Magdalena Żernicka-Goetz

Żernicka-Goetz was born in Warsaw, Poland in 1963.[1] She received her Master of Science degree (summa cum laude) in developmental biology (1988) and her PhD degree in the developmental biology of mammals (1993) from the University of Warsaw, with one year (1990–91) spent at the University of Oxford. She carried out her Ph.D. studies with Andrzej Tarkowski (Warsaw) and Chris Graham (Oxford).[9]

After obtaining her Ph.D., Zernicka-Goetz spent two years as a postdoctoral European Molecular Biology Organization (EMBO) fellow with Martin Evans in the Wellcome Trust / Cancer Research UK Institute (now the Gurdon Institute) in Cambridge. In 1997, she started her independent group in the Gurdon Institute where she was a Lister Institute Senior Research Fellow (1997-2002) and subsequently a Wellcome Trust Senior Research Fellow. In 2014, she moved her laboratory to the Department of Physiology, Development and Neuroscience of the University of Cambridge. In 2007, she was awarded a readership and in 2010 a professorship at the University of Cambridge.

Upon setting up her independent group in 1997, she studied the mechanisms regulating early mammalian development. To do this, she was first to establish RNA interference in mammalian cells to determine cell fate in the mouse embryos.[10] At that time, she also began to trace the origins and destinies of cells in the preimplantation mouse embryo that let her to discover that cell fate specification begins earlier than expected,[11][12][13][14] an unexpected discovery but subsequently validated by her group and others. She found that this development of cell identity begins with heterogeneity in epigenetic regulation at the 4-cell stage[15] that directs a molecular cascade establishing cell polarity, position and fate.[16][17][18][19]

Her recent development of systems permitting both mouse and human embryogenesis during implantation and early post-implantation stages in vitro allowed her to reveal that mouse and human embryo remodelling at implantation is done autonomously by the embryo. She uncovered the mechanism underlying embryo remodelling between the blastocyst and gastrula stages that has led to a change in the textbook model.[20][21] Her demonstration of the self-organisation of human embryos developing in vitro until day 13/14, gastrulation, has provided an unprecedented opportunity to study human development at previously inaccessible and critical stages.[22] This discovery was hailed as the people's choice for the scientific breakthrough of 2016 by Science magazine.[23][24] The knowledge she gained through her work on how the embryo develops during the blastocyst to gastrula transition, allowed her to mimic these developmental processes with different types of stem cells in vitro. This led her to the pioneering success of constructing embryo-like structures from pluripotent embryonic and multipotent extra-embryonic (trophoblast) stem cells in a 3D scaffold of extra-cellular matrix proteins in vitro.[25] These "synthetic embryos" recapitulate the natural architecture of the embryo and their patterns of gene expression leading to the specification of the germ layers and germ cells. This system allowed her to identify signalling pathways responsible for morphogenesis of stem cells into embryos. Together these models bring outstanding potential for understanding development and for regenerative medicine. In 2023, her team created the first human embryo models.[26][27]

Żernicka-Goetz's group have shown that sperm entry induces actomyosin-driven cytoplasmic flows that are predictive of successful development to birth in the mouse. This provides an opportunity to identify quantitatively and non-invasively the healthiest embryos to transfer to would-be-mothers in IVF.[28]

Stimulated by the finding of placental cells with abnormal chromosome complements (aneuploid cells) in her own pregnancy, she began to study the consequence of aneuploidy upon development in a mouse model. Her lab generated an experimental model to find that aneuploid cells arising during embryogenesis in the mouse embryo become eliminated by apoptosis in embryonic but not extra-embryonic tissues. This gives insight into why mosaic aneuploidy identified by chorionic-villus-sampling can be tolerated in human pregnancies.[29]

The potential impact of Żernicka-Goetz's work is now becoming widely recognised through her public engagement.[30][31]

Her book “The Dance of Life” co-authored with Roger Highfield,[32] describes her scientific and personal journey devoted to understanding the earliest stages of our own life and the critical issue of women in science.

Żernicka-Goetz married David Glover in 2000 and has two children.[1]