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CaMKII mediates sexually dimorphic synaptic transmission at neuromuscular junctions in C. elegans.
Zeng, Wan-Xin; Liu, Haowen; Hao, Yue; Qian, Kang-Ying; Tian, Fu-Min; Li, Lei; Yu, Bin; Zeng, Xian-Ting; Gao, Shangbang; Hu, Zhitao; Tong, Xia-Jing.
Afiliação
  • Zeng WX; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
  • Liu H; Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences , Shanghai, China.
  • Hao Y; University of Chinese Academy of Sciences , Beijing, China.
  • Qian KY; Queensland Brain Institute, Clem Jones Centre for Ageing Dementia Research (CJCADR), The University of Queensland , Brisbane, Australia.
  • Tian FM; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
  • Li L; Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences , Shanghai, China.
  • Yu B; University of Chinese Academy of Sciences , Beijing, China.
  • Zeng XT; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
  • Gao S; Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences , Shanghai, China.
  • Hu Z; University of Chinese Academy of Sciences , Beijing, China.
  • Tong XJ; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
J Cell Biol ; 222(11)2023 11 06.
Article em En | MEDLINE | ID: mdl-37624117
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Caenorhabditis elegans / Transmissão Sináptica / Proteínas de Caenorhabditis elegans / Proteína Quinase Tipo 2 Dependente de Cálcio-Calmodulina / Junção Neuromuscular Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Caenorhabditis elegans / Transmissão Sináptica / Proteínas de Caenorhabditis elegans / Proteína Quinase Tipo 2 Dependente de Cálcio-Calmodulina / Junção Neuromuscular Idioma: En Ano de publicação: 2023 Tipo de documento: Article