The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography

Abstract The topographic projection of afferent terminals into two-dimensional maps is essential for sensory systems to encode the locations of sensory stimuli. In vertebrates, guidance cues are critical for establishing a coarse topographic map, while neuronal activity directs fine-scale topography...

Full description

Bibliographic Details
Main Authors: Ruonan Li, Yuhua Liang, Siyang Zheng, Qun He, Limin Yang
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Molecular Brain
Subjects:
Online Access:https://doi.org/10.1186/s13041-019-0531-7
id doaj-36fa3ce51a0d4a889d29c58ea9c9bb4c
record_format Article
spelling doaj-36fa3ce51a0d4a889d29c58ea9c9bb4c2020-12-13T12:20:54ZengBMCMolecular Brain1756-66062019-12-011211810.1186/s13041-019-0531-7The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topographyRuonan Li0Yuhua Liang1Siyang Zheng2Qun He3Limin Yang4School of Medicine, Dalian UniversitySchool of Medicine, Dalian UniversityLife Sciences Institute, Dalian National UniversitySchool of Medicine, Dalian UniversitySchool of Medicine, Dalian UniversityAbstract The topographic projection of afferent terminals into two-dimensional maps is essential for sensory systems to encode the locations of sensory stimuli. In vertebrates, guidance cues are critical for establishing a coarse topographic map, while neuronal activity directs fine-scale topography between adjacent afferent terminals. However, the molecular mechanism underlying activity-dependent fine-scale topography is not well known. Studies in the Drosophila visual system have demonstrated that cell-adhesion molecules direct fine-scale topography, but whether or not these molecules are involved in activity-dependent fine-scale topography remains to be determined. We previously reported that the nociceptors in Drosophila larvae form an activity-dependent fine-scale topographic system. The establishment of this system is instructed by the level of neuronal activity in individual nociceptors. Here, we show that the atypical cadherin Flamingo (Fmi) is required for establishing the nociceptor topographic map. We found that the topographic defect caused by loss of fmi was epistatic to the inhibition of neuronal activity and the overexpression of the activity-regulated gene Trim9. These results suggest that Fmi and neuronal activity interact to regulate fine-scale topography. This study provides a link between neuronal activity and the cell-adhesion molecule in the establishment of fine-scale topography.https://doi.org/10.1186/s13041-019-0531-7Fine-scale topographyFlamingoNeuronal activityCompetenceDrosophilaCell-adhesion molecule
collection DOAJ
language English
format Article
sources DOAJ
author Ruonan Li
Yuhua Liang
Siyang Zheng
Qun He
Limin Yang
spellingShingle Ruonan Li
Yuhua Liang
Siyang Zheng
Qun He
Limin Yang
The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
Molecular Brain
Fine-scale topography
Flamingo
Neuronal activity
Competence
Drosophila
Cell-adhesion molecule
author_facet Ruonan Li
Yuhua Liang
Siyang Zheng
Qun He
Limin Yang
author_sort Ruonan Li
title The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
title_short The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
title_full The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
title_fullStr The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
title_full_unstemmed The atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
title_sort atypical cadherin flamingo determines the competence of neurons for activity-dependent fine-scale topography
publisher BMC
series Molecular Brain
issn 1756-6606
publishDate 2019-12-01
description Abstract The topographic projection of afferent terminals into two-dimensional maps is essential for sensory systems to encode the locations of sensory stimuli. In vertebrates, guidance cues are critical for establishing a coarse topographic map, while neuronal activity directs fine-scale topography between adjacent afferent terminals. However, the molecular mechanism underlying activity-dependent fine-scale topography is not well known. Studies in the Drosophila visual system have demonstrated that cell-adhesion molecules direct fine-scale topography, but whether or not these molecules are involved in activity-dependent fine-scale topography remains to be determined. We previously reported that the nociceptors in Drosophila larvae form an activity-dependent fine-scale topographic system. The establishment of this system is instructed by the level of neuronal activity in individual nociceptors. Here, we show that the atypical cadherin Flamingo (Fmi) is required for establishing the nociceptor topographic map. We found that the topographic defect caused by loss of fmi was epistatic to the inhibition of neuronal activity and the overexpression of the activity-regulated gene Trim9. These results suggest that Fmi and neuronal activity interact to regulate fine-scale topography. This study provides a link between neuronal activity and the cell-adhesion molecule in the establishment of fine-scale topography.
topic Fine-scale topography
Flamingo
Neuronal activity
Competence
Drosophila
Cell-adhesion molecule
url https://doi.org/10.1186/s13041-019-0531-7
work_keys_str_mv AT ruonanli theatypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT yuhualiang theatypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT siyangzheng theatypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT qunhe theatypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT liminyang theatypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT ruonanli atypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT yuhualiang atypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT siyangzheng atypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT qunhe atypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
AT liminyang atypicalcadherinflamingodeterminesthecompetenceofneuronsforactivitydependentfinescaletopography
_version_ 1724384869940723712