Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid 28049, Spain.
Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid 28029, Spain.
Biol Open. 2022 Aug 15;11(8). doi: 10.1242/bio.059401. Epub 2022 Jul 29.
Most studies addressing chromatin behaviour during preimplantation development are based on biochemical assays that lack spatial and cell-specific information, crucial during early development. Here, we describe the changes in chromatin taking place at the transition from totipotency to lineage specification, by using direct stochastical optical reconstruction microscopy (dSTORM) in whole-mount embryos during the first stages of mouse development. Through the study of two post-translational modifications of Histone 3 related to active and repressed chromatin, H3K4me3 and H3K9me3 respectively, we obtained a time-course of chromatin states, showing spatial differences between cell types, related to their differentiation state. This analysis adds a new layer of information to previous biochemical studies and provides novel insight to current models of chromatin organisation during the first stages of development.
大多数研究胚胎植入前发育过程中的染色质行为的研究都是基于缺乏空间和细胞特异性信息的生化分析,而这些信息在早期发育过程中至关重要。在这里,我们通过在小鼠发育的早期阶段使用直接随机光学重建显微镜(dSTORM)对整个胚胎进行研究,描述了从全能性到谱系特化的过渡过程中染色质的变化。通过研究与活性和抑制性染色质相关的两种组蛋白 3 的翻译后修饰,即 H3K4me3 和 H3K9me3,我们获得了染色质状态的时程,显示了与细胞分化状态相关的细胞类型之间的空间差异。这项分析为以前的生化研究增加了一个新的信息层,并为当前关于早期发育过程中染色质组织的模型提供了新的见解。