Early developmental asymmetries in cell lineage trees in living individuals

Author:

Fasching Liana1ORCID,Jang Yeongjun2ORCID,Tomasi Simone1,Schreiner Jeremy1ORCID,Tomasini Livia1ORCID,Brady Melanie V.1ORCID,Bae Taejeong2ORCID,Sarangi Vivekananda2,Vasmatzis Nikolaos2ORCID,Wang Yifan2ORCID,Szekely Anna3ORCID,Fernandez Thomas V.14ORCID,Leckman James F.14,Abyzov Alexej2ORCID,Vaccarino Flora M.156ORCID

Affiliation:

1. Child Study Center, Yale University, New Haven, CT 06520, USA.

2. Department of Quantitative Health Sciences, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.

3. Department of Neurology, Yale University, New Haven, CT 06520, USA.

4. Department of Psychiatry, Yale University, New Haven, CT 06520, USA.

5. Department of Neuroscience, Yale University, New Haven, CT 06520, USA.

6. Yale Kavli Institute for Neuroscience, New Haven, CT 06520, USA.

Abstract

Genomic sleuthing spots early divergence After fertilization, the human zygote divides into two cells. Fasching et al. used genomic analysis from cellular samples taken much later in development to back-calculate the cell division trees that went before. Although the first cell division in human development looks symmetrical from the outside, the fates followed by daughter cells from each of those first two blastomeres are anything but the same. As much as 90% of blood cells are derived from just one of the first two blastomeres. Science , this issue p. 1245

Funder

National Institute of Mental Health

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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