CaMKII mediates sexually dimorphic synaptic transmission at neuromuscular junctions in C. elegans

Author:

Zeng Wan-Xin123ORCID,Liu Haowen4ORCID,Hao Yue123ORCID,Qian Kang-Ying123ORCID,Tian Fu-Min1ORCID,Li Lei4ORCID,Yu Bin5ORCID,Zeng Xian-Ting1ORCID,Gao Shangbang5ORCID,Hu Zhitao46ORCID,Tong Xia-Jing1ORCID

Affiliation:

1. ShanghaiTech University 1 School of Life Science and Technology, , Shanghai, China

2. Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences 2 , Shanghai, China

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

4. Queensland Brain Institute, Clem Jones Centre for Ageing Dementia Research (CJCADR), The University of Queensland 4 , Brisbane, Australia

5. College of Life Science and Technology, Huazhong University of Science and Technology 5 , Wuhan, China

6. City University of Hong Kong 6 Department of Neuroscience, , Kowloon, China

Abstract

Sexually dimorphic behaviors are ubiquitous throughout the animal kingdom. Although both sex-specific and sex-shared neurons have been functionally implicated in these diverse behaviors, less is known about the roles of sex-shared neurons. Here, we discovered sexually dimorphic cholinergic synaptic transmission in C. elegans occurring at neuromuscular junctions (NMJs), with males exhibiting increased release frequencies, which result in sexually dimorphic locomotion behaviors. Scanning electron microscopy revealed that males have significantly more synaptic vesicles (SVs) at their cholinergic synapses than hermaphrodites. Analysis of previously published transcriptome identified the male-enriched transcripts and focused our attention on UNC-43/CaMKII. We ultimately show that differential accumulation of UNC-43 at cholinergic neurons controls axonal SV abundance and synaptic transmission. Finally, we demonstrate that sex reversal of all neurons in hermaphrodites generates male-like cholinergic transmission and locomotion behaviors. Thus, beyond demonstrating UNC-43/CaMKII as an essential mediator of sex-specific synaptic transmission, our study provides molecular and cellular insights into how sex-shared neurons can generate sexually dimorphic locomotion behaviors.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

National Health and Medical Research Council

Science and Technology Commission of Shanghai Municipality

Publisher

Rockefeller University Press

Subject

Cell Biology

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