Cargando…
The H3K27 demethylase controls the lateral line embryogenesis of zebrafish
BACKGROUND: Kdm6b, a specific histone 3 lysine 27 (H3K27) demethylase, has been reported to be implicated in a variety of developmental processes including cell differentiation and cell fate determination and multiple organogenesis. Here, we regulated the transcript level of kdm6bb to study the pote...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406677/ https://www.ncbi.nlm.nih.gov/pubmed/34716527 http://dx.doi.org/10.1007/s10565-021-09669-y |
_version_ | 1785085796820189184 |
---|---|
author | Tang, Dongmei Lu, Yitong Zuo, Na Yan, Renchun Wu, Cheng Wu, Lijuan Liu, Shaofeng He, Yingzi |
author_facet | Tang, Dongmei Lu, Yitong Zuo, Na Yan, Renchun Wu, Cheng Wu, Lijuan Liu, Shaofeng He, Yingzi |
author_sort | Tang, Dongmei |
collection | PubMed |
description | BACKGROUND: Kdm6b, a specific histone 3 lysine 27 (H3K27) demethylase, has been reported to be implicated in a variety of developmental processes including cell differentiation and cell fate determination and multiple organogenesis. Here, we regulated the transcript level of kdm6bb to study the potential role in controlling the hearing organ development of zebrafish. METHODS: A morpholino antisense oligonucleotide (MO) strategy was used to induce Kdm6b deficiency; immunohistochemical staining and in situ hybridization analysis were conducted to figure out the morphologic alterations and embryonic mechanisms. RESULTS: Kdm6bb is expressed in the primordium and neuromasts at the early stage of zebrafish embryogenesis, suggesting a potential function of Kdm6b in the development of mechanosensory organs. Knockdown of kdm6bb severely influences the cell migration and proliferation in posterior lateral line primordium, abates the number of neuromasts along the trunk, and mRNA-mediated rescue test can partially renew the neuromasts. Loss of kdm6bb might be related to aberrant expressions of chemokine genes encompassing cxcl12a and cxcr4b/cxcr7b in the migrating primordium. Moreover, inhibition of kdm6bb reduces the expression of genes in Fgf signaling pathway, while it increases the axin2 and lef1 expression level of Wnt/β-catenin signaling during the migrating stage. CONCLUSIONS: Collectively, our results revealed that Kdm6b plays an essential role in guiding the migration of primordium and in regulating the deposition of zebrafish neuromasts by mediating the gene expression of chemokines and Wnt and Fgf signaling pathway. Since histone methylation and demethylation are reversible, targeting Kdm6b may present as a novel therapeutic regimen for hearing disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-021-09669-y. |
format | Online Article Text |
id | pubmed-10406677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-104066772023-08-09 The H3K27 demethylase controls the lateral line embryogenesis of zebrafish Tang, Dongmei Lu, Yitong Zuo, Na Yan, Renchun Wu, Cheng Wu, Lijuan Liu, Shaofeng He, Yingzi Cell Biol Toxicol Original Article BACKGROUND: Kdm6b, a specific histone 3 lysine 27 (H3K27) demethylase, has been reported to be implicated in a variety of developmental processes including cell differentiation and cell fate determination and multiple organogenesis. Here, we regulated the transcript level of kdm6bb to study the potential role in controlling the hearing organ development of zebrafish. METHODS: A morpholino antisense oligonucleotide (MO) strategy was used to induce Kdm6b deficiency; immunohistochemical staining and in situ hybridization analysis were conducted to figure out the morphologic alterations and embryonic mechanisms. RESULTS: Kdm6bb is expressed in the primordium and neuromasts at the early stage of zebrafish embryogenesis, suggesting a potential function of Kdm6b in the development of mechanosensory organs. Knockdown of kdm6bb severely influences the cell migration and proliferation in posterior lateral line primordium, abates the number of neuromasts along the trunk, and mRNA-mediated rescue test can partially renew the neuromasts. Loss of kdm6bb might be related to aberrant expressions of chemokine genes encompassing cxcl12a and cxcr4b/cxcr7b in the migrating primordium. Moreover, inhibition of kdm6bb reduces the expression of genes in Fgf signaling pathway, while it increases the axin2 and lef1 expression level of Wnt/β-catenin signaling during the migrating stage. CONCLUSIONS: Collectively, our results revealed that Kdm6b plays an essential role in guiding the migration of primordium and in regulating the deposition of zebrafish neuromasts by mediating the gene expression of chemokines and Wnt and Fgf signaling pathway. Since histone methylation and demethylation are reversible, targeting Kdm6b may present as a novel therapeutic regimen for hearing disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-021-09669-y. Springer Netherlands 2021-10-29 2023 /pmc/articles/PMC10406677/ /pubmed/34716527 http://dx.doi.org/10.1007/s10565-021-09669-y Text en © The Author(s) 2021 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/) . |
spellingShingle | Original Article Tang, Dongmei Lu, Yitong Zuo, Na Yan, Renchun Wu, Cheng Wu, Lijuan Liu, Shaofeng He, Yingzi The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title | The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title_full | The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title_fullStr | The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title_full_unstemmed | The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title_short | The H3K27 demethylase controls the lateral line embryogenesis of zebrafish |
title_sort | h3k27 demethylase controls the lateral line embryogenesis of zebrafish |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406677/ https://www.ncbi.nlm.nih.gov/pubmed/34716527 http://dx.doi.org/10.1007/s10565-021-09669-y |
work_keys_str_mv | AT tangdongmei theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT luyitong theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT zuona theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT yanrenchun theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT wucheng theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT wulijuan theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT liushaofeng theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT heyingzi theh3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT tangdongmei h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT luyitong h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT zuona h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT yanrenchun h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT wucheng h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT wulijuan h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT liushaofeng h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish AT heyingzi h3k27demethylasecontrolsthelaterallineembryogenesisofzebrafish |