Department of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Nat Commun. 2021 Oct 6;12(1):5855. doi: 10.1038/s41467-021-26097-y.
Karyotype alterations have emerged as on-target complications from CRISPR-Cas9 genome editing. However, the events that lead to these karyotypic changes in embryos after Cas9-treatment remain unknown. Here, using imaging and single-cell genome sequencing of 8-cell stage embryos, we track both spontaneous and Cas9-induced karyotype aberrations through the first three divisions of embryonic development. We observe the generation of abnormal structures of the nucleus that arise as a consequence of errors in mitosis, including micronuclei and chromosome bridges, and determine their contribution to common karyotype aberrations including whole chromosome loss that has been recently reported after editing in embryos. Together, these data demonstrate that Cas9-mediated germline genome editing can lead to unwanted on-target side effects, including major chromosome structural alterations that can be propagated over several divisions of embryonic development.
染色体组型改变已成为 CRISPR-Cas9 基因组编辑的靶向并发症。然而,Cas9 处理后胚胎中导致这些染色体组型变化的事件尚不清楚。在这里,我们使用 8 细胞期胚胎的成像和单细胞基因组测序,通过胚胎发育的前三个分裂跟踪自发和 Cas9 诱导的染色体组型异常。我们观察到核的异常结构的产生,这是有丝分裂错误的结果,包括微核和染色体桥,并确定它们对常见染色体异常的贡献,包括最近在胚胎编辑后报道的整条染色体缺失。总之,这些数据表明 Cas9 介导的种系基因组编辑可能导致不必要的靶向副作用,包括可能在胚胎发育的多个分裂中传播的主要染色体结构改变。