Evidence map›Paper›PMID 26833788›Full record

ArticleThe Journal of cell biology2016

Distinct requirements for intra-ER sorting and budding of peroxisomal membrane proteins from the ER.

Gaurav Agrawal, Scott N Fassas, Zhi-Jie Xia, Suresh Subramani

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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Synthetic and systems biotechnology · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Peroxisomal Membrane Contact Sites in Yeasts.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Lipid Droplet and Peroxisome Biogenesis: Do They Go Hand-in-Hand?Frontiers in cell and developmental biology · 2019
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Unloosing the Gordian knot of peroxisome formation.Current opinion in cell biology · 2018
    Review
  18. Review
  19. Review
  20. Article
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

4 authors at 1 institution in 1 country.

Gaurav AgrawalSection of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Scott N FassasSection of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Zhi-Jie XiaSection of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Suresh SubramaniSection of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093 ssubramani@ucsd.edu.
University of California, San Diego · US

Funding

TARGETING OF PROTEINS INTO PEROXISOMESR01DK041737 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AITCHISON, JOHN D., SUBRAMANI, SURESH · 1990 to 2025
$8.4M
NIDDK NIH HHS R01 DK041737NIDDK NIH HHS R01DK41737
6 · The paper itself

Abstract

During de novo peroxisome biogenesis, importomer complex proteins sort via two preperoxisomal vesicles (ppVs). However, the sorting mechanisms segregating peroxisomal membrane proteins to the preperoxisomal endoplasmic reticulum (pER) and into ppVs are unknown. We report novel roles for Pex3 and Pex19 in intra-endoplasmic reticulum (ER) sorting and budding of the RING-domain peroxins (Pex2, Pex10, and Pex12). Pex19 bridged the interaction at the ER between Pex3 and RING-domain proteins, resulting in a ternary complex that was critical for the intra-ER sorting and subsequent budding of the RING-domain peroxins. Although the docking subcomplex proteins (Pex13, Pex14, and Pex17) also required Pex19 for budding from the ER, they sorted to the pER independently of Pex3 and Pex19 and were spatially segregated from the RING-domain proteins. We also discovered a unique role for Pex3 in sorting Pex10 and Pex12, but with the docking subcomplex. Our study describes an intra-ER sorting process that regulates segregation, packaging, and budding of peroxisomal importomer subcomplexes, thereby preventing their premature assembly at the ER.

Indexed as

Endoplasmic ReticulumFungal ProteinsMembrane ProteinsMultiprotein ComplexesPeroxisomesPichiaProtein BindingProtein Interaction Domains and MotifsProtein TransportTime FactorsFungal ProteinsMembrane ProteinsMultiprotein Complexes

Identifiers

PMID26833788
PMCPMC4748575
OpenAlexW2267784944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.