Laboratory of Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Oncogene. 2010 Jul 15;29(28):4113-20. doi: 10.1038/onc.2010.150. Epub 2010 May 10.
The Myc-deregulating chromosomal T(12;15)(Igh-Myc) translocation, the hallmark mutation of inflammation- and interleukin 6-dependent mouse plasmacytoma (PCT), is the premier model of cancer-associated chromosomal translocations because it is the only translocation in mice that occurs spontaneously (B lymphocyte lineage) and with predictably high incidence (approximately 85% of PCT), and has a direct counterpart in humans: Burkitt lymphoma t(8;14)(q24;q32) translocation. Here, we report on the development of a genetic system for the detection of T(12;15)(Igh-Myc) translocations in plasma cells of a mouse strain in which an enhanced green fluorescent protein (GFP)-encoding reporter gene has been targeted to Myc. Four of the PCTs that developed in the newly generated translocation reporter mice, designated iGFP(5'Myc), expressed GFP consequent to naturally occurring T(12;15) translocation. GFP expression did not interfere with tumor development or the deregulation of Myc on derivative 12 of translocation, der (12), because the reporter gene was allocated to the reciprocal product of translocation, der (15). Although the described reporter gene approach requires refinement before T(12;15) translocations can be quantitatively detected in vivo, including in B lymphocyte lineage cells that have not yet completed malignant transformation, our findings provide proof of principle that reporter gene tagging of oncogenes in gene-targeted mice can be used to elucidate unresolved questions on the occurrence, distribution and trafficking of cells that have acquired cancer-causing chromosomal translocations of great relevance for humans.
Myc 失调的染色体 T(12;15)(Igh-Myc)易位是炎症和白细胞介素 6 依赖性小鼠浆细胞瘤 (PCT)的标志性突变,是癌症相关染色体易位的主要模型,因为它是唯一在小鼠中自发发生(B 淋巴细胞谱系)且具有可预测高发生率(约 85%的 PCT)的易位,并且在人类中具有直接对应的易位:Burkitt 淋巴瘤 t(8;14)(q24;q32)易位。在这里,我们报告了一种用于检测小鼠品系浆细胞瘤中 T(12;15)(Igh-Myc)易位的遗传系统的开发,该系统将一个增强型绿色荧光蛋白 (GFP)编码报告基因靶向 Myc。在新生成的易位报告小鼠中发展的四个 PCT 中,有四个表达 GFP,这是由于自然发生的 T(12;15)易位所致。GFP 表达并没有干扰肿瘤的发展或易位衍生 12(der(12))上 Myc 的失调,因为报告基因被分配到易位的相互产物 der(15)。虽然描述的报告基因方法需要进一步改进,才能在体内定量检测 T(12;15)易位,包括在尚未完成恶性转化的 B 淋巴细胞谱系细胞中,但我们的发现提供了原则性的证明,即在基因靶向小鼠中对致癌基因进行报告基因标记可以用于阐明关于获得致癌性染色体易位的细胞的发生、分布和运输的未解决问题,这些易位与人类密切相关。