小鼠原肠胚形成和早期器官发生的时空图谱,探索轴向模式,并将体外模型投射到体内空间。

IF 6.9 1区 生物学 Q1 CELL BIOLOGY
Luke T G Harland, Tim Lohoff, Noushin Koulena, Nico Pierson, Constantin Pape, Farhan Ameen, Jonathan Griffiths, Bart Theeuwes, Nicola K Wilson, Anna Kreshuk, Wolf Reik, Jennifer Nichols, Long Cai, John C Marioni, Berthold Göttgens, Shila Ghazanfar
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引用次数: 0

摘要

在原肠胚形成过程中,小鼠外胚层细胞形成了三个胚层,这些胚层建立了机体计划并启动了器官发生。虽然单细胞图谱提高了我们对谱系多样化的理解,但分化的空间方面仍然定义不清。在这里,我们将空间转录组学应用于胚胎E7.25和E7.5天的小鼠胚胎,并将这些数据与现有的E8.5空间和E6.5-E9.5单细胞RNA-seq图谱进行整合。这产生了一个超过150,000个细胞的时空图谱,其中包含82个精细的细胞类型注释。该资源能够探索基因在前后轴和背腹轴上的表达动态,揭示在原始条纹中指导中胚层命运决定的空间逻辑。我们还开发了一个计算管道,将额外的单细胞数据集投射到这个框架中进行比较分析。通过交互式门户网站免费访问,该图谱为发育和干细胞生物学社区提供了一个有价值的工具,可以在空间和时间背景下研究小鼠胚胎发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A spatiotemporal atlas of mouse gastrulation and early organogenesis to explore axial patterning and project in vitro models onto in vivo space.

During gastrulation, mouse epiblast cells form the three germ layers that establish the body plan and initiate organogenesis. While single-cell atlases have advanced our understanding of lineage diversification, spatial aspects of differentiation remain poorly defined. Here, we applied spatial transcriptomics to mouse embryos at embryonic (E) E7.25 and E7.5 days and integrated these data with existing E8.5 spatial and E6.5-E9.5 single-cell RNA-seq atlases. This resulted in a spatiotemporal atlas of over 150,000 cells with 82 refined cell-type annotations. The resource enables exploration of gene expression dynamics across anterior-posterior and dorsal-ventral axes, uncovering spatial logic guiding mesodermal fate decisions in the primitive streak. We also developed a computational pipeline to project additional single-cell datasets into this framework for comparative analysis. Freely accessible through an interactive web portal, this atlas offers a valuable tool for the developmental and stem cell biology communities to investigate mouse embryogenesis in a spatial and temporal context.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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