Evidence map›Paper›PMID 41271436›Full record

ArticleeNeuro2025

Multiplexed smFISH Reveals the Spatial Organization of Neuropil Localized mRNAs Is Linked to Abundance.

Renesa Tarannum, Grace Mun, Fatima Quddos, Sharon A Swanger, Oswald Steward, Shannon Farris

Abstract read
In one paragraph

Article in eNeuro, 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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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

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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

5 · Who and what money

Authors and funding

6 authors.

Renesa TarannumFralin Biomedical Research Institute at Virginia Tech Carilion, Center for Neurobiology Research, Roanoke, Virginia 24016.ORCID https://orcid.org/0000-0002-6797-5799
Grace MunFralin Biomedical Research Institute at Virginia Tech Carilion, Center for Neurobiology Research, Roanoke, Virginia 24016.ORCID https://orcid.org/0009-0007-0282-3157
Fatima QuddosFralin Biomedical Research Institute at Virginia Tech Carilion, Center for Neurobiology Research, Roanoke, Virginia 24016.ORCID https://orcid.org/0000-0003-3866-5780
Sharon A SwangerFralin Biomedical Research Institute at Virginia Tech Carilion, Center for Neurobiology Research, Roanoke, Virginia 24016.ORCID https://orcid.org/0000-0003-0615-6244
Oswald StewardDepartment of Anatomy & Neurobiology, University of California Irvine School of Medicine, Irvine, California 92697.ORCID https://orcid.org/0000-0001-7069-8756
Shannon FarrisFralin Biomedical Research Institute at Virginia Tech Carilion, Center for Neurobiology Research, Roanoke, Virginia 24016 farrissl@vtc.vt.edu.ORCID https://orcid.org/0000-0003-4473-1684

Funding

POST-LESION PLASTICITY OF NEURONAL CIRCUITRYR01NS012333 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI STEWARD, OSWALD · 1985 to 2011
$3.2M
Cell-Type Specific Regulation of Dendritic mRNA in the HippocampusR00MH109626 · NIMH · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI FARRIS, SHANNON · 2019 to 2021
$795k
NIMH NIH HHS R00 MH109626NINDS NIH HHS R01 NS012333
6 · The paper itself

Abstract

RNA localization to neuronal axons and dendrites provides spatiotemporal control over gene expression to support synapse function. Neuronal messenger RNAs (mRNAs) localize as ribonucleoprotein particles (RNPs), commonly known as RNA granules, the composition of which influences when and where proteins are made. High-throughput sequencing has revealed thousands of mRNAs that localize to the hippocampal neuropil. Whether these mRNAs are spatially organized into common RNA granules or distributed as independent mRNAs for proper delivery to synapses is debated. Here, using highly multiplexed single-molecule fluorescence in situ hybridization (HiPlex smFISH) and colocalization analyses, we investigate the subcellular spatial distribution of 15 synaptic neuropil localized mRNAs in the male and female rodent hippocampus. We observed that these mRNAs are present in the neuropil as heterogeneously sized fluorescent puncta with spatial colocalization patterns that generally scale by neuropil mRNA abundance. Indeed, differentially expressed mRNAs across cell types displayed colocalization patterns that scaled by abundance, as did simulations that reproduce cell-specific differences in abundance. Thus, the probability of these mRNAs colocalizing in the neuropil is best explained by stochastic interactions based on abundance, which places constraints on the mechanisms mediating efficient transport to synapses.

Indexed as

HippocampusNeuropilRNA, MessengerRNA TransportAnimalsFemaleIn Situ Hybridization, FluorescenceMaleMiceRatsRats, Sprague-DawleySpatial AnalysisRNA, MessengermRNA localizationmultiplex imagingneuronsRNA granuleRNP composition

Identifiers

PMID41271436
PMCPMC12700706

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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.