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Characterization of a Weak Allele of Zebrafish cloche Mutant
Hematopoiesis is a complicated and dynamic process about which the molecular mechanisms remain poorly understood. Danio rerio (zebrafish) is an excellent vertebrate system for studying hematopoiesis and developmental mechanisms. In the previous study, we isolated and identified a cloche (172) (clo (...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223178/ https://www.ncbi.nlm.nih.gov/pubmed/22132109 http://dx.doi.org/10.1371/journal.pone.0027540 |
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author | Ma, Ning Huang, Zhibin Chen, Xiaohui He, Fei Wang, Kun Liu, Wei Zhao, Linfeng Xu, Xiangmin Liao, Wangjun Ruan, Hua Luo, Shenqiu Zhang, Wenqing |
author_facet | Ma, Ning Huang, Zhibin Chen, Xiaohui He, Fei Wang, Kun Liu, Wei Zhao, Linfeng Xu, Xiangmin Liao, Wangjun Ruan, Hua Luo, Shenqiu Zhang, Wenqing |
author_sort | Ma, Ning |
collection | PubMed |
description | Hematopoiesis is a complicated and dynamic process about which the molecular mechanisms remain poorly understood. Danio rerio (zebrafish) is an excellent vertebrate system for studying hematopoiesis and developmental mechanisms. In the previous study, we isolated and identified a cloche (172) (clo (172)) mutant, a novel allele compared to the original cloche (clo) mutant, through using complementation test and initial mapping. Here, according to whole mount in-situ hybridization, we report that the endothelial cells in clo (172) mutant embryos, although initially developed, failed to form the functional vascular system eventually. In addition, further characterization indicates that the clo (172) mutant exhibited weaker defects instead of completely lost in primitive erythroid cells and definitive hematopoietic cells compared with the clo (s5) mutant. In contrast, primitive myeloid cells were totally lost in clo (172) mutant. Furthermore, these reappeared definitive myeloid cells were demonstrated to initiate from the remaining hematopoietic stem cells (HSCs) in clo (172) mutant, confirmed by the dramatic decrease of lyc in clo (172) runx1(w84x) double mutant. Collectively, the clo (172) mutant is a weak allele compared to the clo (s5) mutant, therefore providing a model for studying the early development of hematopoietic and vascular system, as well as an opportunity to further understand the function of the cloche gene. |
format | Online Article Text |
id | pubmed-3223178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32231782011-11-30 Characterization of a Weak Allele of Zebrafish cloche Mutant Ma, Ning Huang, Zhibin Chen, Xiaohui He, Fei Wang, Kun Liu, Wei Zhao, Linfeng Xu, Xiangmin Liao, Wangjun Ruan, Hua Luo, Shenqiu Zhang, Wenqing PLoS One Research Article Hematopoiesis is a complicated and dynamic process about which the molecular mechanisms remain poorly understood. Danio rerio (zebrafish) is an excellent vertebrate system for studying hematopoiesis and developmental mechanisms. In the previous study, we isolated and identified a cloche (172) (clo (172)) mutant, a novel allele compared to the original cloche (clo) mutant, through using complementation test and initial mapping. Here, according to whole mount in-situ hybridization, we report that the endothelial cells in clo (172) mutant embryos, although initially developed, failed to form the functional vascular system eventually. In addition, further characterization indicates that the clo (172) mutant exhibited weaker defects instead of completely lost in primitive erythroid cells and definitive hematopoietic cells compared with the clo (s5) mutant. In contrast, primitive myeloid cells were totally lost in clo (172) mutant. Furthermore, these reappeared definitive myeloid cells were demonstrated to initiate from the remaining hematopoietic stem cells (HSCs) in clo (172) mutant, confirmed by the dramatic decrease of lyc in clo (172) runx1(w84x) double mutant. Collectively, the clo (172) mutant is a weak allele compared to the clo (s5) mutant, therefore providing a model for studying the early development of hematopoietic and vascular system, as well as an opportunity to further understand the function of the cloche gene. Public Library of Science 2011-11-23 /pmc/articles/PMC3223178/ /pubmed/22132109 http://dx.doi.org/10.1371/journal.pone.0027540 Text en Ma et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ma, Ning Huang, Zhibin Chen, Xiaohui He, Fei Wang, Kun Liu, Wei Zhao, Linfeng Xu, Xiangmin Liao, Wangjun Ruan, Hua Luo, Shenqiu Zhang, Wenqing Characterization of a Weak Allele of Zebrafish cloche Mutant |
title | Characterization of a Weak Allele of Zebrafish cloche Mutant |
title_full | Characterization of a Weak Allele of Zebrafish cloche Mutant |
title_fullStr | Characterization of a Weak Allele of Zebrafish cloche Mutant |
title_full_unstemmed | Characterization of a Weak Allele of Zebrafish cloche Mutant |
title_short | Characterization of a Weak Allele of Zebrafish cloche Mutant |
title_sort | characterization of a weak allele of zebrafish cloche mutant |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223178/ https://www.ncbi.nlm.nih.gov/pubmed/22132109 http://dx.doi.org/10.1371/journal.pone.0027540 |
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