Evidence map›Paper›PMID 39824639›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Large Donor CRISPR for Whole-Coding Sequence Replacement of Cell Adhesion Molecule LRRTM2.

Stephanie L Pollitt, Aaron D Levy, Michael C Anderson, Thomas A Blanpied

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. 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

4 authors.

Stephanie L PollittDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1509.ORCID 0000-0002-9297-6275
Aaron D LevyDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1509.ORCID 0000-0002-5856-8294
Michael C AndersonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1509.ORCID 0000-0001-8746-4681
Thomas A BlanpiedDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1509 tblanpied@som.umaryland.edu.ORCID 0000-0003-4957-557X

Funding

Internal Dynamics of the Postsynaptic DensityR37MH080046 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI Thomas A Blanpied · 2020 to 2026
$5.0M
Dynamic control of synapse organization and function by cleft-resident moleculesR01MH119826 · NIMH · YALE UNIVERSITY · PI BIEDERER, THOMAS, BLANPIED, THOMAS A · 2019 to 2023
$2.8M
Mechanisms of cell adhesion molecule LRRTM2 in basal and potentiated synaptic signalingF32MH130106 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI POLLITT, STEPHANIE LYNN · 2022 to 2024
$218k
Subsynaptic organization of the major NMDAR subtypesF31MH124283 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI ANDERSON, MICHAEL C. · 2021 to 2023
$128k
NIMH NIH HHS F31 MH124283NIMH NIH HHS F32 MH130106NIMH NIH HHS R01 MH119826NIMH NIH HHS R37 MH080046
6 · The paper itself

Abstract

The cell adhesion molecule leucine-rich repeat transmembrane neuronal protein 2 (LRRTM2) is crucial for synapse development and function. However, our understanding of its endogenous trafficking has been limited due to difficulties in manipulating its coding sequence (CDS) using standard genome editing techniques. Instead, we replaced the entire LRRTM2 CDS by adapting a two-guide CRISPR knock-in method, enabling complete control of LRRTM2. In primary rat hippocampal cultures dissociated from embryos of both sexes, N-terminally tagged, endogenous LRRTM2 was found in 80% of synapses, and synaptic LRRTM2 content correlated with PSD-95 and AMPAR levels. LRRTM2 was also enriched with AMPARs outside synapses, demonstrating the sensitivity of this method to detect relevant new biology. Finally, we leveraged total genomic control to increase the synaptic levels of LRRTM2 via simultaneous mutation of its C-terminal domain, which did not correspondingly increase AMPAR enrichment. The coding region of thousands of genes span lengths suitable for whole-CDS replacement, suggesting this simple approach will enable straightforward structure-function analysis in neurons.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsGene EditingMembrane ProteinsNerve Tissue ProteinsAnimalsCells, CulturedDisks Large Homolog 4 ProteinFemaleGene Knock-In TechniquesHippocampusMaleNeuronsRatsRats, Sprague-DawleyReceptors, AMPADisks Large Homolog 4 ProteinMembrane ProteinsNerve Tissue ProteinsReceptors, AMPAALFA tagAMPA receptorscell adhesion moleculesconditional reporterCRISPRknock-inLRRTM2neuronprotein structure–function analysisprotein traffickingsynapse biology

Identifiers

PMID39824639
PMCPMC11823385

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.