Evidence map›Paper›PMID 41053001›Full record

ArticleTranslational psychiatry2025

Restoration of NEXMIF expression rescues abnormalities in gene transcription, neuron maturation and autistic-like behaviors in Nexmif knockout mice.

KathrynAnn Odamah, Heng-Ye Man

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

2 authors.

KathrynAnn OdamahDepartment of Biology, Boston University, 5 Cummington Mall, Boston, MA, 02215, USA.ORCID http://orcid.org/0000-0002-7583-470X
Heng-Ye ManDepartment of Biology, Boston University, 5 Cummington Mall, Boston, MA, 02215, USA. hman@bu.edu.ORCID http://orcid.org/0000-0002-3530-3066

Funding

Molecular mechanisms of homeostatic synaptic plasticityR01MH130600 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Hengye Man · 2023 to 2026
$1.9M
Study of NEXMIF mosaic expression on neuronal development and connectivity in female miceR21MH133014 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MAN, HENGYE · 2023 to 2024
$454k
Exploring the Rescue Strategy for Female NEXMIF Haploinsufficiency via X Chromosome ReactivationR21MH134174 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MAN, HENGYE · 2024 to 2024
$445k
NIMH NIH HHS R01 MH130600NIMH NIH HHS R21 MH133014NIMH NIH HHS R21 MH134174
6 · The paper itself

Abstract

NEXMIF is an X-linked gene implicated in encephalopathy with symptoms of autism spectrum disorder (ASD), intellectual disability, and seizures. Our previous work demonstrated that Nexmif knockout (KO) male mice show autistic-like behaviors and memory deficits, accompanied by significant abnormalities in neuronal development and function. However, to date there are no available therapeutics for NEXMIF-related disorders. Here, as a proof-of-concept study, we examined the effect of postnatal reintroduction of the NEXMIF gene as a strategy for rescuing the impaired cellular and behavioral phenotypes in KO mice. We find that injection of a human NEXMIF lentivirus into KO mouse brains at postnatal day 1 (P1) leads to a restoration in synaptic protein expression and formation of dendritic spines. More importantly, postnatal NEXMIF expression ameliorated behavioral defects in repetitive behavior, sociability, social novelty preference, and cognition at adolescent ages, in addition to restoring dysregulated gene expression. These findings suggest that gene reintroduction at a postnatal stage may serve as a rescue strategy for neurodevelopmental and behavioral deficits caused by NEXMIF deficiencies.

Indexed as

Autism Spectrum DisorderAutistic DisorderBehavior, AnimalNeuronsTranscription, GeneticAnimalsBrainDendritic SpinesDisease Models, AnimalHumansMaleMiceMice, KnockoutNeurogenesisSocial Behavior

Identifiers

PMID41053001
PMCPMC12501234

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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.