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Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α

Cyclins play a central role in cell-cycle regulation; in mammals, the D family of cyclins consists of cyclin D1, D2, and D3. In Xenopus, only homologs of cyclins D1 and D2 have been reported, while a novel cyclin, cyclin Dx (ccndx), was found to be required for the maintenance of motor neuron progen...

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Autores principales: Lien, Huang-Wei, Yuan, Rey-Yue, Chou, Chih-Ming, Chen, Yi-Chung, Hung, Chin-Chun, Hu, Chin-Hwa, Hwang, Sheng-Ping L., Hwang, Pung-Pung, Shen, Chia-Ning, Chen, Chih-Lung, Cheng, Chia-Hsiung, Huang, Chang-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915019/
https://www.ncbi.nlm.nih.gov/pubmed/27323909
http://dx.doi.org/10.1038/srep28297
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author Lien, Huang-Wei
Yuan, Rey-Yue
Chou, Chih-Ming
Chen, Yi-Chung
Hung, Chin-Chun
Hu, Chin-Hwa
Hwang, Sheng-Ping L.
Hwang, Pung-Pung
Shen, Chia-Ning
Chen, Chih-Lung
Cheng, Chia-Hsiung
Huang, Chang-Jen
author_facet Lien, Huang-Wei
Yuan, Rey-Yue
Chou, Chih-Ming
Chen, Yi-Chung
Hung, Chin-Chun
Hu, Chin-Hwa
Hwang, Sheng-Ping L.
Hwang, Pung-Pung
Shen, Chia-Ning
Chen, Chih-Lung
Cheng, Chia-Hsiung
Huang, Chang-Jen
author_sort Lien, Huang-Wei
collection PubMed
description Cyclins play a central role in cell-cycle regulation; in mammals, the D family of cyclins consists of cyclin D1, D2, and D3. In Xenopus, only homologs of cyclins D1 and D2 have been reported, while a novel cyclin, cyclin Dx (ccndx), was found to be required for the maintenance of motor neuron progenitors during embryogenesis. It remains unknown whether zebrafish possess cyclin D3 or cyclin Dx. In this study, we identified a zebrafish ccndx gene encoding a protein which can form a complex with Cdk4. Through whole-mount in situ hybridization, we observed that zccndx mRNA is expressed in the motor neurons of hindbrain and spinal cord during development. Analysis of a 4-kb promoter sequence of the zccndx gene revealed the presence of HRE sites, which can be regulated by HIF2α. Morpholino knockdown of zebrafish Hif2α and cyclin Dx resulted in the abolishment of isl1 and oligo2 expression in the precursors of motor neurons, and also disrupted axon growth. Overexpression of cyclin Dx mRNA in Hif2α morphants partially rescued zccndx expression. Taken together, our data indicate that zebrafish cyclin Dx plays a role in maintaining the precursors of motor neurons.
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spelling pubmed-49150192016-06-27 Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α Lien, Huang-Wei Yuan, Rey-Yue Chou, Chih-Ming Chen, Yi-Chung Hung, Chin-Chun Hu, Chin-Hwa Hwang, Sheng-Ping L. Hwang, Pung-Pung Shen, Chia-Ning Chen, Chih-Lung Cheng, Chia-Hsiung Huang, Chang-Jen Sci Rep Article Cyclins play a central role in cell-cycle regulation; in mammals, the D family of cyclins consists of cyclin D1, D2, and D3. In Xenopus, only homologs of cyclins D1 and D2 have been reported, while a novel cyclin, cyclin Dx (ccndx), was found to be required for the maintenance of motor neuron progenitors during embryogenesis. It remains unknown whether zebrafish possess cyclin D3 or cyclin Dx. In this study, we identified a zebrafish ccndx gene encoding a protein which can form a complex with Cdk4. Through whole-mount in situ hybridization, we observed that zccndx mRNA is expressed in the motor neurons of hindbrain and spinal cord during development. Analysis of a 4-kb promoter sequence of the zccndx gene revealed the presence of HRE sites, which can be regulated by HIF2α. Morpholino knockdown of zebrafish Hif2α and cyclin Dx resulted in the abolishment of isl1 and oligo2 expression in the precursors of motor neurons, and also disrupted axon growth. Overexpression of cyclin Dx mRNA in Hif2α morphants partially rescued zccndx expression. Taken together, our data indicate that zebrafish cyclin Dx plays a role in maintaining the precursors of motor neurons. Nature Publishing Group 2016-06-21 /pmc/articles/PMC4915019/ /pubmed/27323909 http://dx.doi.org/10.1038/srep28297 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lien, Huang-Wei
Yuan, Rey-Yue
Chou, Chih-Ming
Chen, Yi-Chung
Hung, Chin-Chun
Hu, Chin-Hwa
Hwang, Sheng-Ping L.
Hwang, Pung-Pung
Shen, Chia-Ning
Chen, Chih-Lung
Cheng, Chia-Hsiung
Huang, Chang-Jen
Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title_full Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title_fullStr Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title_full_unstemmed Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title_short Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
title_sort zebrafish cyclin dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915019/
https://www.ncbi.nlm.nih.gov/pubmed/27323909
http://dx.doi.org/10.1038/srep28297
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