Evidence map›Paper›PMID 35139179›Full record

ArticleBrain : a journal of neurology2022

Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology.

Siddharth Banka, Abigail Bennington, Martin J Baker, Ellen Rijckmans, Giuliana D Clemente, Nurhuda Mohamad Ansor, Hilary Sito, Pritha Prasad, Kwame Anyane-Yeboa, Lauren Badalato and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. A matter of switch: how RAC1 variants drive distinct disorders.European journal of human genetics : EJHG · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. ARP2/3 complex mediates the neuropathology of PTEN-deficient human neural cells downstream of mTORC1 and mTORC2 hyperactivation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. RAC1 signaling in prostate cancer: VAV GEFs take center stage.Frontiers in cell and developmental biology · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. An unusual presentation of de novo RAC3 variation in prenatal diagnosis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  18. Article
  19. Presynaptic Rac1 in the hippocampus selectively regulates working memory.bioRxiv : the preprint server for biology · 2024
    Article
  20. Genes · 2023
    Review
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

25 authors at 13 institutions in 6 countries.

Siddharth BankaDivision of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0002-8527-2210
Abigail BenningtonDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.
Martin J BakerDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Ellen RijckmansDepartment of Pediatrics, UZ Brussel, Brussels, Belgium.
Giuliana D ClementeDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.
Nurhuda Mohamad AnsorDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.
Hilary SitoDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.
Pritha PrasadDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.
Kwame Anyane-YeboaDivision of Clinical Genetics, Columbia University Medical Center, New York 10032, USA.
Lauren BadalatoDepartment of Pediatrics, School of Medicine, Kingston General Hospital, Queen's University, Kingston, ON, Canada.
Boyan DimitrovCentre for Medical Genetics, UZ Brussel, Brussels, Belgium.
David FitzpatrickMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
Anna C E HurstDepartment of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
Anna C JansenNeurogenetics Research Group, Vrije Universiteit Brussel, Brussels, Belgium.
Melissa A KellyHudsonAlpha Clinical Services Lab, Huntsville, AL, USA.
Ian KrantzRoberts Individualized Medical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Claudine RieublandDepartment of Human Genetics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Meredith RossDivision of Clinical Genetics, Columbia University Medical Center, New York 10032, USA.ORCID 0000-0001-8502-2839
Natasha L RudyDepartment of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
Javier SanzDepartment of Human Genetics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Katrien StouffsNeurogenetics Research Group, Vrije Universiteit Brussel, Brussels, Belgium.
Zhuo Luan XuRoberts Individualized Medical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Angeliki MalliriCell Signalling Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, Macclesfield SK10 4TG, UK.
Marcelo G KazanietzDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Tom H MillardDivision of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.ORCID 0000-0002-8869-4654
University of Manchester · GBVrije Universiteit Brussel · BEChildren's Hospital of Philadelphia · USColumbia University Irving Medical Center · USUniversity of Alabama at Birmingham · USUniversity of Bern · CHHudsonAlpha Institute for Biotechnology · USInstitute of Genetics and Cancer · GBManchester Academic Health Science Centre · GBQueen's University · CATranslational Therapeutics (United States) · USUniversitair Ziekenhuis Brussel · BEUniversiti Sains Malaysia · MY

Funding

Cancer Research UK 20410Wellcome Trust 201958/Z/16/ZWellcome Trust WT098051
6 · The paper itself

Abstract

RAC1 is a highly conserved Rho GTPase critical for many cellular and developmental processes. De novo missense RAC1 variants cause a highly variable neurodevelopmental disorder. Some of these variants have previously been shown to have a dominant negative effect. Most previously reported patients with this disorder have either severe microcephaly or severe macrocephaly. Here, we describe eight patients with pathogenic missense RAC1 variants affecting residues between Q61 and R68 within the switch II region of RAC1. These patients display variable combinations of developmental delay, intellectual disability, brain anomalies such as polymicrogyria and cardiovascular defects with normocephaly or relatively milder micro- or macrocephaly. Pulldown assays, NIH3T3 fibroblast spreading assays and staining for activated PAK1/2/3 and WAVE2 suggest that these variants increase RAC1 activity and over-activate downstream signalling targets. Axons of neurons isolated from Drosophila embryos expressing the most common of the activating variants are significantly shorter, with an increased density of filopodial protrusions. In vivo, these embryos exhibit frequent defects in axonal organization. Class IV dendritic arborization neurons expressing this variant exhibit a significant reduction in the total area of the dendritic arbour, increased branching and failure of self-avoidance. RNAi knock down of the WAVE regulatory complex component Cyfip significantly rescues these morphological defects. These results establish that activating substitutions affecting residues Q61-R68 within the switch II region of RAC1 cause a developmental syndrome. Our findings reveal that these variants cause altered downstream signalling, resulting in abnormal neuronal morphology and reveal the WAVE regulatory complex/Arp2/3 pathway as a possible therapeutic target for activating RAC1 variants. These insights also have the potential to inform the mechanism and therapy for other disorders caused by variants in genes encoding other Rho GTPases, their regulators and downstream effectors.

Indexed as

MegalencephalyNeurodevelopmental Disordersrac1 GTP-Binding ProteinAnimalsMiceNeuronsNIH 3T3 CellsSignal Transductionrac1 GTP-Binding Proteinintellectual disabilitypolymicrogyriaRAC1small GTPasesWAVE regulatory complex

Identifiers

PMID35139179
PMCPMC9762944
OpenAlexW4210916782

What OpenQuestion holds

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Registered trials

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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.