Gladdy Rebecca A, Taylor Michael D, Williams Christine J, Grandal Ildiko, Karaskova Jana, Squire Jeremy A, Rutka James T, Guidos Cynthia J, Danska Jayne S
Program in Developmental Biology, The Hospital for Sick Children and Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
Cancer Cell. 2003 Jan;3(1):37-50. doi: 10.1016/s1535-6108(02)00236-2.
Double-strand DNA breaks (DSB) induce chromosomal translocations and gene amplification in cell culture, but mechanisms by which DSB cause genomic instability in vivo are poorly understood. We show that RAG-1/2-induced DSB cause IgH/c-Myc translocations in leukemic pro-B cells from p53/Prkdc-deficient mice. Strikingly, these translocations were complex, clonally heterogeneous and amplified. We observed reiterated IgH/c-Myc fusions on dicentric chromosomes, suggesting that amplification occurred by repeated cycles of bridge, breakage and fusion. Leukemogenesis was not mitigated in RAG-2/p53/Prkdc-deficient mice, but leukemic pro-B cells lacked IgH/c-Myc translocations. Thus, global genomic instability conferred by p53/Prkdc disruption efficiently transforms pro-B cells lacking RAG-1/2-induced DSB. Unexpectedly, RAG-2/p53/Prkdc-deficient mice also developed leptomeningeal leukemia, providing a novel spontaneous model for this frequent complication of human lymphoblastic malignancies.
双链DNA断裂(DSB)在细胞培养中会诱导染色体易位和基因扩增,但对于DSB在体内导致基因组不稳定的机制,人们了解甚少。我们发现,RAG-1/2诱导的DSB会在p53/Prkdc缺陷小鼠的白血病前B细胞中导致IgH/c-Myc易位。引人注目的是,这些易位是复杂的、克隆异质性的且会发生扩增。我们在双着丝粒染色体上观察到反复出现的IgH/c-Myc融合,这表明扩增是通过桥接、断裂和融合的重复循环发生的。在RAG-2/p53/Prkdc缺陷小鼠中白血病发生并未减轻,但白血病前B细胞缺乏IgH/c-Myc易位。因此,p53/Prkdc破坏导致的整体基因组不稳定有效地转化了缺乏RAG-1/2诱导的DSB的前B细胞。出乎意料的是,RAG-2/p53/Prkkc缺陷小鼠还发生了柔脑膜白血病,为人类淋巴细胞恶性肿瘤这种常见并发症提供了一种新的自发模型。