A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization

Summary: Coordinated movement requires the integration of many sensory inputs including proprioception, the sense of relative body position and force associated with movement. Proprioceptive information is relayed to the cerebellum via spinocerebellar neurons, located in the spinal cord within a num...

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Main Authors: Eamon Coughlan, Victoria C. Garside, Siew Fen Lisa Wong, Huazheng Liang, Dominik Kraus, Kajari Karmakar, Upasana Maheshwari, Filippo M. Rijli, James Bourne, Edwina McGlinn
Format: Article
Language:English
Published: Elsevier 2019-11-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124719313622
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spelling doaj-217fc940a6ea405fbe77749caa8e91502020-11-25T01:16:11ZengElsevierCell Reports2211-12472019-11-0129824082421.e4A Hox Code Defines Spinocerebellar Neuron Subtype RegionalizationEamon Coughlan0Victoria C. Garside1Siew Fen Lisa Wong2Huazheng Liang3Dominik Kraus4Kajari Karmakar5Upasana Maheshwari6Filippo M. Rijli7James Bourne8Edwina McGlinn9EMBL Australia, Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, AustraliaEMBL Australia, Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, AustraliaEMBL Australia, Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, AustraliaNeuroscience Research Australia, Randwick, NSW 2031, AustraliaFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland; University of Basel, 4001 Basel, SwitzerlandFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland; University of Basel, 4001 Basel, SwitzerlandFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland; University of Basel, 4001 Basel, SwitzerlandFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland; University of Basel, 4001 Basel, SwitzerlandEMBL Australia, Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, AustraliaEMBL Australia, Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia; Corresponding authorSummary: Coordinated movement requires the integration of many sensory inputs including proprioception, the sense of relative body position and force associated with movement. Proprioceptive information is relayed to the cerebellum via spinocerebellar neurons, located in the spinal cord within a number of major neuronal columns or as various scattered populations. Despite the importance of proprioception to fluid movement, a molecular understanding of spinocerebellar relay interneurons is only beginning to be explored, with limited knowledge of molecular heterogeneity within and between columns. Using fluorescent reporter mice, neuronal tracing, and in situ hybridization, we identify widespread expression of Hox cluster genes within spinocerebellar neurons. We reveal a “Hox code” based on axial level and individual spinocerebellar column, which, at cervico-thoracic levels, is essential for subtype regionalization. Specifically, we show that Hoxc9 function is required in most, but not all, cells of the thoracic spinocerebellar column, Clarke’s column, revealing heterogeneity reliant on Hox signatures. : Coughlan et al. utilize fluorescent reporter mice to characterize the projection patterns of embryonic and adult spinocerebellar neurons (SCNs). Within the spinal cord, axially restricted SCNs are delineated by their unique repertoire of posterior Hox-cluster gene expression, and a requirement for Hox function in SCN subtype regionalization is demonstrated. Keywords: Hox gene, Hox cluster, spinocerebellar, proprioception, sensory neuron, miR-196, Hoxc9, microRNA, Gdnf, spinal cord patterninghttp://www.sciencedirect.com/science/article/pii/S2211124719313622
collection DOAJ
language English
format Article
sources DOAJ
author Eamon Coughlan
Victoria C. Garside
Siew Fen Lisa Wong
Huazheng Liang
Dominik Kraus
Kajari Karmakar
Upasana Maheshwari
Filippo M. Rijli
James Bourne
Edwina McGlinn
spellingShingle Eamon Coughlan
Victoria C. Garside
Siew Fen Lisa Wong
Huazheng Liang
Dominik Kraus
Kajari Karmakar
Upasana Maheshwari
Filippo M. Rijli
James Bourne
Edwina McGlinn
A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
Cell Reports
author_facet Eamon Coughlan
Victoria C. Garside
Siew Fen Lisa Wong
Huazheng Liang
Dominik Kraus
Kajari Karmakar
Upasana Maheshwari
Filippo M. Rijli
James Bourne
Edwina McGlinn
author_sort Eamon Coughlan
title A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
title_short A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
title_full A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
title_fullStr A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
title_full_unstemmed A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization
title_sort hox code defines spinocerebellar neuron subtype regionalization
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2019-11-01
description Summary: Coordinated movement requires the integration of many sensory inputs including proprioception, the sense of relative body position and force associated with movement. Proprioceptive information is relayed to the cerebellum via spinocerebellar neurons, located in the spinal cord within a number of major neuronal columns or as various scattered populations. Despite the importance of proprioception to fluid movement, a molecular understanding of spinocerebellar relay interneurons is only beginning to be explored, with limited knowledge of molecular heterogeneity within and between columns. Using fluorescent reporter mice, neuronal tracing, and in situ hybridization, we identify widespread expression of Hox cluster genes within spinocerebellar neurons. We reveal a “Hox code” based on axial level and individual spinocerebellar column, which, at cervico-thoracic levels, is essential for subtype regionalization. Specifically, we show that Hoxc9 function is required in most, but not all, cells of the thoracic spinocerebellar column, Clarke’s column, revealing heterogeneity reliant on Hox signatures. : Coughlan et al. utilize fluorescent reporter mice to characterize the projection patterns of embryonic and adult spinocerebellar neurons (SCNs). Within the spinal cord, axially restricted SCNs are delineated by their unique repertoire of posterior Hox-cluster gene expression, and a requirement for Hox function in SCN subtype regionalization is demonstrated. Keywords: Hox gene, Hox cluster, spinocerebellar, proprioception, sensory neuron, miR-196, Hoxc9, microRNA, Gdnf, spinal cord patterning
url http://www.sciencedirect.com/science/article/pii/S2211124719313622
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