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使用多层蛋白质组学技术解析小鼠原肠胚时期的谱系特化过程。

Deciphering lineage specification during early embryogenesis in mouse gastruloids using multilayered proteomics.

机构信息

Department of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, 6525 GA Nijmegen, the Netherlands.

Department of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, 6525 GA Nijmegen, the Netherlands.

出版信息

Cell Stem Cell. 2024 Jul 5;31(7):1072-1090.e8. doi: 10.1016/j.stem.2024.04.017. Epub 2024 May 15.

Abstract

Gastrulation is a critical stage in embryonic development during which the germ layers are established. Advances in sequencing technologies led to the identification of gene regulatory programs that control the emergence of the germ layers and their derivatives. However, proteome-based studies of early mammalian development are scarce. To overcome this, we utilized gastruloids and a multilayered mass spectrometry-based proteomics approach to investigate the global dynamics of (phospho) protein expression during gastruloid differentiation. Our findings revealed many proteins with temporal expression and unique expression profiles for each germ layer, which we also validated using single-cell proteomics technology. Additionally, we profiled enhancer interaction landscapes using P300 proximity labeling, which revealed numerous gastruloid-specific transcription factors and chromatin remodelers. Subsequent degron-based perturbations combined with single-cell RNA sequencing (scRNA-seq) identified a critical role for ZEB2 in mouse and human somitogenesis. Overall, this study provides a rich resource for developmental and synthetic biology communities endeavoring to understand mammalian embryogenesis.

摘要

原肠胚形成是胚胎发育的关键阶段,在此期间胚胎层得以建立。测序技术的进步使得人们能够识别出控制胚胎层及其衍生物出现的基因调控程序。然而,基于蛋白质组学的早期哺乳动物发育研究却很少。为了克服这一问题,我们利用原肠胚和一种多层次的基于质谱的蛋白质组学方法,研究了原肠胚分化过程中(磷酸化)蛋白质表达的全局动态。我们的研究结果揭示了许多具有时间表达和每个胚胎层独特表达谱的蛋白质,我们还使用单细胞蛋白质组学技术对其进行了验证。此外,我们还使用 P300 邻近标记技术对增强子相互作用景观进行了分析,揭示了许多原肠胚特异性转录因子和染色质重塑因子。随后,基于去稳定元件的扰动结合单细胞 RNA 测序(scRNA-seq)鉴定出 ZEB2 在小鼠和人类体节发生中的关键作用。总的来说,这项研究为致力于理解哺乳动物胚胎发生的发育和合成生物学社区提供了丰富的资源。

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