Evidence map›Paper›PMID 31131328›Full record

ArticleScience advances2019

ARID1A spatially partitions interphase chromosomes.

Shuai Wu, Nail Fatkhutdinov, Leah Rosin, Jennifer M Luppino, Osamu Iwasaki, Hideki Tanizawa, Hsin-Yao Tang, Andrew V Kossenkov, Alessandro Gardini, Ken-Ichi Noma and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

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  16. mNature cell biology · 2021
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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 2 institutions in 2 countries.

Shuai WuGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0002-3183-5081
Nail FatkhutdinovGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0003-3152-9321
Leah RosinDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-2489-4016
Jennifer M LuppinoDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-2078-7619
Osamu IwasakiGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Hideki TanizawaGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0002-2573-2473
Hsin-Yao TangProteomics and Metabolomics Facility, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0003-1838-018X
Andrew V KossenkovCenter for Systems and Computational Biology, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0002-1536-0418
Alessandro GardiniGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Ken-Ichi NomaGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.
David W SpeicherCenter for Systems and Computational Biology, The Wistar Institute, Philadelphia, PA 19104, USA.
Eric F JoyceDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Rugang ZhangGene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104, USA.ORCID 0000-0002-7255-2360
The Wistar Institute · USUniversity of Pennsylvania · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
STRUCTURAL BASIS FOR EPIGENETICS IN AGING AND LONGEVITYP01AG031862 · NIA · WISTAR INSTITUTE · PI GARCIA, BENJAMIN A · 2008 to 2022
$28.3M
SPORE in Ovarian CancerP50CA228991 · NCI · JOHNS HOPKINS UNIVERSITY · PI Tian-Li Wang · 2018 to 2026
$20.5M
Regulation of chromatin folding in space and timeR35GM128903 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Eric F. Joyce · 2018 to 2026
$4.2M
Mechanistic basis and therapeutic strategies for ARID1A mutation in ovarian cancerR01CA202919 · NCI · WISTAR INSTITUTE · PI Xi Chen, Rugang Zhang · 2016 to 2026
$4.1M
Identification of Ovarian Cancer Plasma BiomarkersR01CA131582 · NCI · WISTAR INSTITUTE · PI SPEICHER, DAVID W. · 2009 to 2018
$4.1M
Role of BRCA1 Pathway in Regulating Oncogene-Induced SenescenceR01CA160331 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2012 to 2021
$4.0M
Targeting EZH2 in CARM1-expressing epithelial ovarian cancerR01CA163377 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2012 to 2021
$3.7M
Synthetic lethality based combination approaches to ARID1A mutation in ovarian cancerR01CA239128 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2019 to 2024
$2.5M
Advancing Cancer Research through Comprehensive Proteomics and Metabolomics AnalysesR50CA221838 · NCI · WISTAR INSTITUTE · PI Hsin-Yao Tang · 2017 to 2026
$2.1M
Condensin connects 3D genome organization, chromosomal segregation, andgene regulation via its interactions with transcription-related factors.R01GM124195 · NIGMS · WISTAR INSTITUTE · PI NOMA, KENICHI · 2017 to 2020
$1.8M
Integrative Approach to Comprehensive Analysis of High Throughput Data on a Cancer Center LevelR50CA211199 · NCI · WISTAR INSTITUTE · PI Andrew V Kossenkov · 2016 to 2026
$1.6M
NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA228991NCI NIH HHS R01 CA131582NCI NIH HHS R01 CA160331NCI NIH HHS R01 CA163377NCI NIH HHS R01 CA202919NCI NIH HHS R01 CA239128NCI NIH HHS R50 CA211199NCI NIH HHS R50 CA221838NIA NIH HHS P01 AG031862NIGMS NIH HHS R01 GM124195NIGMS NIH HHS R35 GM128903
6 · The paper itself

Abstract

ARID1A, a subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin-remodeling complex, localizes to both promoters and enhancers to influence transcription. However, the role of ARID1A in higher-order spatial chromosome partitioning and genome organization is unknown. Here, we show that ARID1A spatially partitions interphase chromosomes and regulates higher-order genome organization. The SWI/SNF complex interacts with condensin II, and they display significant colocalizations at enhancers. ARID1A knockout drives the redistribution of condensin II preferentially at enhancers, which positively correlates with changes in transcription. ARID1A and condensin II contribute to transcriptionally inactive B-compartment formation, while ARID1A weakens the border strength of topologically associated domains. Condensin II redistribution induced by ARID1A knockout positively correlates with chromosome sizes, which negatively correlates with interchromosomal interactions. ARID1A loss increases the trans interactions of small chromosomes, which was validated by three-dimensional interphase chromosome painting. These results demonstrate that ARID1A is important for large-scale genome folding and spatially partitions interphase chromosomes.

Indexed as

Adenosine TriphosphatasesBinding SitesCell Line, TumorChromatinChromosomesCluster AnalysisDNA-Binding ProteinsEnhancer Elements, GeneticGene Expression ProfilingHumansInterphaseMultiprotein ComplexesPromoter Regions, GeneticProtein BindingRNA-SeqSerine EndopeptidasesAdenosine TriphosphatasesARID1A protein, humanChromatincondensin complexesDNA-Binding ProteinsMultiprotein ComplexesPRSS27 protein, humanSerine EndopeptidasesTranscription Factors

Identifiers

PMID31131328
PMCPMC6531001
OpenAlexW2945248524

What OpenQuestion holds

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LicenceCC BY-NC
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.