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Expression of the neurodevelopmental disease susceptibility genes CADM1 and CADM2 in the early human fetal forebrain.

Overview

Authors: Natalie Wucherer1, Maznah Alhesain1,2, Amn Ashhad1, Marc Woodbury‐Smith1,3, Gavin J. Clowry1
ORCID iDs: Gavin J. Clowry
  1. Centre for Neuroscience Newcastle University Biosciences Institute Newcastle Upon Tyne UK
  2. Present address: Department of Anatomy and Histology, College of Medicine Qassim University Buraydah Saudi Arabia
  3. Present address: Division of Developmental Disabilities, Department of Psychiatry Queen's University Kingston Canada
Journal: Journal of anatomy, article 10.1111/joa.70248
Dates: received 4 March 2026; accepted 16 September 2026; published online 10 November 2026; in print November 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1111/joa.70248 · PMID 43010662 · PMCID PMC13752524
Categories: genetics / omics (modality), histology / microscopy (modality), human (organism)
Methods: Smoothing, state filtering, decompositions
Keywords: cell‐adhesion molecules, cerebral cortex, corpus callosum, development, thalamocortical, thalamus
Funding: Wellcome Trust (#099175/Z/12/Z); Medical Research Council (MR/R006237/1, MC/PC/13047)
Citations: not cited yet (Europe PMC); 81 references in the paper

Abstract

CADM1 and CADM2 are cell‐adhesion molecules with likely roles in cell migration, axon guidance and synapse formation. Both are considered potential susceptibility genes for various neurodevelopmental disorders. However, their expression patterns in early human brain development have not been explored. Here we employed transcriptomics, RNAScope in situ hybridisation (ISH) and immunofluorescence (IF) to determine the time course and location of expression in the human cerebral cortex and thalamus between 7.5–17 postconceptional weeks (PCW). In the cerebral cortex, tissue RNAseq revealed both to be highly expressed throughout this period. CADM1 exhibited very high expression which declined slightly with age. CADM2 exhibited high expression which increased over time. Single‐cell RNA‐seq and ISH revealed that both genes were co‐expressed in most cells; however, IF revealed different patterns of cellular localisation. At 8 PCW, expression for both CADMs was similar throughout the cortex and predominantly located in the cytoplasm/cell surface in the cortical plate (CP) but with stronger expression of CADM1 in the subventricular zone. However, from 10 PCW onwards, the strongest immunoreactivity for CADM1 was in the cell nucleus with weak cytoplasmic localisation, whereas CADM2 was expressed on the cell surface and increasingly in axons with age. By 17 PCW, CADM2 exhibited strong immunoreactivity in the thalamocortical and callosal corticocortical axons but was weakly expressed in corticofugal pathways. In the thalamus, CADM2 expression in posterior and lateral projection neurons contributing to thalamocortical pathways was confirmed. CADM1 and CADM2 show differential expression in the thalamus and associated nuclei, suggesting a role in their segregation; CADM1 favouring anterior and medial thalamic nuclei and the ventromedial subthalamus, CADM2 the lateral habenula, lateral and posterior thalamus and dorsolateral subthalamus. CADM1 and CADM2 may play important and varied roles in early fetal human forebrain development, guiding cell migration and aggregation, and axon guidance and fasciculation.

Reproduced under the paper's license (CC BY), from the paper cited above.

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Data availability statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

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Version 1, 12 November 2026: the first record

Recorded: type, language, journal, pages, dates, 5 authors, 6 keywords, 2 funders, 81 references.

Cite

This paper

Wucherer, N., Alhesain, M., Ashhad, A., Woodbury‐Smith, M., & Clowry, G. J. (2026). Expression of the neurodevelopmental disease susceptibility genes CADM1 and CADM2 in the early human fetal forebrain. Journal of anatomy, 10.1111/joa.70248. https://doi.org/10.1111/joa.70248

BibTeX

@article{wucherer2026expression,
author = {Wucherer, Natalie and Alhesain, Maznah and Ashhad, Amn and Woodbury‐Smith, Marc and Clowry, Gavin J.},
title = {{Expression of the neurodevelopmental disease susceptibility genes CADM1 and CADM2 in the early human fetal forebrain}},
journal = {Journal of anatomy},
year = {2026},
month = nov,
pages = {10.1111/joa.70248},
publisher = {Wiley},
issn = {0021-8782},
doi = {10.1111/joa.70248},
url = {https://doi.org/10.1111/joa.70248},
pmid = {43010662},
pmcid = {PMC13752524}
}

RIS

TY - JOUR
AU - Wucherer, Natalie
AU - Alhesain, Maznah
AU - Ashhad, Amn
AU - Woodbury‐Smith, Marc
AU - Clowry, Gavin J.
TI - Expression of the neurodevelopmental disease susceptibility genes CADM1 and CADM2 in the early human fetal forebrain
T2 - Journal of anatomy
J2 - J Anat
PY - 2026
DA - 2026/11/10
SP - 10.1111/joa.70248
SN - 0021-8782
PB - Wiley
DO - 10.1111/joa.70248
UR - https://doi.org/10.1111/joa.70248
LA - en
ER -

CSL-JSON

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