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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 (...

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Detalles Bibliográficos
Autores principales: Ma, Ning, Huang, Zhibin, Chen, Xiaohui, He, Fei, Wang, Kun, Liu, Wei, Zhao, Linfeng, Xu, Xiangmin, Liao, Wangjun, Ruan, Hua, Luo, Shenqiu, Zhang, Wenqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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
Descripción
Sumario: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.