Master gene NANOG controls start of human embryo development

Researchers have identified the gene NANOG as the key switch that initiates the developmental program resulting in cells forming a human body. The finding came from precise DNA edits to fertilized human eggs using CRISPR base editing.

Kathy Niakan at the University of Cambridge led the work, which revealed that NANOG plays a different role in people than in mice. When the gene was disabled in donated human eggs, none of the cells developed into those that form the embryo itself.

The embryos still looked normal under a microscope. Niakan noted that this could explain why many IVF embryos fail to implant even when they appear viable.

The study, published in Nature, also showed that base editing reduces some risks compared with earlier CRISPR methods. Niakan stressed that the technology remains far from use in creating gene-edited children.

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Researchers in New York have tested an improved gene-editing method on healthy human embryos donated for research. The study shows mixed success in making precise DNA changes while avoiding some unintended mutations.

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Bootstrap Bio and Manhattan Genomics, biotech firms launched last year to pursue human embryo editing for preventing serious diseases, have closed their doors. The companies cited financial difficulties and internal conflicts as reasons for the shutdowns. The developments highlight challenges in the controversial field of gene-edited babies.

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