Evidence map›Paper›PMID 27872256›Full record

ArticleThe Journal of cell biology2016

The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR.

Sandra Scharaw, Murat Iskar, Alessandro Ori, Gaelle Boncompain, Vibor Laketa, Ina Poser, Emma Lundberg, Franck Perez, Martin Beck, Peer Bork and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Tyrosine Kinase Receptors in Oncology.International journal of molecular sciences · 2020
    Review
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  19. The Functional Role of SEC23 in Vesicle Transportation, Autophagy and Cancer.International journal of biological sciences · 2019
    Review
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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

11 authors at 5 institutions in 3 countries.

Sandra ScharawCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.ORCID http://orcid.org/0000-0001-9428-3213
Murat IskarStructural and Computational Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.ORCID http://orcid.org/0000-0001-8603-4313
Alessandro OriStructural and Computational Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.ORCID http://orcid.org/0000-0002-3046-0871
Gaelle BoncompainInstitut Curie, Paris Sciences et Lettres Research University, 75248 Paris, France.
Vibor LaketaCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Ina PoserMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Emma LundbergScience for Life Laboratory, KTH Royal Institute of Technology, 17121 Solna, Sweden.ORCID http://orcid.org/0000-0001-7034-0850
Franck PerezInstitut Curie, Paris Sciences et Lettres Research University, 75248 Paris, France.ORCID http://orcid.org/0000-0002-9129-9401
Martin BeckStructural and Computational Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Peer BorkStructural and Computational Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Rainer PepperkokCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany pepperko@embl.de.ORCID http://orcid.org/0000-0002-9762-3583
European Molecular Biology Laboratory · DEUniversité Paris Sciences et Lettres · FRMax Delbrück Center · DEMax Planck Institute of Molecular Cell Biology and Genetics · DEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stimulation of cells with epidermal growth factor (EGF) induces internalization and partial degradation of the EGF receptor (EGFR) by the endo-lysosomal pathway. For continuous cell functioning, EGFR plasma membrane levels are maintained by transporting newly synthesized EGFRs to the cell surface. The regulation of this process is largely unknown. In this study, we find that EGF stimulation specifically increases the transport efficiency of newly synthesized EGFRs from the endoplasmic reticulum to the plasma membrane. This coincides with an up-regulation of the inner coat protein complex II (COPII) components SEC23B, SEC24B, and SEC24D, which we show to be specifically required for EGFR transport. Up-regulation of these COPII components requires the transcriptional regulator RNF11, which localizes to early endosomes and appears additionally in the cell nucleus upon continuous EGF stimulation. Collectively, our work identifies a new regulatory mechanism that integrates the degradation and transport of EGFR in order to maintain its physiological levels at the plasma membrane.

Indexed as

ProteolysisTranscription, GeneticCarrier ProteinsCell MembraneCell NucleusCOP-Coated VesiclesDNA-Binding ProteinsEndosomesEpidermal Growth FactorErbB ReceptorsGolgi ApparatusGreen Fluorescent ProteinsHeLa CellsHumansPhosphatidylinositol 3-KinasesProtein TransportCarrier ProteinsDNA-Binding Proteinsenhanced green fluorescent proteinEpidermal Growth FactorErbB ReceptorsGreen Fluorescent ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNF11 protein, human

Identifiers

PMID27872256
PMCPMC5119934
OpenAlexW2554732389

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Registered trials

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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.