Evidence map›Paper›PMID 29738713›Full record

ArticleDevelopmental cell2018

A Dendritic Guidance Receptor Complex Brings Together Distinct Actin Regulators to Drive Efficient F-Actin Assembly and Branching.

Wei Zou, Xintong Dong, Timothy R Broederdorf, Ao Shen, Daniel A Kramer, Rebecca Shi, Xing Liang, David M Miller, Yang K Xiang, Ryohei Yasuda and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 85 citations in OpenAlex.

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  4. The actin assembly regulatorbioRxiv : the preprint server for biology · 2025
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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

12 authors at 7 institutions in 2 countries.

Wei ZouThe Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu 322000, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310058, China; Howard Hughes Medical Institute, Department of Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: zouwei@zju.edu.cn.
Xintong DongHoward Hughes Medical Institute, Department of Biology, Stanford University, Stanford, CA 94305, USA.
Timothy R BroederdorfRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
Ao ShenDepartment of Pharmacology, University of California, Davis, CA 95616, USA.
Daniel A KramerRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
Rebecca ShiNeurosciences Program, Stanford University, Stanford, CA 94305, USA.
Xing LiangHoward Hughes Medical Institute, Department of Biology, Stanford University, Stanford, CA 94305, USA.
David M MillerDepartment of Cell and Developmental Biology and Program in Neuroscience, Vanderbilt University, Nashville, TN 37232, USA.
Yang K XiangDepartment of Pharmacology, University of California, Davis, CA 95616, USA; VA Northern California Health Care System, Mather, CA 95655, USA.
Ryohei YasudaMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Baoyu ChenRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA. Electronic address: stone@iastate.edu.
Kang ShenHoward Hughes Medical Institute, Department of Biology, Stanford University, Stanford, CA 94305, USA; National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China. Electronic address: kangshen@stanford.edu.
Howard Hughes Medical Institute · USIowa State University · USMax Planck Florida Institute for Neuroscience · USStanford University · USUniversity of California, Davis · USVanderbilt University · USVA Northern California Health Care System · US

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
Patterning dendritic branches with environmental and neuronal surface moleculesR01NS082208 · NINDS · STANFORD UNIVERSITY · PI KANG SHEN · 2013 to 2026
$4.1M
Molecular regulation of dendrite morphogenesisR01NS079611 · NINDS · VANDERBILT UNIVERSITY · PI MILLER, DAVID M · 2013 to 2017
$1.7M
NICHD NIH HHS U54 HD083211NIH HHS P40 OD010440NIMH NIH HHS T32 MH020016NINDS NIH HHS R01 NS079611NINDS NIH HHS R01 NS082208
6 · The paper itself

Abstract

Proper morphogenesis of dendrites plays a fundamental role in the establishment of neural circuits. The molecular mechanism by which dendrites grow highly complex branches is not well understood. Here, using the Caenorhabditis elegans PVD neuron, we demonstrate that high-order dendritic branching requires actin polymerization driven by coordinated interactions between two membrane proteins, DMA-1 and HPO-30, with their cytoplasmic interactors, the RacGEF TIAM-1 and the actin nucleation promotion factor WAVE regulatory complex (WRC). The dendrite branching receptor DMA-1 directly binds to the PDZ domain of TIAM-1, while the claudin-like protein HPO-30 directly interacts with the WRC. On dendrites, DMA-1 and HPO-30 form a receptor-associated signaling complex to bring TIAM-1 and the WRC to close proximity, leading to elevated assembly of F-actin needed to drive high-order dendrite branching. The synergistic activation of F-actin assembly by scaffolding distinct actin regulators might represent a general mechanism in promoting complex dendrite arborization.

Indexed as

Actin CytoskeletonAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell MembraneDendritesMembrane ProteinsMorphogenesisNeurogenesisSensory Receptor CellsSignal TransductionCaenorhabditis elegans ProteinsDMA-1 protein, C elegansMembrane Proteinswve-1 protein, C elegansactindendrite branchingDMA-1HPO-30RacreceptorsynergyTIAM-1WAVE regulatory complex

Identifiers

PMID29738713
PMCPMC6292511
OpenAlexW2799820360

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.