Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction

Neuroligins are postsynaptic adhesion molecules that are essential for postsynaptic specialization and synaptic function. But the underlying molecular mechanisms of neuroligin functions remain unclear. We found that Drosophila Neuroligin 1 (DNlg1) regulates synaptic structure and function through WA...

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Main Authors: Guanglin Xing, Moyi Li, Yichen Sun, Menglong Rui, Yan Zhuang, Huihui Lv, Junhai Han, Zhengping Jia, Wei Xie
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-03-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/30457
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spelling doaj-646643a9036347eabc32dac5f03379ea2021-05-05T15:43:44ZengeLife Sciences Publications LtdeLife2050-084X2018-03-01710.7554/eLife.30457Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junctionGuanglin Xing0https://orcid.org/0000-0002-8258-0293Moyi Li1https://orcid.org/0000-0003-3566-3931Yichen Sun2Menglong Rui3Yan Zhuang4Huihui Lv5Junhai Han6https://orcid.org/0000-0001-8941-2578Zhengping Jia7https://orcid.org/0000-0003-4413-5364Wei Xie8https://orcid.org/0000-0002-9179-4787Institute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, China; The Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China; Co-innovation Center of Neuroregeneration, Nantong University, Nantong, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, ChinaThe Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, China; The Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China; Co-innovation Center of Neuroregeneration, Nantong University, Nantong, ChinaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, China; Neurosciences and Mental Health Program, The Hospital for Sick Children, University of Toronto, Ontario, CanadaInstitute of Life Sciences, the Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, China; The Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China; Co-innovation Center of Neuroregeneration, Nantong University, Nantong, ChinaNeuroligins are postsynaptic adhesion molecules that are essential for postsynaptic specialization and synaptic function. But the underlying molecular mechanisms of neuroligin functions remain unclear. We found that Drosophila Neuroligin 1 (DNlg1) regulates synaptic structure and function through WAVE regulatory complex (WRC)-mediated postsynaptic actin reorganization. The disruption of DNlg1, DNlg2, or their presynaptic partner neurexin (DNrx) led to a dramatic decrease in the amount of F-actin. Further study showed that DNlg1, but not DNlg2 or DNlg3, directly interacts with the WRC via its C-terminal interacting receptor sequence. That interaction is required to recruit WRC to the postsynaptic membrane to promote F-actin assembly. Furthermore, the interaction between DNlg1 and the WRC is essential for DNlg1 to rescue the morphological and electrophysiological defects in dnlg1 mutants. Our results reveal a novel mechanism by which the DNrx-DNlg1 trans-synaptic interaction coordinates structural and functional properties at the neuromuscular junction.https://elifesciences.org/articles/30457NeuroliginWAVE regulatory complexpostsynaptic assemblyF-actinsynapse
collection DOAJ
language English
format Article
sources DOAJ
author Guanglin Xing
Moyi Li
Yichen Sun
Menglong Rui
Yan Zhuang
Huihui Lv
Junhai Han
Zhengping Jia
Wei Xie
spellingShingle Guanglin Xing
Moyi Li
Yichen Sun
Menglong Rui
Yan Zhuang
Huihui Lv
Junhai Han
Zhengping Jia
Wei Xie
Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
eLife
Neuroligin
WAVE regulatory complex
postsynaptic assembly
F-actin
synapse
author_facet Guanglin Xing
Moyi Li
Yichen Sun
Menglong Rui
Yan Zhuang
Huihui Lv
Junhai Han
Zhengping Jia
Wei Xie
author_sort Guanglin Xing
title Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
title_short Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
title_full Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
title_fullStr Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
title_full_unstemmed Neurexin–Neuroligin 1 regulates synaptic morphology and functions via the WAVE regulatory complex in Drosophila neuromuscular junction
title_sort neurexin–neuroligin 1 regulates synaptic morphology and functions via the wave regulatory complex in drosophila neuromuscular junction
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-03-01
description Neuroligins are postsynaptic adhesion molecules that are essential for postsynaptic specialization and synaptic function. But the underlying molecular mechanisms of neuroligin functions remain unclear. We found that Drosophila Neuroligin 1 (DNlg1) regulates synaptic structure and function through WAVE regulatory complex (WRC)-mediated postsynaptic actin reorganization. The disruption of DNlg1, DNlg2, or their presynaptic partner neurexin (DNrx) led to a dramatic decrease in the amount of F-actin. Further study showed that DNlg1, but not DNlg2 or DNlg3, directly interacts with the WRC via its C-terminal interacting receptor sequence. That interaction is required to recruit WRC to the postsynaptic membrane to promote F-actin assembly. Furthermore, the interaction between DNlg1 and the WRC is essential for DNlg1 to rescue the morphological and electrophysiological defects in dnlg1 mutants. Our results reveal a novel mechanism by which the DNrx-DNlg1 trans-synaptic interaction coordinates structural and functional properties at the neuromuscular junction.
topic Neuroligin
WAVE regulatory complex
postsynaptic assembly
F-actin
synapse
url https://elifesciences.org/articles/30457
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