Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development
Both Pax1 and Pax9 belong to the important paired box gene family (PAX), which mainly participates in animal development and sclerotome differentiation. To date, the precise molecular mechanism and related signaling pathway of Pax1 remain unclear. In our study, microinjection of morpholino- (MO-) mo...
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pubmed-41473602014-09-07 Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development Chen, Xuemei Huang, Huizhe Wang, Hua Guo, Fengjin Du, Xiaogang Ma, Linqiang Zhao, Liang Pan, Zhuma Gui, Haibo Yuan, Taixian Liu, Xin Song, Lin Wang, Yiquan He, Junling Lei, Han Gao, Rui Research Article Both Pax1 and Pax9 belong to the important paired box gene family (PAX), which mainly participates in animal development and sclerotome differentiation. To date, the precise molecular mechanism and related signaling pathway of Pax1 remain unclear. In our study, microinjection of morpholino- (MO-) modified antisense oligonucleotides against pax1b induced pectoral fin bud defects. Furthermore, we demonstrate that the phenotypes caused by the knockdown of Pax1b in zebrafish could not be phenocopied by pax9 MO and could not be rescued by either Pax1a or Pax9 overexpression. We further find that Pax1b affects the expression of col2a1, Uncx4.1, Noggin3, and aggrecan, confirming the role of Pax1b in chondrocyte differentiation and bone maturation. Moreover, we identify an interaction between PAX1 and FOXO1 and find that the interaction was enhanced under hypoxia stress. Together, this evidence for cell death caused by pax1b knockdown provides new insight into the role of the Pax protein family in cell fate determination and tissue specification. Hindawi Publishing Corporation 2014 2014-08-13 /pmc/articles/PMC4147360/ /pubmed/25197636 http://dx.doi.org/10.1155/2014/309385 Text en Copyright © 2014 Xuemei Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Chen, Xuemei Huang, Huizhe Wang, Hua Guo, Fengjin Du, Xiaogang Ma, Linqiang Zhao, Liang Pan, Zhuma Gui, Haibo Yuan, Taixian Liu, Xin Song, Lin Wang, Yiquan He, Junling Lei, Han Gao, Rui |
spellingShingle |
Chen, Xuemei Huang, Huizhe Wang, Hua Guo, Fengjin Du, Xiaogang Ma, Linqiang Zhao, Liang Pan, Zhuma Gui, Haibo Yuan, Taixian Liu, Xin Song, Lin Wang, Yiquan He, Junling Lei, Han Gao, Rui Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
author_facet |
Chen, Xuemei Huang, Huizhe Wang, Hua Guo, Fengjin Du, Xiaogang Ma, Linqiang Zhao, Liang Pan, Zhuma Gui, Haibo Yuan, Taixian Liu, Xin Song, Lin Wang, Yiquan He, Junling Lei, Han Gao, Rui |
author_sort |
Chen, Xuemei |
title |
Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
title_short |
Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
title_full |
Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
title_fullStr |
Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
title_full_unstemmed |
Characterization of Zebrafish Pax1b and Pax9 in Fin Bud Development |
title_sort |
characterization of zebrafish pax1b and pax9 in fin bud development |
description |
Both Pax1 and Pax9 belong to the important paired box gene family (PAX), which mainly participates in animal development and sclerotome differentiation. To date, the precise molecular mechanism and related signaling pathway of Pax1 remain unclear. In our study, microinjection of morpholino- (MO-) modified antisense oligonucleotides against pax1b induced pectoral fin bud defects. Furthermore, we demonstrate that the phenotypes caused by the knockdown of Pax1b in zebrafish could not be phenocopied by pax9 MO and could not be rescued by either Pax1a or Pax9 overexpression. We further find that Pax1b affects the expression of col2a1, Uncx4.1, Noggin3, and aggrecan, confirming the role of Pax1b in chondrocyte differentiation and bone maturation. Moreover, we identify an interaction between PAX1 and FOXO1 and find that the interaction was enhanced under hypoxia stress. Together, this evidence for cell death caused by pax1b knockdown provides new insight into the role of the Pax protein family in cell fate determination and tissue specification. |
publisher |
Hindawi Publishing Corporation |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147360/ |
_version_ |
1613128588080447488 |