Evidence map›Paper›PMID 27613868›Full record

ArticleThe Journal of biological chemistry2016

The Oncogenic Fusion Proteins SET-Nup214 and Sequestosome-1 (SQSTM1)-Nup214 Form Dynamic Nuclear Bodies and Differentially Affect Nuclear Protein and Poly(A)+ RNA Export.

Sarah A Port, Adélia Mendes, Christina Valkova, Christiane Spillner, Birthe Fahrenkrog, Christoph Kaether, Ralph H Kehlenbach

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Sarah A PortFrom the Department of Molecular Biology, Faculty of Medicine and the Göttingen Center for Molecular Biosciences (GZMB), Georg August University, Göttingen, Humboldtallee 23, 37073 Göttingen, Germany.
Adélia Mendesthe Institute of Molecular Biology and Medicine, Université Libre de Bruxelles, 6041 Charleroi, Belgium, and.
Christina Valkovathe Leibniz Institute on Aging,Fritz Lipmann Institute, Beutenbergstrasse 11, 07745 Jena, Germany.
Christiane SpillnerFrom the Department of Molecular Biology, Faculty of Medicine and the Göttingen Center for Molecular Biosciences (GZMB), Georg August University, Göttingen, Humboldtallee 23, 37073 Göttingen, Germany.
Birthe Fahrenkrogthe Institute of Molecular Biology and Medicine, Université Libre de Bruxelles, 6041 Charleroi, Belgium, and.
Christoph Kaetherthe Leibniz Institute on Aging,Fritz Lipmann Institute, Beutenbergstrasse 11, 07745 Jena, Germany.
Ralph H KehlenbachFrom the Department of Molecular Biology, Faculty of Medicine and the Göttingen Center for Molecular Biosciences (GZMB), Georg August University, Göttingen, Humboldtallee 23, 37073 Göttingen, Germany, rkehlen@gwdg.de.
University of Göttingen · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic rearrangements are a hallmark of several forms of leukemia and can lead to oncogenic fusion proteins. One example of an affected chromosomal region is the gene coding for Nup214, a nucleoporin that localizes to the cytoplasmic side of the nuclear pore complex (NPC). We investigated two such fusion proteins, SET-Nup214 and SQSTM1 (sequestosome)-Nup214, both containing C-terminal portions of Nup214. SET-Nup214 nuclear bodies containing the nuclear export receptor CRM1 were observed in the leukemia cell lines LOUCY and MEGAL. Overexpression of SET-Nup214 in HeLa cells leads to the formation of similar nuclear bodies that recruit CRM1, export cargo proteins, and certain nucleoporins and concomitantly affect nuclear protein and poly(A)

Indexed as

Active Transport, Cell NucleusDNA-Binding ProteinsExportin 1 ProteinHistone ChaperonesHumansIntranuclear Inclusion BodiesKaryopherinsNuclear Pore Complex ProteinsNuclear ProteinsPoly AReceptors, Cytoplasmic and NuclearRNA, MessengerSequestosome-1 ProteinTranscription FactorsDNA-Binding ProteinsExportin 1 ProteinHistone ChaperonesKaryopherinsNuclear Pore Complex ProteinsNuclear ProteinsNUP214 protein, humanPoly AReceptors, Cytoplasmic and NuclearRNA, MessengerSequestosome-1 ProteinSET protein, humanSQSTM1 protein, humanTranscription FactorsCRM1leukemiamRNAnuclear porenuclear transportnucleusNup214p62 (sequestosome-1 (SQSTM1))SET

Identifiers

PMID27613868
PMCPMC5087727
OpenAlexW2512195110

What OpenQuestion holds

Textmetadata
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.