Evidence map›Paper›PMID 26082182›Full record

ReviewCellular and molecular life sciences : CMLS2015

Mechanisms for exporting large-sized cargoes from the endoplasmic reticulum.

Kota Saito, Toshiaki Katada

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Nlp-dependent ER-to-Golgi transport.International journal of biological sciences · 2024
    Article
  2. Article
  3. Collagen VII maintains proteostasis in dermal fibroblasts by scaffolding TANGO1 cargo.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. The enigmatic ATP supply of the endoplasmic reticulum.Biological reviews of the Cambridge Philosophical Society · 2019
    Review
  9. Article
  10. Models of Intracellular Transport: Pros and Cons.Frontiers in cell and developmental biology · 2019
    Article
  11. Collagen I: a kingpin for rotator cuff tendon pathology.American journal of translational research · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Intracellular mechanisms of molecular recognition and sorting for transport of large extracellular matrix molecules.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  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

2 authors.

Kota SaitoDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan. ksaito@mol.f.u-tokyo.ac.jp.
Toshiaki KatadaDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cargo proteins exported from the endoplasmic reticulum to the Golgi apparatus are typically transported in coat protein complex II (COPII)-coated vesicles of 60-90 nm diameter. Several cargo molecules including collagens and chylomicrons form structures that are too large to be accommodated by these vesicles, but their secretion still requires COPII proteins. Here, we first review recent progress on large cargo secretions derived especially from animal models and human diseases, which indicate the importance of COPII proteins. We then discuss the recent isolation of specialized factors that modulate the process of COPII-dependent cargo formation to facilitate the exit of large-sized cargoes from the endoplasmic reticulum. Based on these findings, we propose a model that describes the importance of the GTPase cycle for secretion of oversized cargoes. Next, we summarize reports that describe the structures of COPII proteins and how these results provide insight into the mechanism of assembly of the large cargo carriers. Finally, we discuss what issues remain to be solved in the future.

Indexed as

Models, BiologicalAnimalsAntigens, NeoplasmAryl Hydrocarbon Receptor Nuclear TranslocatorCarrier ProteinsChylomicronsCollagenCOP-Coated VesiclesEndoplasmic ReticulumGolgi ApparatusGTP PhosphohydrolasesHumansNeoplasm ProteinsProtein TransportAntigens, NeoplasmARNT protein, humanAryl Hydrocarbon Receptor Nuclear TranslocatorCarrier ProteinsChylomicronsCollagenGTP PhosphohydrolasesMIA2 protein, humanNeoplasm ProteinsChylomicronCollagenCOPIIcTAGE5TANGO1

Identifiers

PMID26082182
PMCPMC4565863

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.