Suppr超能文献

斑马鱼 cloche 突变体弱等位基因的特征。

Characterization of a weak allele of zebrafish cloche mutant.

机构信息

Key Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases of Guangdong Higher Education Institutes, Department of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.

出版信息

PLoS One. 2011;6(11):e27540. doi: 10.1371/journal.pone.0027540. Epub 2011 Nov 23.

Abstract

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.

摘要

造血是一个复杂而动态的过程,其分子机制仍知之甚少。斑马鱼是研究造血和发育机制的优秀脊椎动物系统。在之前的研究中,我们通过互补测试和初步作图,分离并鉴定了一个新的 cloche(172) (clo(172))突变体,与原始的 cloche (clo) 突变体相比,它是一个新的等位基因。在这里,根据整体原位杂交,我们报告说 clo(172)突变体胚胎中的内皮细胞尽管最初发育,但最终未能形成功能性血管系统。此外,进一步的特征表明,与 clo(s5)突变体相比,clo(172)突变体在原始红细胞和定型造血细胞中表现出较弱的缺陷,而不是完全缺失。相比之下,clo(172)突变体中的原始髓样细胞完全缺失。此外,这些重新出现的定型髓样细胞被证明是从 clo(172)突变体中剩余的造血干细胞 (HSCs) 中产生的,这一点通过 clo(172)runx1(w84x)双突变体中 lyc 的急剧减少得到了证实。总的来说,与 clo(s5)突变体相比,clo(172)突变体是一个较弱的等位基因,因此为研究造血和血管系统的早期发育提供了一个模型,并为进一步了解 cloche 基因的功能提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/712d/3223178/daba4e83e260/pone.0027540.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验