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Transcriptomic encoding of sensorimotor transformation in the midbrain
Sensorimotor transformation, a process that converts sensory stimuli into motor actions, is critical for the brain to initiate behaviors. Although the circuitry involved in sensorimotor transformation has been well delineated, the molecular logic behind this process remains poorly understood. Here,...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341986/ https://www.ncbi.nlm.nih.gov/pubmed/34318750 http://dx.doi.org/10.7554/eLife.69825 |
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author | Xie, Zhiyong Wang, Mengdi Liu, Zeyuan Shang, Congping Zhang, Changjiang Sun, Le Gu, Huating Ran, Gengxin Pei, Qing Ma, Qiang Huang, Meizhu Zhang, Junjing Lin, Rui Zhou, Youtong Zhang, Jiyao Zhao, Miao Luo, Minmin Wu, Qian Cao, Peng Wang, Xiaoqun |
author_facet | Xie, Zhiyong Wang, Mengdi Liu, Zeyuan Shang, Congping Zhang, Changjiang Sun, Le Gu, Huating Ran, Gengxin Pei, Qing Ma, Qiang Huang, Meizhu Zhang, Junjing Lin, Rui Zhou, Youtong Zhang, Jiyao Zhao, Miao Luo, Minmin Wu, Qian Cao, Peng Wang, Xiaoqun |
author_sort | Xie, Zhiyong |
collection | PubMed |
description | Sensorimotor transformation, a process that converts sensory stimuli into motor actions, is critical for the brain to initiate behaviors. Although the circuitry involved in sensorimotor transformation has been well delineated, the molecular logic behind this process remains poorly understood. Here, we performed high-throughput and circuit-specific single-cell transcriptomic analyses of neurons in the superior colliculus (SC), a midbrain structure implicated in early sensorimotor transformation. We found that SC neurons in distinct laminae expressed discrete marker genes. Of particular interest, Cbln2 and Pitx2 were key markers that define glutamatergic projection neurons in the optic nerve (Op) and intermediate gray (InG) layers, respectively. The Cbln2+ neurons responded to visual stimuli mimicking cruising predators, while the Pitx2+ neurons encoded prey-derived vibrissal tactile cues. By forming distinct input and output connections with other brain areas, these neuronal subtypes independently mediated behaviors of predator avoidance and prey capture. Our results reveal that, in the midbrain, sensorimotor transformation for different behaviors may be performed by separate circuit modules that are molecularly defined by distinct transcriptomic codes. |
format | Online Article Text |
id | pubmed-8341986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-83419862021-08-09 Transcriptomic encoding of sensorimotor transformation in the midbrain Xie, Zhiyong Wang, Mengdi Liu, Zeyuan Shang, Congping Zhang, Changjiang Sun, Le Gu, Huating Ran, Gengxin Pei, Qing Ma, Qiang Huang, Meizhu Zhang, Junjing Lin, Rui Zhou, Youtong Zhang, Jiyao Zhao, Miao Luo, Minmin Wu, Qian Cao, Peng Wang, Xiaoqun eLife Neuroscience Sensorimotor transformation, a process that converts sensory stimuli into motor actions, is critical for the brain to initiate behaviors. Although the circuitry involved in sensorimotor transformation has been well delineated, the molecular logic behind this process remains poorly understood. Here, we performed high-throughput and circuit-specific single-cell transcriptomic analyses of neurons in the superior colliculus (SC), a midbrain structure implicated in early sensorimotor transformation. We found that SC neurons in distinct laminae expressed discrete marker genes. Of particular interest, Cbln2 and Pitx2 were key markers that define glutamatergic projection neurons in the optic nerve (Op) and intermediate gray (InG) layers, respectively. The Cbln2+ neurons responded to visual stimuli mimicking cruising predators, while the Pitx2+ neurons encoded prey-derived vibrissal tactile cues. By forming distinct input and output connections with other brain areas, these neuronal subtypes independently mediated behaviors of predator avoidance and prey capture. Our results reveal that, in the midbrain, sensorimotor transformation for different behaviors may be performed by separate circuit modules that are molecularly defined by distinct transcriptomic codes. eLife Sciences Publications, Ltd 2021-07-28 /pmc/articles/PMC8341986/ /pubmed/34318750 http://dx.doi.org/10.7554/eLife.69825 Text en © 2021, Xie et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Xie, Zhiyong Wang, Mengdi Liu, Zeyuan Shang, Congping Zhang, Changjiang Sun, Le Gu, Huating Ran, Gengxin Pei, Qing Ma, Qiang Huang, Meizhu Zhang, Junjing Lin, Rui Zhou, Youtong Zhang, Jiyao Zhao, Miao Luo, Minmin Wu, Qian Cao, Peng Wang, Xiaoqun Transcriptomic encoding of sensorimotor transformation in the midbrain |
title | Transcriptomic encoding of sensorimotor transformation in the midbrain |
title_full | Transcriptomic encoding of sensorimotor transformation in the midbrain |
title_fullStr | Transcriptomic encoding of sensorimotor transformation in the midbrain |
title_full_unstemmed | Transcriptomic encoding of sensorimotor transformation in the midbrain |
title_short | Transcriptomic encoding of sensorimotor transformation in the midbrain |
title_sort | transcriptomic encoding of sensorimotor transformation in the midbrain |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341986/ https://www.ncbi.nlm.nih.gov/pubmed/34318750 http://dx.doi.org/10.7554/eLife.69825 |
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