Muscle-selective RUNX3 dependence of sensorimotor circuit development

Author:

Wang Yiqiao1,Wu Haohao1,Zelenin Pavel1,Fontanet Paula1,Wanderoy Simone1,Petitpré Charles1,Comai Glenda2,Bellardita Carmelo3,Xue-Franzén Yongtao1,Huettl Rosa-Eva4,Huber Brosamle Andrea4,Tajbakhsh Shahragim2,Kiehn Ole13,Ernfors Patrik5,Deliagina Tatiana G.1,Lallemend François16,Hadjab Saida1ORCID

Affiliation:

1. Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden

2. Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France

3. Department of Neuroscience, University of Copenhagen, Copenhagen, Denmark

4. Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Developmental Genetics, Neuherberg, Germany

5. Unit of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden

6. Ming Wai Lau Centre for Reparative Medicine, Stockholm node, Karolinska Institutet, Stockholm, Sweden

Abstract

The control of all our motor outputs requires constant monitoring by proprioceptive sensory neurons (PSNs) that convey continuous muscle sensory inputs to the spinal motor network. Yet, the molecular programs that control the establishment of this sensorimotor circuit remain largely unknown. The transcription factor RUNX3 is essential for the early steps of PSNs differentiation, making it difficult to study its role during later aspects of PSNs specification. Here, we conditionally inactivate Runx3 in PSNs after peripheral innervation and identify that RUNX3 is necessary for maintenance of cell identity of only a subgroup of PSNs, without discernable cell death. RUNX3 controls also the sensorimotor connection between PSNs and motor neurons at limb level, with muscle-by-muscle variable sensitivities to the loss of Runx3 that correlate with levels of RUNX3 in PSNs. Finally, we find that muscles and neurotrophin-3 signaling are necessary for maintenance of RUNX3 expression in PSNs. Hence, a transcriptional regulator critical for specifying a generic PSN type identity after neurogenesis, is later regulated by target muscle-derived signal to contribute to the specialized aspects of the sensorimotor connection selectivity.

Funder

Karolinska Institutet

Vetenskapsrådet

Knut och Alice Wallenbergs Stiftelse

Ragnar Söderbergs stiftelse

Ming Wai Lau grant

StratNeuro

Hjärnfonden

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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