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Experimental Validation of Ankrd17 and Anapc10 Two Novel Meiotic Genes Predicted by Computational Models in Mice

机译:计算模型预测的小鼠新减数分裂基因Ankrd17和Anapc10的实验验证

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摘要

Prophase is a critical stage of meiosis, during which recombination—the landmark event of meiosis—exchanges information between homologous chromosomes. The intractability of mammalian gonads has limited our knowledge on genes or interactions between genes during this key stage. Microarray profiling of gonads in both sexes has generated genome-scale information. However, the asynchronous development of germ cells and the mixed germ/somatic cell population complicate the use of this resource. To elucidate functional networks of meiotic prophase, we have integrated global gene expression with other genome-scale datasets either within or across species. Our computational approaches provide a comprehensive understanding of interactions between genes and can prioritize candidates for targeted experiments. Here, we examined two novel prophase genes predicted by computational models: Ankrd17 and Anapc10. Their expression and localization were characterized in the developing mouse testis using in situ hybridization and immunofluorescence. We found ANKRD17 expression was predominantly restricted to pachytene spermatocytes and round spermatids. ANKRD17 was diffusely distributed throughout the nucleus of pachytene cells but excluded from the XY body and other heterochromatic regions. ANAPC10 was mainly expressed in the cytoplasm of spermatogonia and leptotene and pachytene spermatocytes. These experiments support our computational predictions of Ankrd17 and Anapc10 as potential prophase genes. More importantly, they serve as a proof of concept of our integrative computational and experimental approach, which has delivered a larger candidate gene set to the broader reproductive community.
机译:前期是减数分裂的关键阶段,在此期间重组(减数分裂的标志性事件)在同源染色体之间交换信息。在这个关键阶段,哺乳动物性腺的难治性限制了我们对基因或基因之间相互作用的认识。男女两性腺的微阵列分析已经产生了基因组规模的信息。但是,生殖细胞和生殖/体细胞混合种群的异步发展使这种资源的使用变得复杂。为了阐明减数分裂前期的功能网络,我们将整体基因表达与物种内或物种间的其他基因组规模的数据集进行了整合。我们的计算方法提供了对基因之间相互作用的全面理解,并可以确定目标实验的优先级。在这里,我们检查了由计算模型预测的两个新的前期基因:Ankrd17和Anapc10。使用原位杂交和免疫荧光在发育中的小鼠睾丸中表征它们的表达和定位。我们发现ANKRD17表达主要限于粗线精原细胞和圆形精子。 ANKRD17散布在整个厚膜细胞核中,但不包括在XY体和其他异色区域中。 ANAPC10主要表达于精原细胞的细胞质中,并具有瘦素和瘦素的精细胞。这些实验支持我们对作为潜在前期基因的Ankrd17和Anapc10的计算预测。更重要的是,它们充当了我们的综合计算和实验方法的概念证明,该方法为更广泛的生殖界提供了更大的候选基因集。

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