Evidence map›Paper›PMID 25615592›Full record

ArticlePLoS computational biology2015

Laminar and dorsoventral molecular organization of the medial entorhinal cortex revealed by large-scale anatomical analysis of gene expression.

Helen L Ramsden, Gülşen Sürmeli, Steven G McDonagh, Matthew F Nolan

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
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

29 citing papers in PubMed, 57 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2025
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  4. T-type CaCell reports · 2023
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  14. Resurgent Sodium Current in Neurons of the Cerebral Cortex.Frontiers in cellular neuroscience · 2021
    Article
  15. Article
  16. Article
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  18. Electrophysiological and Molecular Characterization of the Parasubiculum.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  19. Review
  20. Review
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 at 2 institutions in 2 countries.

Helen L RamsdenCentre for Integrative Physiology, University of Edinburgh, Edinburgh, United Kingdom; Neuroinformatics Doctoral Training Centre, School of Informatics, University of Edinburgh, Edinburgh, United Kingdom.
Gülşen SürmeliCentre for Integrative Physiology, University of Edinburgh, Edinburgh, United Kingdom.
Steven G McDonaghInstitute of Perception, Action and Behaviour, School of Informatics, University of Edinburgh, Edinburgh, United Kingdom.
Matthew F NolanCentre for Integrative Physiology, University of Edinburgh, Edinburgh, United Kingdom; Centre for Brain Development and Repair, inStem, Bangalore, India.
University of Edinburgh · GBInstitute for Stem Cell Biology and Regenerative Medicine · IN

Funding

Biotechnology and Biological Sciences Research Council BB/1022147/1Biotechnology and Biological Sciences Research Council BB/L010496/1Wellcome TrustWellcome Trust 098915/Z/12/Z
6 · The paper itself

Abstract

Neural circuits in the medial entorhinal cortex (MEC) encode an animal's position and orientation in space. Within the MEC spatial representations, including grid and directional firing fields, have a laminar and dorsoventral organization that corresponds to a similar topography of neuronal connectivity and cellular properties. Yet, in part due to the challenges of integrating anatomical data at the resolution of cortical layers and borders, we know little about the molecular components underlying this organization. To address this we develop a new computational pipeline for high-throughput analysis and comparison of in situ hybridization (ISH) images at laminar resolution. We apply this pipeline to ISH data for over 16,000 genes in the Allen Brain Atlas and validate our analysis with RNA sequencing of MEC tissue from adult mice. We find that differential gene expression delineates the borders of the MEC with neighboring brain structures and reveals its laminar and dorsoventral organization. We propose a new molecular basis for distinguishing the deep layers of the MEC and show that their similarity to corresponding layers of neocortex is greater than that of superficial layers. Our analysis identifies ion channel-, cell adhesion- and synapse-related genes as candidates for functional differentiation of MEC layers and for encoding of spatial information at different scales along the dorsoventral axis of the MEC. We also reveal laminar organization of genes related to disease pathology and suggest that a high metabolic demand predisposes layer II to neurodegenerative pathology. In principle, our computational pipeline can be applied to high-throughput analysis of many forms of neuroanatomical data. Our results support the hypothesis that differences in gene expression contribute to functional specialization of superficial layers of the MEC and dorsoventral organization of the scale of spatial representations.

Indexed as

AnimalsEntorhinal CortexGene Expression ProfilingImage Processing, Computer-AssistedMaleMiceMice, Inbred C57BLMolecular ImagingOrgan Specificity

Identifiers

PMID25615592
PMCPMC4304787
OpenAlexW2049033529

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.