TY - JOUR T1 - DNA Double Strand Breaks cause chromosome loss through sister chromatid tethering in human embryos JF - bioRxiv DO - 10.1101/2022.03.10.483502 SP - 2022.03.10.483502 AU - Jenna Turocy AU - Diego Marin AU - Shuangyi Xu AU - Jia Xu AU - Alex Robles AU - Nathan Treff AU - Dieter Egli Y1 - 2022/01/01 UR - http://biorxiv.org/content/early/2022/03/10/2022.03.10.483502.abstract N2 - Genome editing by DNA double-strand breaks (DSB) is currently being investigated as a tool to treat or even prevent heritable diseases1. However, DNA repair mechanisms in the human embryo remain poorly understood and DSBs may result in chromosome loss 2,3. Here we provide evidence of whole and segmental chromosome loss in over one third of chromosomes 16, 17 and X targeted by CRISPR/Cas9-induced DNA DSB, including pericentromeric and mid-arm sites. Chromosomal changes were asymmetric relative to the Cas9 cut site: segmental losses occurred on both centric as well as acentric chromosome arms, while gains were exclusively found on acentric arms, suggesting that centromeres in broken chromosomes continued to mediate sister chromatid separation. Using this pattern of chromosomal errors, we were able to define new genomic coordinates of the active centromere on chromosome 16. Asymmetry was also found in the attrition of gDNA at the break site: attrition occurred centromeric of the DSB, while telomeric to the break, chromosomal ends were protected. Thus, spindle forces at centromeres and end tethering and protection at DSBs are antagonistic forces that interfere with accurate segregation of sister chromatids. Thereby, a single DSB is sufficient to result in the loss of a chromosome from the embryo. These results highlight the risks of aneuploidy in CRISPR/Cas9 genome editing, while also providing a mechanism for mitotically acquired aneuploidy caused by DNA breaks in human embryos.Competing Interest StatementJ.X., D.M. and N.T. are employees and/or shareholders of Genomic Predictions Inc. D.E. and N.T. have applied for a patent on Cas9 mediated chromosome removal. ER -