The neural circuits governing behaviors vital to mammals, such as locomotion and respiration, rely on the ability of motor neurons (MNs) to establish selective connections with target cells both centrally and peripherally. Motor neurons innervating specific muscle targets are specified by the large family of chromosomally arrayed Hox transcription factors. A key aspect of Hox gene function is to segregate motor neurons into topographically organized columnar and pool subtypes. While it has been suggested the somatotopic organization of MNs evolved to facilitate the activation of an increasingly more complex limb musculature, it is largely unknown how MNs cluster into columns, and what role MN position plays in shaping the specificity of connections within motor networks. In this proposal we will investigate the function of Pbx genes, essential co-factors of Hox proteins, in the formation of MN topographic maps and in the development of motor circuits. The major goals of this proposal are to: 1) to assess the role of Pbx genes in the organization and connectivity of spinal motor neurons, 2) to determine the mechanisms through which motor neurons are topographically organized, and 3) to define the role of MN position and identity in spinal circuit assembly.
In Aim1 we will define the function of Pbx genes in MN differentiation using genetic manipulations and histological assays.
In Aim2 we will identity the targets of Pbx proteins in MNs, and assess their function and mechanisms of regulation.
In Aim3 we will assess how motor neuron position and identity influences the specificity of connections with presynaptic interneuron populations. By building off our in depth knowledge of motor neuron specification programs in mammals, these studies should provide basic insights into the mechanisms through which motor circuits are assembled.

Public Health Relevance

A major goal in the neurosciences has been to understand how neuronal cell types are specified during development, and to resolve how subtype identity contributes to the specificity of connections within neural circuits. The overall goal of this proposal is to elucidate the genetic mechanisms that define the ability of motor neuron subtypes to organize into columns and connect with the spinal networks that control walking and breathing. Defining the mechanisms underlying the construction of spinal circuits should provide basic insights relevant to the study of diseases and injuries of the spinal cord that affect motor function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS097550-02
Application #
9281061
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Lavaute, Timothy M
Project Start
2016-07-01
Project End
2021-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
2
Fiscal Year
2017
Total Cost
$333,702
Indirect Cost
$136,827
Name
New York University
Department
Neurology
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
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D'Elia, Kristen P; Dasen, Jeremy S (2018) Development, functional organization, and evolution of vertebrate axial motor circuits. Neural Dev 13:10
Baek, Myungin; Pivetta, Chiara; Liu, Jeh-Ping et al. (2017) Columnar-Intrinsic Cues Shape Premotor Input Specificity in Locomotor Circuits. Cell Rep 21:867-877
Dasen, Jeremy S (2017) Master or servant? emerging roles for motor neuron subtypes in the construction and evolution of locomotor circuits. Curr Opin Neurobiol 42:25-32
Hanley, Olivia; Zewdu, Rediet; Cohen, Lisa J et al. (2016) Parallel Pbx-Dependent Pathways Govern the Coalescence and Fate of Motor Columns. Neuron 91:1005-1020