Evidence map›Paper›PMID 29887377›Full record

ArticleCell2018

Higher-Order Inter-chromosomal Hubs Shape 3D Genome Organization in the Nucleus.

Sofia A Quinodoz, Noah Ollikainen, Barbara Tabak, Ali Palla, Jan Marten Schmidt, Elizabeth Detmar, Mason M Lai, Alexander A Shishkin, Prashant Bhat, Yodai Takei and 10 more

Abstract read
In one paragraph

Article in Cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 544 papers.

0numbers the graph read from it
0cells of the map it votes in
544citing papers in PubMed
–field-weighted citation impact
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

544 citing papers in PubMed.

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  18. CAD-C: An engineered nuclease enables repair-freebioRxiv : the preprint server for biology · 2026
    Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Sofia A QuinodozDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Noah OllikainenDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Barbara TabakProgram in Bioinformatics and Integrative Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Ali PallaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Jan Marten SchmidtDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Elizabeth DetmarDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Mason M LaiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Alexander A ShishkinDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Prashant BhatDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Yodai TakeiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Vickie TrinhDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Erik AznauryanDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Pamela RussellDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO 80045, USA.
Christine ChengDepartment of Biology, Boston University, Boston, MA 02215, USA.
Marko JovanovicDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Amy ChowDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Long CaiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Patrick McDonelProgram in Bioinformatics and Integrative Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Manuel GarberProgram in Bioinformatics and Integrative Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Mitchell GuttmanDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: mguttman@caltech.edu.

Funding

UCLA-Caltech Medical Scientist Training ProgramT32GM008042 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AJIJOLA, OLUJIMI A, DAWSON, DAVID WAYNE · 1985 to 2023
$29.9M
Rules of gene expression modeled on human dendritic cell response to pathogensU01HG007910 · NHGRI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GARBER, MANUEL, LUBAN, JEREMY · 2015 to 2017
$6.1M
Deciphering the function and mechanisms of lncRNA-mediated organization of nuclear compartmentsU01DA040612 · NIDA · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI GUTTMAN, MITCHELL, RINN, JOHN LOUIS · 2015 to 2019
$4.1M
Novel tools to comprehensively map dynamic organization of RNA and DNA in higher-order nuclear structures within single cellsU01HL130007 · NHLBI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI GUTTMAN, MITCHELL, ISMAGILOV, RUSTEM F · 2015 to 2019
$3.9M
Howard Hughes Medical InstituteNHGRI NIH HHS U01 HG007910NHLBI NIH HHS U01 HL130007NIDA NIH HHS U01 DA040612NIGMS NIH HHS T32 GM008042
6 · The paper itself

Abstract

Eukaryotic genomes are packaged into a 3-dimensional structure in the nucleus. Current methods for studying genome-wide structure are based on proximity ligation. However, this approach can fail to detect known structures, such as interactions with nuclear bodies, because these DNA regions can be too far apart to directly ligate. Accordingly, our overall understanding of genome organization remains incomplete. Here, we develop split-pool recognition of interactions by tag extension (SPRITE), a method that enables genome-wide detection of higher-order interactions within the nucleus. Using SPRITE, we recapitulate known structures identified by proximity ligation and identify additional interactions occurring across larger distances, including two hubs of inter-chromosomal interactions that are arranged around the nucleolus and nuclear speckles. We show that a substantial fraction of the genome exhibits preferential organization relative to these nuclear bodies. Our results generate a global model whereby nuclear bodies act as inter-chromosomal hubs that shape the overall packaging of DNA in the nucleus.

Indexed as

Cell NucleolusCell NucleusChromosome MappingChromosomesDNAEukaryotaGenomeHumansStructure-Activity RelationshipDNAgenome structurehigher-order nuclear structuremulti-way interactionsnuclear organizationnuclear speckleNuclear structurenucleolusRNA DNA interactionsSPRITE

Identifiers

PMID29887377
PMCPMC6548320

What OpenQuestion holds

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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.