Evidence map›Paper›PMID 32579423›Full record

ArticleMolecular biology of the cell2020

Nuclear body phase separation drives telomere clustering in ALT cancer cells.

Huaiying Zhang, Rongwei Zhao, Jason Tones, Michel Liu, Robert L Dilley, David M Chenoweth, Roger A Greenberg, Michael A Lampson

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology of the cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

93 citing papers in PubMed, 118 citations in OpenAlex.

  1. Kinetic Control of Condensate Function: How the Formation Dynamics of APBs Influence ALT Cancer Telomere Length Heterogeneity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
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33 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Huaiying ZhangDepartments of Biology, University of Pennsylvania, Philadelphia, PA 19104.
Rongwei ZhaoDepartments of Chemistry, University of Pennsylvania, Philadelphia, PA 19104.
Jason TonesDepartments of Chemistry, University of Pennsylvania, Philadelphia, PA 19104.
Michel LiuDepartments of Biology, University of Pennsylvania, Philadelphia, PA 19104.
Robert L DilleyPenn Center for Genome Integrity, University of Pennsylvania, Philadelphia, PA 19104.
David M ChenowethDepartment of Cancer Biology, Basser Center for BRCA, Perelman School of Medicine.
Roger A GreenbergPenn Center for Genome Integrity, University of Pennsylvania, Philadelphia, PA 19104.
Michael A LampsonPenn Center for Genome Integrity, University of Pennsylvania, Philadelphia, PA 19104.
University of Pennsylvania · USPenn Center for AIDS Research · US

Funding

PSOC@Penn Education and OutreachU54CA193417 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2015 to 2020
$10.5M
Roles of Chromatin Modification in BRCA1 Dependent DNA RepairR01CA174904 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Roger A Greenberg · 2013 to 2026
$4.8M
Cell Biological mechanisms of centromere driveR35GM122475 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Michael Lampson · 2017 to 2026
$4.5M
DNA Double Strand Break Chromatin Alterations and Genome IntegrityR01GM101149 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GREENBERG, ROGER A · 2013 to 2025
$4.0M
Targeting Nucleic Acid Junctions with Small MoleculesR01GM118510 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI CHENOWETH, DAVID MICHAEL · 2016 to 2020
$1.6M
Nuclear body assembly and function in telomerase-free cancer cellsK22CA237632 · NCI · CARNEGIE-MELLON UNIVERSITY · PI ZHANG, HUAIYING · 2019 to 2021
$498k
NCI NIH HHS K22 CA237632NCI NIH HHS R01 CA174904NCI NIH HHS U54 CA193417NIGMS NIH HHS R01 GM101149NIGMS NIH HHS R01 GM118510NIGMS NIH HHS R35 GM122475
6 · The paper itself

Abstract

Telomerase-free cancer cells employ a recombination-based alternative lengthening of telomeres (ALT) pathway that depends on ALT-associated promyelocytic leukemia nuclear bodies (APBs), whose function is unclear. We find that APBs behave as liquid condensates in response to telomere DNA damage, suggesting two potential functions: condensation to enrich DNA repair factors and coalescence to cluster telomeres. To test these models, we developed a chemically induced dimerization approach to induce de novo APB condensation in live cells without DNA damage. We show that telomere-binding protein sumoylation nucleates APB condensation via interactions between small ubiquitin-like modifier (SUMO) and SUMO interaction motif (SIM), and that APB coalescence drives telomere clustering. The induced APBs lack DNA repair factors, indicating that APB functions in promoting telomere clustering can be uncoupled from enriching DNA repair factors. Indeed, telomere clustering relies only on liquid properties of the condensate, as an alternative condensation chemistry also induces clustering independent of sumoylation. Our findings introduce a chemical dimerization approach to manipulate phase separation and demonstrate how the material properties and chemical composition of APBs independently contribute to ALT, suggesting a general framework for how chromatin condensates promote cellular functions.

Indexed as

Cell LineDNA DamageDNA RepairHumansLeukemia, Promyelocytic, AcuteNuclear ProteinsPromyelocytic Leukemia ProteinTelomeraseTelomereTelomere HomeostasisTelomeric Repeat Binding Protein 1Transcription FactorsNuclear ProteinsPromyelocytic Leukemia ProteinTelomeraseTelomeric Repeat Binding Protein 1Transcription Factors

Identifiers

PMID32579423
PMCPMC7543070
OpenAlexW3037582659

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.