Evidence map›Paper›PMID 27827373›Full record

ArticleNature communications2016

BMI1 regulates PRC1 architecture and activity through homo- and hetero-oligomerization.

Felicia Gray, Hyo Je Cho, Shirish Shukla, Shihan He, Ashley Harris, Bohdan Boytsov, Łukasz Jaremko, Mariusz Jaremko, Borries Demeler, Elizabeth R Lawlor and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
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  3. Polycomb-mediated 3D chromatin interactions in gene regulation.Current opinion in genetics & development · 2026
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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

12 authors at 5 institutions in 2 countries.

Felicia GrayDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Hyo Je ChoDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Shirish ShuklaDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Shihan HeDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Ashley HarrisTranslational Oncology Program, University of Michigan, Ann Arbor, Michigan 48109, USA.
Bohdan BoytsovDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Łukasz JaremkoDeutsches Zentrum fur Neurodegenerative Erkrankungen (DZNE), Am Fassberg 11, 37077 Goettingen, Germany.
Mariusz JaremkoMax-Planck Institute of Biophysical Chemistry, NMR-based Department for Structural Biology, Am Fassberg 11, 37077 Goettingen, Germany.
Borries DemelerDepartment of Biochemistry, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, USA.
Elizabeth R LawlorDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Jolanta GrembeckaDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Tomasz CierpickiDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · USGerman Center for Neurodegenerative Diseases · DEMax Planck Institute for Biophysical Chemistry · DEThe University of Texas Health Science Center at San Antonio · US

Funding

Development of an UltraScan Meta-Scheduler for HPC Job SubmissionR01GM120600 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Emre H. Brookes, BORRIES DEMELER · 2016 to 2026
$3.6M
Development of novel anti-leukemia agents targeting the menin-MLL interactionR01CA160467 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GREMBECKA, JOLANTA · 2011 to 2021
$3.4M
Investigating Oncogenic Cooperation between BMI-1 and EWS-FLI1R01CA134604 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAWLOR, ELIZABETH R · 2010 to 2014
$1.5M
Targeting protein-protein interactions of Bmi1 oncoproteinR01CA201204 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GREMBECKA, JOLANTA · 2016 to 2018
$959k
Inhibition of CDC25B phosphatase by targeting protein-protein interactionsR01CA181185 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CIERPICKI, TOMASZ · 2014 to 2016
$952k
NCI NIH HHS R01 CA134604NCI NIH HHS R01 CA160467NCI NIH HHS R01 CA181185NCI NIH HHS R01 CA201204
6 · The paper itself

Abstract

BMI1 is a core component of the polycomb repressive complex 1 (PRC1) and emerging data support a role of BMI1 in cancer. The central domain of BMI1 is involved in protein-protein interactions and is essential for its oncogenic activity. Here, we present the structure of BMI1 bound to the polyhomeotic protein PHC2 illustrating that the central domain of BMI1 adopts an ubiquitin-like (UBL) fold and binds PHC2 in a β-hairpin conformation. Unexpectedly, we find that the UBL domain is involved in homo-oligomerization of BMI1. We demonstrate that both the interaction of BMI1 with polyhomeotic proteins and homo-oligomerization via UBL domain are necessary for H2A ubiquitination activity of PRC1 and for clonogenic potential of U2OS cells. Here, we also emphasize need for joint application of NMR spectroscopy and X-ray crystallography to determine the overall structure of the BMI1-PHC2 complex.

Indexed as

Protein MultimerizationCell Line, TumorCrystallography, X-RayHistonesHumansMagnetic Resonance SpectroscopyPolycomb Repressive Complex 1Polycomb Repressive Complex 2Protein DomainsProtein Structure, TertiaryUbiquitinationBMI1 protein, humanHistonesPHC2 protein, humanPolycomb Repressive Complex 1Polycomb Repressive Complex 2

Identifiers

PMID27827373
PMCPMC5105191
OpenAlexW2554647387

What OpenQuestion holds

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LicenceCC BY
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.