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Polycomb group genes are required for neuronal pruning in Drosophila
BACKGROUND: Pruning that selectively eliminates unnecessary or incorrect neurites is required for proper wiring of the mature nervous system. During Drosophila metamorphosis, dendritic arbourization sensory neurons (ddaCs) and mushroom body (MB) γ neurons can selectively prune their larval dendrites...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933400/ https://www.ncbi.nlm.nih.gov/pubmed/36793038 http://dx.doi.org/10.1186/s12915-023-01534-0 |
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author | Bu, Shufeng Lau, Samuel Song Yuan Yong, Wei Lin Zhang, Heng Thiagarajan, Sasinthiran Bashirullah, Arash Yu, Fengwei |
author_facet | Bu, Shufeng Lau, Samuel Song Yuan Yong, Wei Lin Zhang, Heng Thiagarajan, Sasinthiran Bashirullah, Arash Yu, Fengwei |
author_sort | Bu, Shufeng |
collection | PubMed |
description | BACKGROUND: Pruning that selectively eliminates unnecessary or incorrect neurites is required for proper wiring of the mature nervous system. During Drosophila metamorphosis, dendritic arbourization sensory neurons (ddaCs) and mushroom body (MB) γ neurons can selectively prune their larval dendrites and/or axons in response to the steroid hormone ecdysone. An ecdysone-induced transcriptional cascade plays a key role in initiating neuronal pruning. However, how downstream components of ecdysone signalling are induced remains not entirely understood. RESULTS: Here, we identify that Scm, a component of Polycomb group (PcG) complexes, is required for dendrite pruning of ddaC neurons. We show that two PcG complexes, PRC1 and PRC2, are important for dendrite pruning. Interestingly, depletion of PRC1 strongly enhances ectopic expression of Abdominal B (Abd-B) and Sex combs reduced, whereas loss of PRC2 causes mild upregulation of Ultrabithorax and Abdominal A in ddaC neurons. Among these Hox genes, overexpression of Abd-B causes the most severe pruning defects, suggesting its dominant effect. Knockdown of the core PRC1 component Polyhomeotic (Ph) or Abd-B overexpression selectively downregulates Mical expression, thereby inhibiting ecdysone signalling. Finally, Ph is also required for axon pruning and Abd-B silencing in MB γ neurons, indicating a conserved function of PRC1 in two types of pruning. CONCLUSIONS: This study demonstrates important roles of PcG and Hox genes in regulating ecdysone signalling and neuronal pruning in Drosophila. Moreover, our findings suggest a non-canonical and PRC2-independent role of PRC1 in Hox gene silencing during neuronal pruning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01534-0. |
format | Online Article Text |
id | pubmed-9933400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99334002023-02-17 Polycomb group genes are required for neuronal pruning in Drosophila Bu, Shufeng Lau, Samuel Song Yuan Yong, Wei Lin Zhang, Heng Thiagarajan, Sasinthiran Bashirullah, Arash Yu, Fengwei BMC Biol Research Article BACKGROUND: Pruning that selectively eliminates unnecessary or incorrect neurites is required for proper wiring of the mature nervous system. During Drosophila metamorphosis, dendritic arbourization sensory neurons (ddaCs) and mushroom body (MB) γ neurons can selectively prune their larval dendrites and/or axons in response to the steroid hormone ecdysone. An ecdysone-induced transcriptional cascade plays a key role in initiating neuronal pruning. However, how downstream components of ecdysone signalling are induced remains not entirely understood. RESULTS: Here, we identify that Scm, a component of Polycomb group (PcG) complexes, is required for dendrite pruning of ddaC neurons. We show that two PcG complexes, PRC1 and PRC2, are important for dendrite pruning. Interestingly, depletion of PRC1 strongly enhances ectopic expression of Abdominal B (Abd-B) and Sex combs reduced, whereas loss of PRC2 causes mild upregulation of Ultrabithorax and Abdominal A in ddaC neurons. Among these Hox genes, overexpression of Abd-B causes the most severe pruning defects, suggesting its dominant effect. Knockdown of the core PRC1 component Polyhomeotic (Ph) or Abd-B overexpression selectively downregulates Mical expression, thereby inhibiting ecdysone signalling. Finally, Ph is also required for axon pruning and Abd-B silencing in MB γ neurons, indicating a conserved function of PRC1 in two types of pruning. CONCLUSIONS: This study demonstrates important roles of PcG and Hox genes in regulating ecdysone signalling and neuronal pruning in Drosophila. Moreover, our findings suggest a non-canonical and PRC2-independent role of PRC1 in Hox gene silencing during neuronal pruning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01534-0. BioMed Central 2023-02-15 /pmc/articles/PMC9933400/ /pubmed/36793038 http://dx.doi.org/10.1186/s12915-023-01534-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Bu, Shufeng Lau, Samuel Song Yuan Yong, Wei Lin Zhang, Heng Thiagarajan, Sasinthiran Bashirullah, Arash Yu, Fengwei Polycomb group genes are required for neuronal pruning in Drosophila |
title | Polycomb group genes are required for neuronal pruning in Drosophila |
title_full | Polycomb group genes are required for neuronal pruning in Drosophila |
title_fullStr | Polycomb group genes are required for neuronal pruning in Drosophila |
title_full_unstemmed | Polycomb group genes are required for neuronal pruning in Drosophila |
title_short | Polycomb group genes are required for neuronal pruning in Drosophila |
title_sort | polycomb group genes are required for neuronal pruning in drosophila |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933400/ https://www.ncbi.nlm.nih.gov/pubmed/36793038 http://dx.doi.org/10.1186/s12915-023-01534-0 |
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