Transcriptomic encoding of sensorimotor transformation in the midbrain

Author:

Xie Zhiyong1ORCID,Wang Mengdi23ORCID,Liu Zeyuan23ORCID,Shang Congping4,Zhang Changjiang23,Sun Le5,Gu Huating1,Ran Gengxin23,Pei Qing1,Ma Qiang23,Huang Meizhu4,Zhang Junjing6,Lin Rui1,Zhou Youtong1,Zhang Jiyao6,Zhao Miao1,Luo Minmin17ORCID,Wu Qian6ORCID,Cao Peng18ORCID,Wang Xiaoqun23457ORCID

Affiliation:

1. National Institute of Biological Sciences, Beijing, China

2. State Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology (Shanghai), Institute of Biophysics, Chinese Academy of Sciences, Beijing, China

3. University of Chinese Academy of Sciences, Beijing, China

4. Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory), Guangzhou, China

5. Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China

6. State Key Laboratory of Cognitive Neuroscience and Learning, IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China

7. Chinese Institute for Brain Research, Beijing, China

8. Tsinghua Institute of Multidisciplinary Biomedical Research, Tsinghua University, Beijing, China

Abstract

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.

Funder

Ministry of Science and Technology of the People's Republic of China

Chinese Academy of Sciences

National Natural Science Foundation of China

BUAA-CCMU Big Data and Precision Medicine Advanced Innovation Center Project

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference96 articles.

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