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Divergent RNA-Binding Proteins DAZL and VASA Induce Meiotic Progression in Human Germ Cells Derived In Vitro

机译:发散的RNA结合蛋白Dazl和Vasa诱导体外衍生的人类生殖细胞中的减数分裂进展

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摘要

Our understanding of human germ cell development is limited in large part due to inaccessibility of early human development to molecular genetic analysis. Pluripotent human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) have been shown to differentiate to cells of all three embryonic germ layers, as well as germ cells in vitro, and thus may provide a model for the study of the genetics and epigenetics of human germline. Here, we examined whether intrinsic germ cell translational, rather than transcriptional, factors might drive germline formation and/or differentiation from human pluripotent stem cells in vitro. We observed that, with overexpression of VASA (DDX4) and/or DAZL (Deleted in Azoospermia Like), both hESCs and iPSCs differentiated to primordial germ cells, and maturation and progression through meiosis was enhanced. These results demonstrate that evolutionarily unrelated and divergent RNA-binding proteins can promote meiotic progression of human-derived germ cells in vitro. These studies describe an in vitro model for exploring specifics of human meiosis, a process that is remarkably susceptible to errors that lead to different infertility-related diseases.
机译:由于早期人类发展对分子遗传分析,我们对人类生殖细胞发展的理解是有限的。已显示多能人胚胎干细胞(HESC)和诱导多能干细胞(IPSC)分化为所有三种胚胎胚层的细胞,以及体外生殖细胞,因此可以为遗传学研究提供模型和人类种系的表观遗传学。在这里,我们检查了内在胚芽细胞翻译,而不是转录的因素是否可能在体外推动种子形成和/或分化。我们观察到,随着VASA(DDX4)和/或DAZL(如Zzoospermia缺失)的过表达,HESC和IPSC都与原始生殖细胞分化,并通过减数分裂进行了成熟和进展。这些结果表明,进化不相关和发散的RNA结合蛋白可以在体外促进人源生殖细胞的减数分裂进展。这些研究描述了一种用于探索人数分裂的细节的体外模型,这一过程非常容易受到导致不同不孕症相关疾病的错误。

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