Evidence map›Paper›PMID 21847093›Full record

ArticleThe EMBO journal2011

ERK7 is a negative regulator of protein secretion in response to amino-acid starvation by modulating Sec16 membrane association.

Margarita Zacharogianni, Vangelis Kondylis, Yang Tang, Hesso Farhan, Despina Xanthakis, Florian Fuchs, Michael Boutros, Catherine Rabouille

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

69 citing papers in PubMed, 115 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. ER exit in physiology and disease.Frontiers in molecular biosciences · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Sorting and Export of Proteins at the Endoplasmic Reticulum.Cold Spring Harbor perspectives in biology · 2023
    Review
  15. Review
  16. Review
  17. Life (Basel, Switzerland) · 2022
    Article
  18. ER exit sites take the strain.The EMBO journal · 2022
    Article
  19. Article
  20. Article

9 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 5 institutions in 3 countries.

Margarita ZacharogianniDepartment of Cell Biology, Cell microscopy Centre, UMC Utrecht, Heidelberglaan, The Netherlands.
Vangelis Kondylis
Yang Tang
Hesso Farhan
Despina Xanthakis
Florian Fuchs
Michael Boutros
Catherine Rabouille
University Medical Center Utrecht · NLBiotechnology Institute Thurgau · CHHeidelberg University · DEHubrecht Institute for Developmental Biology and Stem Cell Research · NLUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNAi screening for kinases regulating the functional organization of the early secretory pathway in Drosophila S2 cells has identified the atypical Mitotic-Associated Protein Kinase (MAPK) Extracellularly regulated kinase 7 (ERK7) as a new modulator. We found that ERK7 negatively regulates secretion in response to serum and amino-acid starvation, in both Drosophila and human cells. Under these conditions, ERK7 turnover through the proteasome is inhibited, and the resulting higher levels of this kinase lead to a modification in a site within the C-terminus of Sec16, a key ER exit site component. This post-translational modification elicits the cytoplasmic dispersion of Sec16 and the consequent disassembly of the ER exit sites, which in turn results in protein secretion inhibition. We found that ER exit site disassembly upon starvation is TOR complex 1 (TORC1) independent, showing that under nutrient stress conditions, cell growth is not only inhibited at the transcriptional and translational levels, but also independently at the level of secretion by inhibiting the membrane flow through the early secretory pathway. These results reveal the existence of new signalling circuits participating in the complex regulation of cell growth.

Indexed as

Gene Expression RegulationAnimalsCell LineDrosophilaDrosophila ProteinsExtracellular Signal-Regulated MAP KinasesMicroscopy, FluorescenceMicroscopy, ImmunoelectronProteinsVesicular Transport ProteinsDrosophila ProteinsExtracellular Signal-Regulated MAP KinasesProteinsSec16 protein, DrosophilaVesicular Transport Proteins

Identifiers

PMID21847093
PMCPMC3173787
OpenAlexW1807950231

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.