Evidence map›Paper›PMID 40892511›Full record

ArticleThe Journal of clinical investigation2025

A pathogenic variant of AMOT leads to isolated X-linked congenital hydrocephalus due to N-terminal truncation.

Nurcan Hastar, Hagit Daum, Nikoletta Kardos-Török, Gael Ganz, Leon Obendorf, Peter Vajkoczy, Orly Elpeleg, Petra Knaus

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. 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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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

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Nurcan HastarInstitute for Chemistry and Biochemistry, Freie Universitaet Berlin, Berlin, Germany.
Hagit DaumDepartment of Genetics, Hadassah Hebrew Medical Center and the Faculty of Medicine, Jerusalem, Israel.
Nikoletta Kardos-TörökInstitute for Chemistry and Biochemistry, Freie Universitaet Berlin, Berlin, Germany.
Gael GanzDepartment of Genetics, Hadassah Hebrew Medical Center and the Faculty of Medicine, Jerusalem, Israel.
Leon ObendorfInstitute for Chemistry and Biochemistry, Freie Universitaet Berlin, Berlin, Germany.
Peter VajkoczyDepartment of Neurosurgery with Pediatric Neurosurgery, Charité Universitätsmedizin, Berlin, Germany.
Orly ElpelegDepartment of Genetics, Hadassah Hebrew Medical Center and the Faculty of Medicine, Jerusalem, Israel.
Petra KnausInstitute for Chemistry and Biochemistry, Freie Universitaet Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital hydrocephalus is a life-threatening condition that might affect brain development by increasing the pressure on the brain parenchyma. Here, we describe 6 male patients from 1 family, all presenting with an isolated X-linked congenital hydrocephalus. Exome sequencing identified a likely pathogenic variant of angiomotin (AMOT) that segregated with the phenotype in the extended family. We show that the variant, affecting the first methionine, translated into a shorter AMOT protein lacking 91 amino acids from the N-terminus. Mechanistically, we unraveled that the absence of the N-terminus leads to abnormally increased AMOT protein levels due to the loss of both the N-degron degradation signal and the tankyrase-binding domain. Altered degradation of AMOT disrupted the barrier integrity of the cells. Thus, the identified AMOT variant likely underlies the clinical presentation of isolated X-linked hydrocephalus in this family, and our data underscore the importance of tight regulation of AMOT protein level in the brain. AMOT now joins the list of genes involved in congenital hydrocephalus in humans. These findings are instrumental for the genetic counseling of affected families.

Indexed as

AngiomotinsGenetic Diseases, X-LinkedHydrocephalusAdultCerebral AqueductDegronsExome SequencingFemaleFibroblastsGenetic CounselingHumansInfant, NewbornMagnetic Resonance ImagingMalePedigreePrimary Cell CultureAMOT protein, humanAngiomotinsCell biologyGenetic diseasesGeneticsMolecular diagnosisTight junctions

Identifiers

PMID40892511
PMCPMC12404752

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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.