Evidence map›Paper›PMID 28114319›Full record

ArticlePLoS genetics2017

Reduced Insulin/Insulin-Like Growth Factor Receptor Signaling Mitigates Defective Dendrite Morphogenesis in Mutants of the ER Stress Sensor IRE-1.

Yehuda Salzberg, Andrew J Coleman, Kevin Celestrin, Moran Cohen-Berkman, Thomas Biederer, Sivan Henis-Korenblit, Hannes E Bülow

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Neuronal regulatedeLife · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Type I interferons and endoplasmic reticulum stress in health and disease.International review of cell and molecular biology · 2020
    Review
  12. Review
  13. Article
  14. Review
  15. 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

7 authors at 3 institutions in 2 countries.

Yehuda SalzbergDepartment of Genetics, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Andrew J ColemanDepartment of Neuroscience, Tufts University School of Medicine, Boston, MA, United States of America.ORCID 0000-0003-4032-5283
Kevin CelestrinDepartment of Genetics, Albert Einstein College of Medicine, Bronx, New York, United States of America.ORCID 0000-0002-9872-0393
Moran Cohen-BerkmanThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Thomas BiedererDepartment of Neuroscience, Tufts University School of Medicine, Boston, MA, United States of America.
Sivan Henis-KorenblitThe Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.ORCID 0000-0001-8023-6336
Hannes E BülowDepartment of Genetics, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Albert Einstein College of Medicine · USBar-Ilan University · ILTufts University · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Support for the Rose F. Kennedy IDDRCU54HD090260 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WALKLEY, STEVEN UPSHAW · 2016 to 2020
$6.0M
Translational Neuroimaging CoreP30HD071593 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WALKLEY, STEVEN UPSHAW · 2011 to 2015
$5.6M
Molecular NeuropathologyT32NS007098 · NINDS · YESHIVA UNIVERSITY · PI SANTAMBROGIO, LAURA · 1985 to 2015
$5.0M
Mechanisms of SynCAM-Induced Synapse FormationR01DA018928 · NIDA · YALE UNIVERSITY · PI BIEDERER, THOMAS · 2005 to 2021
$4.6M
Genetic Analyses of Dendrite Development in Caenorhabditis elegansR01NS096672 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BUELOW, HANNES ERICH · 2016 to 2020
$1.8M
Synapse Neurobiology Training ProgramT32NS061764 · NINDS · TUFTS UNIVERSITY BOSTON · PI BIEDERER, THOMAS · 2009 to 2019
$1.7M
Establishing the Role of a Novel Conserved Gene in Dendrite MorphogenesisR21NS081505 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUELOW, HANNES ERICH · 2013 to 2014
$457k
NCI NIH HHS P30 CA013330NICHD NIH HHS P30 HD071593NICHD NIH HHS U54 HD090260NIDA NIH HHS R01 DA018928NIH HHS P40 OD010440NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS096672NINDS NIH HHS R21 NS081505NINDS NIH HHS T32 NS007098NINDS NIH HHS T32 NS061764
6 · The paper itself

Abstract

Neurons receive excitatory or sensory inputs through their dendrites, which often branch extensively to form unique neuron-specific structures. How neurons regulate the formation of their particular arbor is only partially understood. In genetic screens using the multidendritic arbor of PVD somatosensory neurons in the nematode Caenorhabditis elegans, we identified a mutation in the ER stress sensor IRE-1/Ire1 (inositol requiring enzyme 1) as crucial for proper PVD dendrite arborization in vivo. We further found that regulation of dendrite growth in cultured rat hippocampal neurons depends on Ire1 function, showing an evolutionarily conserved role for IRE-1/Ire1 in dendrite patterning. PVD neurons of nematodes lacking ire-1 display reduced arbor complexity, whereas mutations in genes encoding other ER stress sensors displayed normal PVD dendrites, specifying IRE-1 as a selective ER stress sensor that is essential for PVD dendrite morphogenesis. Although structure function analyses indicated that IRE-1's nuclease activity is necessary for its role in dendrite morphogenesis, mutations in xbp-1, the best-known target of non-canonical splicing by IRE-1/Ire1, do not exhibit PVD phenotypes. We further determined that secretion and distal localization to dendrites of the DMA-1/leucine rich transmembrane receptor (DMA-1/LRR-TM) is defective in ire-1 but not xbp-1 mutants, suggesting a block in the secretory pathway. Interestingly, reducing Insulin/IGF1 signaling can bypass the secretory block and restore normal targeting of DMA-1, and consequently normal PVD arborization even in the complete absence of functional IRE-1. This bypass of ire-1 requires the DAF-16/FOXO transcription factor. In sum, our work identifies a conserved role for ire-1 in neuronal branching, which is independent of xbp-1, and suggests that arborization defects associated with neuronal pathologies may be overcome by reducing Insulin/IGF signaling and improving ER homeostasis and function.

Indexed as

NeurogenesisSignal TransductionAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsCells, CulturedDendritesForkhead Transcription FactorsInsulinMembrane ProteinsProtein Serine-Threonine KinasesRatsReceptors, SomatomedinCaenorhabditis elegans ProteinsCarrier Proteinsdaf-16 protein, C elegansDMA-1 protein, C elegansForkhead Transcription FactorsInsulinIRE-1 protein, C elegansMembrane ProteinsProtein Serine-Threonine KinasesReceptors, SomatomedinXBP-1 protein, C elegans

Identifiers

PMID28114319
PMCPMC5293268
OpenAlexW2581993304

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.