European Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
Genetics. 2024 Nov 6;228(3). doi: 10.1093/genetics/iyae150.
Multiple pathways are known to suppress the formation of gross chromosomal rearrangements (GCRs), which can cause human diseases including cancer. In contrast, much less is known about pathways that promote their formation. The spindle assembly checkpoint (SAC), which ensures the proper separation of chromosomes during mitosis, has been reported to promote GCR, possibly by delaying mitosis to allow GCR-inducing DNA repair to occur. Here, we show that this conclusion is the result of an experimental artifact arising from the synthetic lethality caused by the disruption of the SAC and loss of the CIN8 gene, which is often lost in the genetic assay used to select for GCRs. After correcting for this artifact, we find no role of the SAC in promoting GCR.
已知多种途径可抑制染色体结构重排(GCR)的形成,GCR 可导致包括癌症在内的人类疾病。相比之下,人们对促进 GCR 形成的途径知之甚少。纺锤体组装检查点(SAC)可确保有丝分裂过程中染色体的正确分离,据报道,SAC 可促进 GCR 的形成,可能是通过延迟有丝分裂以使 GCR 诱导的 DNA 修复发生。在这里,我们表明,这一结论是由 SAC 破坏和 CIN8 基因缺失引起的合成致死性所导致的实验假象的结果,CIN8 基因在用于选择 GCR 的遗传检测中经常丢失。在纠正了这种假象之后,我们发现 SAC 在促进 GCR 方面没有作用。