Evidence map›Paper›PMID 41993462›Full record

ArticlebioRxiv : the preprint server for biology2026

Human-specific multicopy gene FRMPD2 promotes synapse formation via recruitment of neuroligin 1.

Yuda Huo, Ameya Patkar, KathrynAnn Merth, James Gilbert, Heng-Ye Man

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Yuda HuoDepartment of Biology, Boston University, Boston, MA 02215 USA.ORCID 0000-0002-5318-6756
Ameya PatkarDepartment of Biology, Boston University, Boston, MA 02215 USA.ORCID 0000-0002-2648-3659
KathrynAnn MerthDepartment of Biology, Boston University, Boston, MA 02215 USA.ORCID 0000-0002-7583-470X
James GilbertDepartment of Biology, Boston University, Boston, MA 02215 USA.ORCID 0000-0002-0947-4654
Heng-Ye ManDepartment of Biology, Boston University, Boston, MA 02215 USA.ORCID 0000-0002-3530-3066

Funding

Molecular Mechanisms of Homeostatic Synaptic PlasticityR01MH079407 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MAN, HENGYE · 2008 to 2018
$3.9M
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 MH079407NIMH NIH HHS R01 MH130600NIMH NIH HHS R21 MH133014NIMH NIH HHS R21 MH134174
6 · The paper itself

Abstract

FRMPD2 is a human-specific multi-copy gene with higher mRNA expression in brain tissue, but its role in synapse formation and neurodevelopment remains unknown. We find that FRMPD2 is a neuron-specific protein with a high expression level in human brains compared to rodent brains. FRMPD2 overexpression in rat neurons stimulates synaptogenesis, leading to increased synaptic activities. Importantly, our results show that FRMPD2 via its PDZ domains recruits and enhances neuroligin-1 protein levels at the postsynaptic sites, and via its FERM domain interacts with the F-actin network in the spine. Increased expression of FRMPD2 also promotes spine formation and maturation, a foundational process for synapse formation. In developing embryonic mouse brains expressing higher FRMPD2 protein levels, we observed delayed neuronal migration, presumably promoting a protracted timeline for cortical lamination as a feature in human brain development. Behaviorally, mice with FRMPD2 overexpression in the brain demonstrate enhanced spatial memory retention. These findings indicate an important function for FRMPD2 in neuronal connectivity, brain development, and cognitive function.

Identifiers

PMID41993462
PMCPMC13081824

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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.