Evidence map›Paper›PMID 26052671›Full record

ArticleeLife2015

The unfolded protein response is required for dendrite morphogenesis.

Xing Wei, Audrey S Howell, Xintong Dong, Caitlin A Taylor, Roshni C Cooper, Jianqi Zhang, Wei Zou, David R Sherwood, Kang Shen

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. 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
2.0field-weighted citation impact, top 15% 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, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Neuronal regulatedeLife · 2021
    Article
  13. STAR protocols · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. AG3 (Bethesda, Md.) · 2020
    Article
  18. Homeostatic Roles of the Proteostasis Network in Dendrites.Frontiers in cellular neuroscience · 2020
    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

9 authors at 4 institutions in 1 country.

Xing WeiDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Audrey S HowellDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Xintong DongDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Caitlin A TaylorDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Roshni C CooperDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Jianqi ZhangDivision of Biostatistics, Department of Preventive Medicine, University of Southern California, Los Angeles, United States.
Wei ZouDepartment of Biology, Duke University, Durham, United States.
David R SherwoodDepartment of Biology, Duke University, Durham, United States.
Kang ShenDepartment of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.
Howard Hughes Medical Institute · USDuke University · USStanford University · USUniversity of Southern California · US

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
Training Program in Developmental & Stem Cell BiologyT32HD040372 · NICHD · DUKE UNIVERSITY · PI Terry H Lechler · 2001 to 2026
$8.9M
Patterning dendritic branches with environmental and neuronal surface moleculesR01NS082208 · NINDS · STANFORD UNIVERSITY · PI KANG SHEN · 2013 to 2026
$4.1M
Understanding How Invadosomes Breach Basement Membrane In VivoR01GM100083 · NIGMS · DUKE UNIVERSITY · PI SHERWOOD, DAVID R · 2012 to 2015
$1.1M
Howard Hughes Medical InstituteNICHD NIH HHS T32 HD040372NIGMS NIH HHS R01 GM100083NIMH NIH HHS T32 MH020016NINDS NIH HHS 1R01NS082208NINDS NIH HHS 5R01NS082208-02NINDS NIH HHS R01 NS082208
6 · The paper itself

Abstract

Precise patterning of dendritic fields is essential for the formation and function of neuronal circuits. During development, dendrites acquire their morphology by exuberant branching. How neurons cope with the increased load of protein production required for this rapid growth is poorly understood. Here we show that the physiological unfolded protein response (UPR) is induced in the highly branched Caenorhabditis elegans sensory neuron PVD during dendrite morphogenesis. Perturbation of the IRE1 arm of the UPR pathway causes loss of dendritic branches, a phenotype that can be rescued by overexpression of the ER chaperone HSP-4 (a homolog of mammalian BiP/grp78). Surprisingly, a single transmembrane leucine-rich repeat protein, DMA-1, plays a major role in the induction of the UPR and the dendritic phenotype in the UPR mutants. These findings reveal a significant role for the physiological UPR in the maintenance of ER homeostasis during morphogenesis of large dendritic arbors.

Indexed as

MorphogenesisProtein BiosynthesisUnfolded Protein ResponseAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDendritesEndoribonucleasesMembrane ProteinsCaenorhabditis elegans ProteinsDMA-1 protein, C elegansEndoribonucleasesMembrane ProteinsC. eleganscell biologydendrite morphogenesisleucine rich repeatneuroscienceunfolded protein response

Identifiers

PMID26052671
PMCPMC4484204
OpenAlexW1947792139

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.