Evidence map›Paper›PMID 41058046›Full record

ArticleBrain : a journal of neurology2026

EIPR1 variants cause a neurodevelopmental disorder with endolysosomal and dense core vesicle defects.

Saikat Ghosh, Jaskaran Singh, Nadirah S Damseh, Mariasavina Severino, Raffaella De Pace, Adriana E Golding, Michal Jarnik, Poonam Thakran, Laurence Faivre, Jade Heitz and 24 more

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

34 authors.

Saikat GhoshDivision of Neuroscience and Cellular Structure, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Jaskaran SinghINRS-Centre Armand Frappier Santé Biotechnologie, Laval, QC H7V 1B7, Canada.
Nadirah S DamsehDepartment of Pediatrics & Genetics, Makassed Hospital, Al-Quds Medical School, East Jerusalem 95908, Palestine.
Mariasavina SeverinoNeuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genoa 16147, Italy.ORCID 0000-0003-4730-5322
Raffaella De PaceDivision of Neuroscience and Cellular Structure, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Adriana E GoldingDivision of Neuroscience and Cellular Structure, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Michal JarnikDivision of Neuroscience and Cellular Structure, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Poonam ThakranNational Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Laurence FaivreUniversité Bourgogne Europe, CHU Dijon Bourgogne, Centre de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU-TRANSLAD, Centre de Recherche Translationnelle en Médecine Moléculaire-Inserm UMR1231 équipe GAD, Dijon 21070, France.
Jade HeitzUniversité Bourgogne Europe, CHU Dijon Bourgogne, Centre de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU-TRANSLAD, Centre de Recherche Translationnelle en Médecine Moléculaire-Inserm UMR1231 équipe GAD, Dijon 21070, France.
Anne-Sophie Denommé-PichonUniversité Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, FHU-TRANSLAD, Centre de Recherche Translationnelle en Médecine Moléculaire-Inserm UMR1231 équipe GAD, Dijon 21070, France.ORCID 0000-0002-8986-8222
Antonio VitobelloUniversité Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, FHU-TRANSLAD, Centre de Recherche Translationnelle en Médecine Moléculaire-Inserm UMR1231 équipe GAD, Dijon 21070, France.ORCID 0000-0003-3717-8374
Lama AlAbdiDepartment of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh 12713, Saudi Arabia.
Firdous AbdulwahabDepartment of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh 12713, Saudi Arabia.
Safia SumayliDepartment of Medicine, Allergy and Immunology Section, King Faisal Specialist Hospital and Research Centre, Riyadh 12713, Saudi Arabia.
Mashael AlqahtaniDepartment of Translational Genomics, Genomic Medicine Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh 12713, Saudi Arabia.
Huma Arshad CheemaDepartment of Paediatric Gastroenterology, Hepatology and Genetic Diseases, Children's Hospital, University of Child Health Sciences, Lahore, Punjab 54000, Pakistan.
Iram JavedDepartment of Paediatric Neurology, Children Hospital and Institute of Child Health, Faisalabad 38000, Pakistan.
JiHye KimDivision of Medical Genetics, 3billion, Inc., Seoul 06160, South Korea.
Hanns LochmüllerDivision of Neurology, Department of Medicine, Children's Hospital of Eastern Ontario Research Institute, The Ottawa Hospital, Brain and Mind Research Institute, University of Ottawa, Ottawa, Ontario, Canada K1H 8L1.
Hagar Mor-ShakedDepartment of Genetics, Hadassah Medical Center, Jerusalem 91120, Israel.
Jennifer E NeilDivision of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
Ganeshwaran H MochidaDivision of Genetics and Genomics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
Giovanni ZifarelliCENTOGENE GmbH, Rostock 18055, Germany.
Peter BauerCENTOGENE GmbH, Rostock 18055, Germany.
Ehsan BarkhordariDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Ehsan Ghayoor KarimianiDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Henry HouldenDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.ORCID 0000-0002-2866-7777
Bassam Abu-LibdehDepartment of Pediatrics & Genetics, Makassed Hospital, Al-Quds Medical School, East Jerusalem 95908, Palestine.
Simon EdvardsonDepartment of Pediatrics, Neuropediatric Unit, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Orly ElpelegDepartment of Genetics, Hadassah Medical Center, Jerusalem 91120, Israel.
Reza MaroofianDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.ORCID 0000-0001-6763-1542
Shunmoogum A PattenINRS-Centre Armand Frappier Santé Biotechnologie, Laval, QC H7V 1B7, Canada.
Juan S BonifacinoDivision of Neuroscience and Cellular Structure, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Funding

