Evidence map›Paper›PMID 28617241›Full record

ArticleeLife2017

Full length RTN3 regulates turnover of tubular endoplasmic reticulum via selective autophagy.

Paolo Grumati, Giulio Morozzi, Soraya Hölper, Muriel Mari, Marie-Lena I E Harwardt, Riqiang Yan, Stefan Müller, Fulvio Reggiori, Mike Heilemann, Ivan Dikic

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 276 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
276citing papers in PubMed, 4 pooled it
25.7field-weighted citation impact, top 1% 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

276 citing papers in PubMed, 4 syntheses or guidelines pooled it, 427 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Pooled it
  5. Emerging mechanisms of ATG8-independent non-canonical autophagy.Journal of physiology and biochemistry · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Selective autophagy in kidney health and disease.Nature reviews. Nephrology · 2026
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Metabolic Imaging and Molecular Signatures Reveal Metabolic Phenotypes in Recurrent Glioblastoma.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  18. Article
  19. TBK1 restricts IRGQ-mediated autophagy.Nature communications · 2026
    Article
  20. Review

216 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 4 countries.

Paolo GrumatiInstitute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.
Giulio MorozziInstitute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.
Soraya HölperInstitute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.
Muriel MariDepartment of Cell Biology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Marie-Lena I E HarwardtInstitute of Physical and Theoretical Chemistry, Goethe University Frankfurt, Frankfurt, Germany.
Riqiang YanDepartment of Neurosciences, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, United States.
Stefan MüllerInstitute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.
Fulvio ReggioriDepartment of Cell Biology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Mike HeilemannInstitute of Physical and Theoretical Chemistry, Goethe University Frankfurt, Frankfurt, Germany.
Ivan DikicInstitute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.ORCID http://orcid.org/0000-0001-8156-9511
Goethe University Frankfurt · DEUniversity Medical Center Groningen · NLCleveland Clinic · US

Funding

Roles of reticulon proteins in neurodegenerative disordersR01AG025493 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI YAN, RIQIANG · 2005 to 2024
$5.9M
NIA NIH HHS R01 AG025493
6 · The paper itself

Abstract

The turnover of endoplasmic reticulum (ER) ensures the correct biological activity of its distinct domains. In mammalian cells, the ER is degraded via a selective autophagy pathway (ER-phagy), mediated by two specific receptors: FAM134B, responsible for the turnover of ER sheets and SEC62 that regulates ER recovery following stress. Here, we identified reticulon 3 (RTN3) as a specific receptor for the degradation of ER tubules. Oligomerization of the long isoform of RTN3 is sufficient to trigger fragmentation of ER tubules. The long N-terminal region of RTN3 contains several newly identified LC3-interacting regions (LIR). Binding to LC3s/GABARAPs is essential for the fragmentation of ER tubules and their delivery to lysosomes. RTN3-mediated ER-phagy requires conventional autophagy components, but is independent of FAM134B. None of the other reticulon family members have the ability to induce fragmentation of ER tubules during starvation. Therefore, we assign a unique function to RTN3 during autophagy.

Indexed as

AutophagyCarrier ProteinsCell LineEndoplasmic ReticulumHumansMembrane ProteinsNerve Tissue ProteinsProtein MultimerizationCarrier ProteinsMembrane ProteinsNerve Tissue ProteinsRTN3 protein, humanautophagybiochemistrycell biologyendoplasmic reticulumnonereticulonRTN3selective autophagy

Identifiers

PMID28617241
PMCPMC5517149
OpenAlexW2625879429

What OpenQuestion holds

Textmetadata
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.