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单细胞分辨率解析胚胎发生的谱系分辨分子图谱。

A lineage-resolved molecular atlas of embryogenesis at single-cell resolution.

机构信息

Department of Genome Sciences, University of Washington, Seattle, WA, USA.

Genomics and Computational Biology Graduate Group, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Science. 2019 Sep 20;365(6459). doi: 10.1126/science.aax1971. Epub 2019 Sep 5.

Abstract

is an animal with few cells but a wide diversity of cell types. In this study, we characterize the molecular basis for their specification by profiling the transcriptomes of 86,024 single embryonic cells. We identify 502 terminal and preterminal cell types, mapping most single-cell transcriptomes to their exact position in ' invariant lineage. Using these annotations, we find that (i) the correlation between a cell's lineage and its transcriptome increases from middle to late gastrulation, then falls substantially as cells in the nervous system and pharynx adopt their terminal fates; (ii) multilineage priming contributes to the differentiation of sister cells at dozens of lineage branches; and (iii) most distinct lineages that produce the same anatomical cell type converge to a homogenous transcriptomic state.

摘要

是一种细胞数量较少但细胞类型多样的动物。在这项研究中,我们通过分析 86024 个单个胚胎细胞的转录组,来描绘它们特化的分子基础。我们确定了 502 个终末和前体细胞类型,将大多数单细胞转录组映射到它们在 '不变谱系中的精确位置。利用这些注释,我们发现:(i) 细胞谱系与其转录组之间的相关性从中胚层晚期到晚期逐渐增加,然后随着神经系统和咽的细胞采用其终末命运而大幅下降;(ii) 多谱系启动有助于数十个谱系分支中姐妹细胞的分化;(iii) 产生相同解剖学细胞类型的大多数不同谱系趋于一致的转录组状态。

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