Protein Trafficking In The Endosomal-Lysosomal SystemZIAHD001607 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BONIFACINO, JUAN · 2009 to 2025
$48.3M
a Brain Canada scholarshipEunice Kennedy Shriver National Institute of Child Health and Human Development OGB-177940European Reference Network(s) ITHACAEuropean Union Seventh Framework Programme 305444European Union Seventh Framework Programme FP7/2007-2013Horizon 2020 779257Intramural NIH HHS ZIA HD001607
6 · The paper itself

Abstract

EIPR1 (EARP-interacting protein 1, formerly known as tumor suppressing subtransferable candidate 1 or TSSC1) is a WD40-domain protein that interacts with the EARP (endosome-associated recycling protein) and GARP (Golgi-associated retrograde protein) complexes in the process of delivering endosome-derived transmembrane cargos to the plasma membrane and the trans-Golgi network (TGN), respectively. Additionally, EIPR1 cooperates with EARP in the biogenesis of dense core vesicles. While these properties of EIPR1 were established in cultured cells and model organisms, the physiological and pathological importance of EIPR1 in humans remains to be determined. Here, we report the identification of five EIPR1 homozygous missense variants [NM_003310.5:c.835C>G p.(Arg279Gly), NM_003310.5:c.813C>G p.(His271Gln), NM_003310.5:c.694C>T p.(Arg232Trp), NM_003310.5:c.47G>A p.(Arg16His) and NM_003310.5:c.419T>A p.(Val140Asp)] in eight individuals from six unrelated families with a neurological disorder featuring a spectrum of global neurodevelopmental delay, microcephaly, ataxia, spasticity, delayed myelination, callosal hypoplasia, cerebellar atrophy, walking and speech impairments, dysmorphic facies and neutropenia. Cellular studies using a heterologous transfection system demonstrate that these variants reduce EIPR1 protein levels and its physical interaction with EARP and GARP complexes. Furthermore, we show that the Arg279Gly and His271Gln variants reduce the ability of EIPR1 to promote EARP association with endosomes in non-neuronal cells and dense core vesicle biogenesis in induced pluripotent stem cell-derived neurons. Additionally, skin fibroblasts from one of the Arg279Gly affected individuals shows reduced recycling of internalized transferrin to the plasma membrane (an EARP-deficiency phenotype) and impaired retrograde transport of internalized Shiga toxin B-subunit to the TGN (a GARP-deficiency phenotype) compared with fibroblasts from an unaffected parent. Moreover, these patient fibroblasts exhibit enlarged lysosomes, increased levels of the lysosomal membrane protein LAMP1, and increased levels of the autophagic markers LC3B-II and SQSTM1, all phenotypes previously associated with GARP deficiency. Knockout (KO) of the orthologous eipr1 in zebrafish results in neurodevelopmental and locomotor defects consistent with the clinical phenotype of the human patients. Injection of wild-type human EIPR1 mRNA into eipr1 KO zebrafish rescues these defects, whereas mRNAs encoding the human EIPR1 variants Arg279Gly or His271Gln fail to do so, confirming the impaired activity of these variants. These findings identify EIPR1 as a novel genetic locus associated with a neurodevelopmental disorder and underscore its critical role in endosomal recycling and dense core vesicle biogenesis, processes essential for the development and function of the nervous system.

Indexed as

EndosomesLysosomesNeurodevelopmental DisordersAdolescentAdultChildChild, PreschoolFemaleHumansMaleMutation, MissenseVesicular Transport ProteinsVesicular Transport Proteinsdense core vesicleEARPendosomesGARPGolgiTSSC1

Identifiers

PMID41058046
PMCPMC13140528

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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.