Evidence map›Paper›PMID 42320471›Full record

ArticleAmerican journal of human genetics2026

De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanisms.

Rebecca Fluri, Mireia Coll-Tané, Theresa Brunet, Benjamin Cogne, Solene Conrad, Mathilde Nizon, Francesco Nicita, Lorena Travaglini, Antonio Novelli, Margie Glissmeyer and 31 more

Abstract read
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Article in American journal of human genetics, 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

41 authors.

Rebecca FluriDepartment of Human Genetics, Inselspital University Hospital Bern, University of Bern, 3010 Bern, Switzerland; Department for Biomedical Research (DBMR), University of Bern, 3010 Bern, Switzerland.
Mireia Coll-TanéDepartment of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.
Theresa BrunetTUM School of Medicine and Health, Institute of Human Genetics, TUM University Hospital, Technical University of Munich, 81675 Munich, Germany.
Benjamin CogneNantes Université, CHU de Nantes, Service de Génétique Médicale, 44000 Nantes, France; Nantes Université, CHU de Nantes, CNRS, INSERM, L'institut du Thorax, 44000 Nantes, France.
Solene ConradNantes Université, CHU de Nantes, Service de Génétique Médicale, 44000 Nantes, France.
Mathilde NizonNantes Université, CHU de Nantes, Service de Génétique Médicale, 44000 Nantes, France.
Francesco NicitaUnit of Muscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Lorena TravagliniLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Antonio NovelliLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Margie GlissmeyerSeattle Children's Hospital, Seattle, WA 98105, USA.
Amanda PetersonSeattle Children's Hospital, Seattle, WA 98105, USA; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR 97239, USA.
Jillian G BuchanDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA.
Dan SerberDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA.
Kolja MeierDepartment of Pediatrics and Adolescent Medicine, Division Pediatric Neurology and German Center for Child and Adolescent Health (DZKJ), University Medical Center Göttingen, 37075 Göttingen, Germany.
Jutta GärtnerDepartment of Pediatrics and Adolescent Medicine, Division Pediatric Neurology and German Center for Child and Adolescent Health (DZKJ), University Medical Center Göttingen, 37075 Göttingen, Germany.
Susann DiegmannDepartment of Pediatrics and Adolescent Medicine, Division Pediatric Neurology and German Center for Child and Adolescent Health (DZKJ), University Medical Center Göttingen, 37075 Göttingen, Germany.
Veronique PingaultService de Médecine Génomique des Maladies Rares, AP-HP Centre, Hôpital Necker-Enfants Malades, 75015 Paris, France.
Tania Attie-BitachService de Médecine Génomique des Maladies Rares, AP-HP Centre, Hôpital Necker-Enfants Malades, 75015 Paris, France.
Thomas CourtinCenter for Molecular and Chromosomal Genetics, AP-HP-Sorbonne University, Pitié-Salpêtrière Hospital, 75013 Paris, France.
Michael C SchneiderSection of Neurology, Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA 19134, USA.
Wing HungSection of Neurology, Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA 19134, USA.
Inderneel SahaiDivision of Medical Genetics and Metabolism, Massachusetts General Hospital for Children, Boston, MA 02114, USA.
Lauren O'GradyDivision of Medical Genetics and Metabolism, Massachusetts General Hospital for Children, Boston, MA 02114, USA.
Katharina SteindlInstitute of Medical Genetics, University of Zurich, 8952 Zurich, Switzerland.
Sarju G MehtaDepartment of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, and University of Cambridge, Cambridge CB2 0QQ, UK.
Christel DepienneInstitute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, 45122 Essen, Germany.
Delphine HeronDépartement de Génétique, AP-HP-Sorbonne Université, Hôpital Trousseau & Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France.
Boris KerenDépartement de Génétique, AP-HP-Sorbonne Université, Hôpital Trousseau & Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France.
Solveig HeideDépartement de Génétique, AP-HP-Sorbonne Université, Hôpital Trousseau & Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France.
Shane McKeeNorthern Ireland Regional Genetics Service, Belfast City Hospital, Belfast BT9 7AB, UK.
Franco LacconeCenter for Pathobiochemistry and Genetics, Institute of Medical Genetics, Medical University of Vienna, 1090 Vienna, Austria.
Lisa M DyerGeneDx, LLC, Gaithersburg, MD 20877, USA.
Catherine MelverDivision of Medical Genetics, Akron Children's Hospital, Akron, OH 44302, USA.
Connie MotterDivision of Medical Genetics, Akron Children's Hospital, Akron, OH 44302, USA.
Wendy D JonesThe North East Thames Regional Genetics Service, Great Ormond Street Hospital, London WC1N 3JH, UK.
Zoey Trueblood WilsonSouthern California Kaiser Permanente Regional Metabolic Genetics Center, Los Angeles, CA 90041, USA.
Divya VatsSouthern California Kaiser Permanente Regional Metabolic Genetics Center, Los Angeles, CA 90041, USA.
Kristina HußLMU Klinikum, Campus Innenstadt, Dr. von Haunersches Kinderspital und iSPZ Hauner MUC, 80337 München, Germany.
Christiane ZweierDepartment of Human Genetics, Inselspital University Hospital Bern, University of Bern, 3010 Bern, Switzerland; Department for Biomedical Research (DBMR), University of Bern, 3010 Bern, Switzerland.
Heinrich StichtInstitut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Anne GregorDepartment of Human Genetics, Inselspital University Hospital Bern, University of Bern, 3010 Bern, Switzerland; Department for Biomedical Research (DBMR), University of Bern, 3010 Bern, Switzerland. Electronic address: anne.gregor@unibe.ch.

