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The developmental origins of sex-biased expression in cardiac development

机译:心脏发育中性别偏向表达的发展起源

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摘要

BackgroundExpression patterns between males and females vary in every adult tissue, even in organs with no conspicuous dimorphisms such as the heart. While studies of male and female differences have traditionally focused on the influence of sex hormones, these do not account for all the differences at the molecular and epigenetic levels. We previously reported that a substantial number of genes were differentially expressed in male and female mouse embryonic stem (ES) cells and revealed dose-dependent enhancer activity in response to Prdm14, a key pluripotency factor expressed more highly in female ES cells. In this work, we investigated the role of Prdm14 in establishing sex-specific gene expression networks. We surveyed the sex-specific landscape in early embryogenesis with special reference to cardiac development. We generated sex-specific co-expression networks from mouse ES cells, examined the presence of sex-specific chromatin domains, and analyzed previously published datasets from different developmental time points to characterize how sex-biased gene expression waxes and wanes to evaluate whether sex-biased networks are detectable throughout heart development.
机译:背景技术在每个成年组织中,即使在没有明显二态性的器官(如心脏)中,男性和女性之间的表达方式也各不相同。传统上,关于男性和女性差异的研究都集中在性激素的影响上,但这些并不能解释分子和表观遗传水平上的所有差异。我们以前报道过,大量基因在雄性和雌性小鼠胚胎干(ES)细胞中差异表达,并揭示了对Prdm14的剂量依赖性增强子活性,Prdm14是在雌性ES细胞中表达更高的关键多能性因子。在这项工作中,我们调查了Prdm14在建立性别特异性基因表达网络中的作用。我们调查了早期胚胎发生过程中的性别特异性景观,并特别提到了心脏发育。我们从小鼠ES细胞生成了性别特异性共表达网络,检查了性别特异性染色质结构域的存在,并分析了来自不同发育时间点的先前发表的数据集,以表征性别偏向的基因表达如何起伏和减弱,从而评估性别是否在整个心脏发育过程中都可以检测到有偏见的网络。

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