Multi-omics analyses and machine learning prediction of oviductal responses in the presence of gametes and embryos.

IF 6.4 1区 生物学 Q1 BIOLOGY eLife Pub Date : 2025-02-26 DOI:10.7554/eLife.100705
Ryan M Finnerty, Daniel J Carulli, Akshata Hedge, Yanli Wang, Frimpong Boadu, Sarayut Winuthayanon, Jianlin Jack Cheng, Wipawee Winuthayanon
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Abstract

The oviduct is the site of fertilization and preimplantation embryo development in mammals. Evidence suggests that gametes alter oviductal gene expression. To delineate the adaptive interactions between the oviduct and gamete/embryo, we performed a multi-omics characterization of oviductal tissues utilizing bulk RNA-sequencing (RNA-seq), single-cell RNA-sequencing (scRNA-seq), and proteomics collected from distal and proximal at various stages after mating in mice. We observed robust region-specific transcriptional signatures. Specifically, the presence of sperm induces genes involved in pro-inflammatory responses in the proximal region at 0.5 days post-coitus (dpc). Genes involved in inflammatory responses were produced specifically by secretory epithelial cells in the oviduct. At 1.5 and 2.5 dpc, genes involved in pyruvate and glycolysis were enriched in the proximal region, potentially providing metabolic support for developing embryos. Abundant proteins in the oviductal fluid were differentially observed between naturally fertilized and superovulated samples. RNA-seq data were used to identify transcription factors predicted to influence protein abundance in the proteomic data via a novel machine learning model based on transformers of integrating transcriptomics and proteomics data. The transformers identified influential transcription factors and correlated predictive protein expressions in alignment with the in vivo-derived data. Lastly, we found some differences between inflammatory responses in sperm-exposed mouse oviducts compared to hydrosalpinx Fallopian tubes from patients. In conclusion, our multi-omics characterization and subsequent in vivo confirmation of proteins/RNAs indicate that the oviduct is adaptive and responsive to the presence of sperm and embryos in a spatiotemporal manner.

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配子和胚胎存在时输卵管反应的多组学分析和机器学习预测。
输卵管是哺乳动物受精和着床前胚胎发育的场所。有证据表明配子改变了输卵管基因的表达。为了描述输卵管与配子/胚胎之间的适应性相互作用,我们利用大量rna测序(RNA-seq)、单细胞rna测序(scRNA-seq)以及在小鼠交配后不同阶段从远端和近端收集的蛋白质组学对输卵管组织进行了多组学表征。我们观察到强大的区域特异性转录特征。具体来说,精子的存在诱导了性交后0.5天近端区域参与促炎反应的基因。参与炎症反应的基因是由输卵管分泌性上皮细胞特异性产生的。在1.5和2.5 dpc时,参与丙酮酸和糖酵解的基因在近端区域富集,可能为发育中的胚胎提供代谢支持。输卵管液中丰富的蛋白质在自然受精和超排卵样本中观察到差异。RNA-seq数据通过一种基于整合转录组学和蛋白质组学数据转换器的新型机器学习模型,用于识别预计会影响蛋白质组学数据中蛋白质丰度的转录因子。转换器确定了有影响的转录因子和相关的预测蛋白表达,与体内来源的数据一致。最后,我们发现与患者输卵管积水相比,暴露于精子的小鼠输卵管的炎症反应存在一些差异。总之,我们的多组学表征和随后的体内蛋白质/ rna确认表明,输卵管以时空方式适应并响应精子和胚胎的存在。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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