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
DROSOPHILA GENOMICS RESOURCE CENTERP40OD010949 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Andrew Zelhof · 2012 to 2026
$9.4M
NIH HHS P40 OD010949NIH HHS P40 OD018537
6 · The paper itself

Abstract

LDB1 encodes transcriptional regulator protein LIM domain-binding protein 1, which plays an important role in neurogenesis. Few C-terminal likely gene-disrupting (LGD) variants have been reported in the literature in individuals with congenital ventriculomegaly. Through international collaboration, we now assembled a cohort of 16 individuals with de novo variants affecting various regions of LDB1. Eleven variants affect either the whole gene or the N-terminal dimerization domain (including gene deletions, as well as nonsense-mediated mRNA decay (NMD)-sensitive LGD and missense variants), and five variants (missense or NMD-escaping LGD variants) affect only the C terminus of LDB1 containing the LIM interaction domain. All individuals showed variable neurodevelopmental phenotypes, including developmental delay and behavioral anomalies. In line with literature reports, individuals harboring C-terminal variants additionally presented with ventriculomegaly, which suggests a potential genotype-phenotype correlation. In accordance, we found diverging pathomechanisms in vitro: N-terminal missense variants disrupt homodimerization of LDB1, likely leading to a loss of function, while C-terminal variants impair interaction with the essential partner LHX2 in a dominant-negative manner. These findings were confirmed in vivo in Drosophila melanogaster. Toxicity of overexpressed human LDB1 in Drosophila was not observed with N-terminal missense variants but was exacerbated by C-terminal variants. Similarly, phenotypes associated with LDB1/chi loss were rescued by overexpression of wild-type LDB1 but not by LDB1 harboring N-terminal missense variants or by C-terminal variants that even worsened phenotypes. In summary, our findings indicate that de novo variants in LDB1 are linked to two overlapping but distinct neurodevelopmental phenotypes based on variant location and propose two separate pathomechanisms underlying LDB1-related neurodevelopmental disorders.

Indexed as

DNA-Binding ProteinsNeurodevelopmental DisordersTranscription FactorsAnimalsChildChild, PreschoolDrosophila melanogasterFemaleGenetic Association StudiesHumansMaleMutation, MissenseNeurodevelopmentPhenotypeDNA-Binding ProteinsTranscription Factorsdisease gene discoveryDrosophila melanogasterneurodevelopmental disorderrare disease

Identifiers

PMID42320471
PMCPMC13504347

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