New insights into early human embryo development

Fresh insights into early human embryo development
Fredrik Lanner, Sophie Petropoulos, Rickard Sandberg and colleagues at Karolinska Institutet, Sweden, have analyzed the embryo's first week of development in detail. Credit: Ulf Sirborn

Researchers at Karolinska Institutet and the Ludwig Cancer Research in Stockholm, Sweden have conducted a detailed molecular analysis of the embryo's first week of development. Their results show that there are considerable differences in embryonic development between humans and mice, which is the most common organism of study in this field. The new study, which is published in the journal Cell, also shows that genes on the X chromosome are regulated differently.

Early human embryonic development is difficult to study, and most of our knowledge comes from mice. During the first seven days of fertilisation, the egg develops from a single cell to a blastocyst, a hollow cluster of some 200 to 300 cells. It is during this time that the first three appear: the trophectoderm, which gives rise to the placenta, the hypoblast, which forms the embryonic endoderm, and the that go to make up the embryo itself. If the embryo is to adhere to the uterus wall and pregnancy commence, all these three cell types must mature properly. However, exactly when and in which order and how the cell types form in humans has not been known.

By detecting gene expression in individual cells, from donated human embryos that were not used for IVF treatment, two research groups led by Rickard Sandberg and Fredrik Lanner have managed to identify which genes are used in the embryo's cells at different times during the first week of development. They found that the first three cell types form later and seem to mature more simultaneously in the human than in the mouse.

"The fundamental knowledge generated by our research doesn't only help us understand better, it also tells us more about how pluripotent cells are formed and regulated in its early stages," says Fredrik Lanner at Karolinska Institutet's Department of Clinical Science, Intervention and Technology. "This is important for the use of in regenerative medicine."

The researchers also found that the expression of genes situated on the X chromosome is subject to an unexpected expression pattern. The X chromosome has a particular gene regulation problem, since women's cells have two X chromosomes, while men only have a copy (XY). To avoid women having twice the level of expression of all genes on the X chromosome as men, women's must offset the gene expression. In mice, where this process is well-studied, one of the two X chromosomes is simply shut off during the first week. However, it has always been uncertain if this process even begins during the first week of .

"What we've been able to demonstrate is that dose balance is gradually attained during day 4 to 7, interestingly through a completely new manner in which the from both X chromosomes in the female embryo is suppressed," says Rickard Sandberg of Karolinska Institutet's Department of Cell and Molecular Biology and the Ludwig Cancer Research.

More information: 'Single-cell RNA-seq reveals lineage and X chromosome dynamics in human preimplantation embryos', Sophie Petropoulos, Daniel Edsga?rd, Bjo?rn Reinius, Qiaolin Deng, Sarita Pauliina Panula, Simone Codeluppi, Alvaro Plaza Reyes, Sten Linnarsson, Rickard Sandberg, and Fredrik Lanner, Cell, published online 7 April 2016, DOI: 10.1016/j.cell.2016.03.023

Journal information: Cell

Citation: New insights into early human embryo development (2016, April 7) retrieved 6 December 2023 from
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