Evidence map›Paper›PMID 31792031›Full record

ArticleThe Journal of biological chemistry2020

PERK-mediated induction of microRNA-483 disrupts cellular ATP homeostasis during the unfolded protein response.

Nobuhiko Hiramatsu, Karen Chiang, Cathrine Aivati, Jeffrey J Rodvold, Ji-Min Lee, Jaeseok Han, Leon Chea, Maurizio Zanetti, Edward H Koo, Jonathan H Lin

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. ATF6 is essential for human cone photoreceptor development.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. The role of microRNAs in cell death pathways.Yeungnam University journal of medicine · 2021
    Article
  11. Article
  12. MicroRNA-494 Regulates Endoplasmic Reticulum Stress in Endothelial Cells.Frontiers in cell and developmental biology · 2021
    Article
  13. Review
  14. Frontiers in microbiology · 2020
    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

10 authors at 4 institutions in 3 countries.

Nobuhiko HiramatsuDepartment of Pathology, University of California San Diego, La Jolla, California 92093-0612.
Karen ChiangDepartment of Pathology, University of California San Diego, La Jolla, California 92093-0612; Department of Neurosciences, University of California San Diego, La Jolla, California 92093-0612.
Cathrine AivatiDepartment of Pathology, University of California San Diego, La Jolla, California 92093-0612.
Jeffrey J RodvoldMoores Cancer Center, University of California San Diego, La Jolla, California 92093-0612.
Ji-Min LeeSoonchunhyang Institute of Med-bio Science, Soonchunhyang University, Asan 31151, Korea.
Jaeseok HanSoonchunhyang Institute of Med-bio Science, Soonchunhyang University, Asan 31151, Korea.
Leon CheaDepartment of Pathology, Stanford University, Stanford, California 94304.
Maurizio ZanettiMoores Cancer Center, University of California San Diego, La Jolla, California 92093-0612.
Edward H KooDepartment of Neurosciences, University of California San Diego, La Jolla, California 92093-0612; Departments of Medicine and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, 117549 Singapore.
Jonathan H LinDepartment of Pathology, University of California San Diego, La Jolla, California 92093-0612; Department of Pathology, Stanford University, Stanford, California 94304; Veterans Affairs Palo Alto Healthcare System, Palo Alto, California 94304. Electronic address: jlinn@stanford.edu.
University of California, San Diego · USSoonchunhyang University · KRStanford University · USVA Palo Alto Health Care System · US

Funding

VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI David Mitchell Smith · 1994 to 2026
$78.4M
VIRUS-INDUCED BRAIN PATHOLOGYP50AG005131 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BREWER, JAMES B · 1985 to 2018
$55.4M
Protein Homeostasis and Proteotoxicity MechanismsR01NS088485 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LIN, JONATHAN · 2015 to 2024
$3.0M
Molecular Pathology of AchromatopsiaR01EY027335 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LIN, JONATHAN · 2017 to 2019
$1.2M
Cellular and Molecular Mechanisms of Age-Related Retinal DegenerationI01BX002284 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI LIN, JONATHAN · 2014 to 2023
–
Endoplasmic Reticulum Stress in NeurodegenerationI01RX002340 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI JONATHAN LIN · 2017 to 2026
–
BLRD VA I01 BX002284NEI NIH HHS R01 EY027335NIAID NIH HHS P30 AI036214NIA NIH HHS P50 AG005131NINDS NIH HHS R01 NS088485RRD VA I01 RX002340
6 · The paper itself

Abstract

Endoplasmic reticulum (ER) stress activates the unfolded protein response (UPR), which reduces levels of misfolded proteins. However, if ER homeostasis is not restored and the UPR remains chronically activated, cells undergo apoptosis. The UPR regulator, PKR-like endoplasmic reticulum kinase (PERK), plays an important role in promoting cell death when persistently activated; however, the underlying mechanisms are poorly understood. Here, we profiled the microRNA (miRNA) transcriptome in human cells exposed to ER stress and identified miRNAs that are selectively induced by PERK signaling. We found that expression of a PERK-induced miRNA, miR-483, promotes apoptosis in human cells. miR-483 induction was mediated by a transcription factor downstream of PERK, activating transcription factor 4 (ATF4), but not by the CHOP transcription factor. We identified the creatine kinase brain-type (

Indexed as

Unfolded Protein ResponseActivating Transcription Factor 4Adenosine TriphosphateApoptosisCreatine Kinase, BB FormeIF-2 KinaseHEK293 CellsHeLa CellsHomeostasisHumansMicroRNAsActivating Transcription Factor 4Adenosine TriphosphateATF4 protein, humanCreatine Kinase, BB FormEIF2AK3 protein, humaneIF-2 KinaseMicroRNAsMIRN483 microRNA, humanactivating transcription factor-4 (ATF-4)ATPcreatine kinase B (CKB)endoplasmic reticulum (ER)endoplasmic reticulum stress (ER stress)F1F0-ATPasefluorescence resonance energy transfer (FRET)microRNA (miRNA)PKR-like endoplasmic reticulum kinase (PERK)stress responsetranslationtranslation controlunfolded protein response (UPR)

Identifiers

PMID31792031
PMCPMC6952592
OpenAlexW2992985715

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.