Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Tracing early mammalian lineage decisions by single cell genomics.

In plain English

AI plain-English summary

A mouse embryo just six days old will soon be dissected cell by cell to map how a single, blank-slate population transforms into the three distinct layers that build every organ in the body. This matters because gastrulation—the moment when stem cells commit to becoming skin, gut, or muscle—remains poorly understood at the level of individual cells. Existing studies have looked at groups of cells, missing the subtle decisions and random fluctuations that drive each cell’s fate. Without that single-cell resolution, scientists cannot explain how a uniform cluster of cells breaks symmetry and begins to specialise. The consortium will apply cutting-edge techniques to read DNA, RNA, and DNA methylation from nearly every cell in a mouse postimplantation embryo. The result will be a comprehensive map—a Waddington landscape in data form—showing which genes are active, which epigenetic marks are present, and how cells are related to one another. This is fundamental science. There is no immediate practical application. But such maps could eventually guide the directed differentiation of human iPS cells into specific tissues, improving the production of cells for transplantation or drug testing. Past work on developmental biology has similarly laid the groundwork for regenerative medicine.

View original technical description
Lewis Wolpert famously called gastrulation the most important time in your life. During this fascinating process, a pluripotent stem cell population in the early embryo gives rise to the three germ layers from which all organ systems develop. Cell signalling and transcriptional networks are known to regulate aspects of gastrulation, but the precise mechanisms have not been investigated at the single cell level. Thus, new principles remain to be discovered that govern the exit from na ve pluripot ency, epigenetic priming, stochasticity in transcriptional programmes, symmetry breaking, and acquisition of heritable transcriptome patterns. We have brought together a consortium of experts in single cell genomics, mammalian postimplantation development, and computational biology to comprehensively tackle this challenge. We will apply recently established single cell genomics techniques for DNA, RNA, and DNA methylation to profile the majority of the cells in mouse postimplantation embryos. Th is will result in epigenetic and gene expression maps of most cells together with experimentally determined lineage relationships, hence populating a Waddingtonian landscape. Based on such maps, combinations of transcription factors and epigenetic modifiers will be used to experimentally direct differentiation in human iPS cells.

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Researchers

Nichols (EPMC Awardee)Sarah Teichmann (EPMC Awardee)Shankar Srinivas (EPMC Awardee)Wolf Reik (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Epigenetic regulation of cell fate during early mammalian development
Molecular mechanisms of cell fate decisions in gastrulation and early organogenesis
Epigenetic regulation of cell fate decisions at gastrulation
Generating a global view of cell lineage trees during early mouse embryo development
DNA Methylation dynamics during Gastrulation

Original classification

Strategic Award - Science

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