TY - JOUR
T1 - Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization
AU - Goldblatt, Dena
AU - Huang, Stephanie
AU - Greaney, Marie R.
AU - Hamling, Kyla R.
AU - Voleti, Venkatakaushik
AU - Perez-Campos, Citlali
AU - Patel, Kripa B.
AU - Li, Wenze
AU - Hillman, Elizabeth M.C.
AU - Bagnall, Martha W.
AU - Schoppik, David
N1 - Publisher Copyright:
© 2023 The Author(s)
PY - 2023/4/10
Y1 - 2023/4/10
N2 - Across the nervous system, neurons with similar attributes are topographically organized. This topography reflects developmental pressures. Oddly, vestibular (balance) nuclei are thought to be disorganized. By measuring activity in birthdated neurons, we revealed a functional map within the central vestibular projection nucleus that stabilizes gaze in the larval zebrafish. We first discovered that both somatic position and stimulus selectivity follow projection neuron birthdate. Next, with electron microscopy and loss-of-function assays, we found that patterns of peripheral innervation to projection neurons were similarly organized by birthdate. Finally, birthdate revealed spatial patterns of axonal arborization and synapse formation to projection neuron outputs. Collectively, we find that development reveals previously hidden organization to the input, processing, and output layers of a highly conserved vertebrate sensorimotor circuit. The spatial and temporal attributes we uncover constrain the developmental mechanisms that may specify the fate, function, and organization of vestibulo-ocular reflex neurons. More broadly, our data suggest that, like invertebrates, temporal mechanisms may assemble vertebrate sensorimotor architecture.
AB - Across the nervous system, neurons with similar attributes are topographically organized. This topography reflects developmental pressures. Oddly, vestibular (balance) nuclei are thought to be disorganized. By measuring activity in birthdated neurons, we revealed a functional map within the central vestibular projection nucleus that stabilizes gaze in the larval zebrafish. We first discovered that both somatic position and stimulus selectivity follow projection neuron birthdate. Next, with electron microscopy and loss-of-function assays, we found that patterns of peripheral innervation to projection neurons were similarly organized by birthdate. Finally, birthdate revealed spatial patterns of axonal arborization and synapse formation to projection neuron outputs. Collectively, we find that development reveals previously hidden organization to the input, processing, and output layers of a highly conserved vertebrate sensorimotor circuit. The spatial and temporal attributes we uncover constrain the developmental mechanisms that may specify the fate, function, and organization of vestibulo-ocular reflex neurons. More broadly, our data suggest that, like invertebrates, temporal mechanisms may assemble vertebrate sensorimotor architecture.
KW - circuit assembly
KW - development
KW - topography
KW - vestibular
KW - zebrafish
UR - http://www.scopus.com/inward/record.url?scp=85151538489&partnerID=8YFLogxK
U2 - 10.1016/j.cub.2023.02.048
DO - 10.1016/j.cub.2023.02.048
M3 - Article
C2 - 36924768
AN - SCOPUS:85151538489
SN - 0960-9822
VL - 33
SP - 1265-1281.e7
JO - Current Biology
JF - Current Biology
IS - 7
ER -