Trachana Varvara, van Wely Karel H M, Guerrero Astrid Alonso, Fütterer Agnes, Martínez-A Carlos
Department of Immunology and Oncology, Centro Nacional de Biotecnología/Consejo Superior de Investigaciones Cientificas, Darwin 3, Campus de Cantoblanco, E-28049 Madrid, Spain.
Proc Natl Acad Sci U S A. 2007 Feb 20;104(8):2691-6. doi: 10.1073/pnas.0611132104. Epub 2007 Feb 13.
Numerical and/or structural centrosome abnormalities have been correlated with most solid tumors and hematological malignancies. Tumorigenesis also is linked to defects in the mitotic or spindle assembly checkpoint, a key control mechanism that ensures accurate segregation of chromosomes during mitosis. We have reported that targeted disruption of the Dido gene causes a transplantable myelodysplastic/myeloproliferative disease in mice. Here, we report that Dido3, the largest splice variant of the Dido gene, is a centrosome-associated protein whose disruption leads to supernumerary centrosomes, failure to maintain cellular mitotic arrest, and early degradation of the mitotic checkpoint protein BubR1. These aberrations result in enhanced aneuploidy in the Dido mutant cells. Dido gene malfunction thus is reported to be part of an impaired signaling cascade that results in a defective mitotic checkpoint, leading to chromosome instability.
数值和/或结构中心体异常与大多数实体瘤和血液系统恶性肿瘤相关。肿瘤发生也与有丝分裂或纺锤体组装检查点的缺陷有关,这是一种关键的控制机制,可确保有丝分裂期间染色体的准确分离。我们曾报道,靶向破坏Dido基因会在小鼠中引发一种可移植的骨髓增生异常/骨髓增殖性疾病。在此,我们报告Dido基因最大的剪接变体Dido3是一种与中心体相关的蛋白质,其破坏会导致中心体数量过多、无法维持细胞有丝分裂停滞以及有丝分裂检查点蛋白BubR1的早期降解。这些异常导致Dido突变细胞中的非整倍体增加。因此,据报道Dido基因功能异常是信号级联受损的一部分,导致有丝分裂检查点缺陷,进而导致染色体不稳定。