Evidence map›Paper›PMID 28441531›Full record

ArticleDevelopmental cell2017

Myrf ER-Bound Transcription Factors Drive C. elegans Synaptic Plasticity via Cleavage-Dependent Nuclear Translocation.

Jun Meng, Xiaoxia Ma, Huaping Tao, Xia Jin, Daniel Witvliet, James Mitchell, Ming Zhu, Meng-Qiu Dong, Mei Zhen, Yishi Jin and 1 more

Open access · greenAbstract read
In one paragraph

Article in Developmental cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. A molecular timer couples organism-wide temporal identity to developmental checkpoints.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Exploration (Beijing, China) · 2026
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  4. A developmental timer coordinates organism-wide microRNA transcription.bioRxiv : the preprint server for biology · 2026
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  6. Non-apoptotic death of thebioRxiv : the preprint server for biology · 2025
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  7. The NHR-23-regulated putative protease inhibitorbioRxiv : the preprint server for biology · 2024
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  8. Review
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  12. The epithelial NaCell reports · 2023
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  18. Interactive Repression of MYRF Self-Cleavage and Activity in Oligodendrocyte Differentiation by TMEM98 Protein.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 3 countries.

Jun MengInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China; Department of Physiology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Xiaoxia MaInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China.
Huaping TaoInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China.
Xia JinInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China.
Daniel WitvlietDepartment of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
James MitchellDepartment of Physics, Harvard University, Cambridge, MA 02138, USA.
Ming ZhuNational Institute of Biological Sciences, Beijing, Beijing 102206, China.
Meng-Qiu DongNational Institute of Biological Sciences, Beijing, Beijing 102206, China.
Mei ZhenDepartment of Physiology, University of Toronto, Toronto, ON M5S 1A8, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada.
Yishi JinHoward Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093, USA; Neurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Yingchuan B QiInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China. Electronic address: ybq@hznu.edu.cn.
Hangzhou Normal University · CNNational Institute of Biological Sciences, Beijing · CNHarvard University · USHoward Hughes Medical Institute · USMount Sinai Hospital · CAUniversity of Toronto · CA

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
GABAERGIC NEURON DIFFERENTIATION IN C ELEGANSR01NS035546 · NINDS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JIN, YISHI · 1996 to 2016
$5.3M
CIHR MOP-93619Howard Hughes Medical InstituteNIH HHS P40 OD010440NINDS NIH HHS R01 NS035546
6 · The paper itself

Abstract

Synaptic refinement is a critical step in nervous system maturation, requiring a carefully timed reorganization and refinement of neuronal connections. We have identified myrf-1 and myrf-2, two C. elegans homologs of Myrf family transcription factors, as key regulators of synaptic rewiring. MYRF-1 and its paralog MYRF-2 are functionally redundant specifically in synaptic rewiring. They co-exist in the same protein complex and act cooperatively to regulate synaptic rewiring. We find that the MYRF proteins localize to the ER membrane and that they are cleaved into active N-terminal fragments, which then translocate into the nucleus to drive synaptic rewiring. Overexpression of active forms of MYRF is sufficient to accelerate synaptic rewiring. MYRF-1 and MYRF-2 are the first genes identified to be indispensable for promoting synaptic rewiring in C. elegans. These findings reveal a molecular mechanism underlying synaptic rewiring and developmental circuit plasticity.

Indexed as

Active Transport, Cell NucleusAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell NucleusEndoplasmic ReticulumMembrane ProteinsNeuronal PlasticitySynapsesTranscription FactorsCaenorhabditis elegans ProteinsMembrane ProteinsTranscription Factorscritical periodER localizationER to nuclear translocationGABAergic motor neuronintramolecular chaperone of endosialidaselarval developmentproteolytic cleavagesynapse refinementsynaptic rewiring

Identifiers

PMID28441531
PMCPMC5493483
OpenAlexW2607735498

What OpenQuestion holds

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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.