces SAHFs by promoting HMGA2 expression. Upon DNMT1 depletion, OIS cells transition to a 3D genome conformation akin to that of cells in replicative senescence. These data show how multi-omics and imaging can identify critical features of RS and OIS and discover determinants of acute senescence and SAHF formation.

Indexed as

Genome, HumanOncogenesCells, CulturedCellular SenescenceChromatin Assembly and DisassemblyDNA (Cytosine-5-)-Methyltransferase 1DNA MethylationFibroblastsHeterochromatinHumansIn Situ Hybridization, FluorescenceDNA (Cytosine-5-)-Methyltransferase 1DNMT1 protein, humanHeterochromatin3D genome architecturechromatin compartmentsDNMT1gene regulationHi-Concogene-induced senescencereplicative senescencesenescence

Identifiers

PMID32220303
PMCPMC7208559
OpenAlexW3013543222

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.