Motor neuron position and topographic order imposed by β- And γ-catenin activities
Open accessAbstract
Neurons typically settle at positions that match the location of their synaptic targets, creating topographic maps. In the spinal cord, the organization of motor neurons into discrete clusters is linked to the location of their muscle targets, establishing a topographic map of punctate design. To define the significance of motor pool organization for neuromuscular map formation, we assessed the role of cadherin-catenin signaling in motor neuron positioning and limb muscle innervation. We find that joint inactivation of β- and γ-catenin scrambles motor neuron settling position in the spinal cord but fails to erode the predictive link between motor neuron transcriptional identity and muscle target. Inactivation of N-cadherin perturbs pool positioning in similar ways, albeit with reduced penetrance. These findings reveal that cadherin-catenin signaling directs motor pool patterning and imposes topographic order on an underlying identity-based neural map.
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Differential cell adhesion is essential for the clustering of MNs into distinct pools in the spinal cord.
“In the spinal cord, differential cell adhesion is essential for the clustering of MNs into distinct pools”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Demireva et al., 2011
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References 52 · Cited by 85
- Authors
- Demireva, E. Y., Shapiro, L. S., Jessell, T. M., & Zampieri, N.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Jessell, Thomas M.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2011-10
- Volume
- 147
- Issue
- 3
- Pages
- 641-652
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3226777
- OpenAlex
- W1985961137
- Cited by
- 85
- References
- 52
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 1 · 2023: 1 · 2022: 6 · 2021: 2 · 2020: 9 · 2019: 6 · 2018: 5 · 2017: 8 · 2016: 7 · 2015: 11 · 2014: 7 · 2013: 5 · 2012: 8
- FWCI
- 2.85
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 691 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Wellcome Trust
- National Institute of General Medical Sciences (R01GM062270)
- National Institute of Neurological Disorders and Stroke (R37NS033245, R01NS033245)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- topographic map, β-catenin, gamma-catenin, N-cadherin, spinal motoneurons, muscle innervation
- MeSH terms
- Animals, Embryo, Mammalian, Biological Evolution, Motor Neurons, Mutation, Spinal Cord, Signal Transduction, Cadherins, Body Patterning, beta Catenin, gamma Catenin, Mice, Wnt Signaling Pathway
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