Evidence map›Paper›PMID 28504640›Full record

ArticleeLife2017

The Sec61 translocon limits IRE1α signaling during the unfolded protein response.

Arunkumar Sundaram, Rachel Plumb, Suhila Appathurai, Malaiyalam Mariappan

Open 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. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.8field-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

41 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. ER CaCell & bioscience · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. UPRFrontiers in cell and developmental biology · 2022
    Review
  20. Review
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 2 institutions in 2 countries.

Arunkumar SundaramDepartment of Cell Biology, Nanobiology Institute, Yale School of Medicine, West Haven, United States.
Rachel PlumbDepartment of Cell Biology, Nanobiology Institute, Yale School of Medicine, West Haven, United States.ORCID 0000-0001-5329-5947
Suhila AppathuraiDepartment of Cell Biology, Nanobiology Institute, Yale School of Medicine, West Haven, United States.
Malaiyalam MariappanDepartment of Cell Biology, Nanobiology Institute, Yale School of Medicine, West Haven, United States.ORCID 0000-0002-2966-1182
Yale University · USUniversiti Sains Malaysia · MY

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
The mechanism of Ire1-mediated mRNA cleavage during endoplasmic reticulum stressR01GM117386 · NIGMS · YALE UNIVERSITY · PI MARIAPPAN, MALAIYALAM · 2016 to 2024
$3.0M
NIGMS NIH HHS R01 GM117386NIGMS NIH HHS T32 GM007223
6 · The paper itself

Abstract

IRE1α is an endoplasmic reticulum (ER) localized endonuclease activated by misfolded proteins in the ER. Previously, we demonstrated that IRE1α forms a complex with the Sec61 translocon, to which its substrate XBP1u mRNA is recruited for cleavage during ER stress (Plumb et al., 2015). Here, we probe IRE1α complexes in cells with blue native PAGE immunoblotting. We find that IRE1α forms a hetero-oligomeric complex with the Sec61 translocon that is activated upon ER stress with little change in the complex. In addition, IRE1α oligomerization, activation, and inactivation during ER stress are regulated by Sec61. Loss of the IRE1α-Sec61 translocon interaction as well as severe ER stress conditions causes IRE1α to form higher-order oligomers that exhibit continuous activation and extended cleavage of XBP1u mRNA. Thus, we propose that the Sec61-IRE1α complex defines the extent of IRE1α activity and may determine cell fate decisions during ER stress conditions.

Indexed as

Signal TransductionUnfolded Protein ResponseEndoribonucleasesHEK293 CellsHumansImmunoblottingProtein BindingProtein MultimerizationProtein Serine-Threonine KinasesSEC Translocation ChannelsEndoribonucleasesERN1 protein, humanProtein Serine-Threonine KinasesSEC Translocation Channelscell biologyendoplasmic reticulumER stressnoneunfolded protein response

Identifiers

PMID28504640
PMCPMC5449187
OpenAlexW2615836287

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.