Ito T, Seyama T, Mizuno T, Hayashi T, Iwamoto K S, Dohi K, Nakamura N, Akiyama M
Department of Radiobiology, Radiation Effects Research Foundation, Hiroshima.
Jpn J Cancer Res. 1993 Feb;84(2):105-9. doi: 10.1111/j.1349-7006.1993.tb02840.x.
The Philadelphia chromosome consists of a reciprocal translocation between the ABL oncogene at chromosome 9q34 and the BCR gene at chromosome 22q11, resulting in the expression of chimeric BCR-ABL mRNAs specific to chronic myelogenous leukemia (CML). Presence of the fusion gene can be detected with high specificity and sensitivity by means of reverse transcription and polymerase chain reaction. Using this assay, it was possible to detect BCR-ABL fusion genes induced among HL60 cells after 100 Gy of X-irradiation in vitro. In total, five fusion gene transcripts were obtained among 10(8) cells examined. These fusion genes contained not only CML-specific BCR-ABL rearrangements, but also other forms of BCR-ABL fusions. These latter genes had junctions of BCR exon 4/ABL exon 2 intervened by a segment of DNA of unknown origin, BCR exon 5/ABL exon 2, and BCR exon 4/ABL exon 2. The results appear to be direct evidence for the induction of the BCR-ABL fusion gene by X-irradiation. In terms of leukemogenesis, it appears that only those cells bearing certain CML-related BCR-ABL fusion genes are positively selected by virtue of a growth advantage in vivo.
费城染色体由9号染色体长臂3区4带的ABL癌基因与22号染色体长臂1区1带的BCR基因相互易位组成,导致慢性髓性白血病(CML)特有的嵌合BCR-ABL mRNA的表达。通过逆转录和聚合酶链反应可以高特异性和高灵敏度地检测融合基因的存在。利用该检测方法,能够在体外100 Gy X射线照射后的HL60细胞中检测到诱导产生的BCR-ABL融合基因。在所检测的10⁸个细胞中,总共获得了5种融合基因转录本。这些融合基因不仅包含CML特异性的BCR-ABL重排,还包括其他形式的BCR-ABL融合。后一种基因具有BCR外显子4/ABL外显子2的连接,中间插入一段未知来源的DNA片段、BCR外显子5/ABL外显子2以及BCR外显子4/ABL外显子2。这些结果似乎是X射线照射诱导BCR-ABL融合基因的直接证据。就白血病发生而言,似乎只有那些携带某些与CML相关的BCR-ABL融合基因的细胞凭借体内的生长优势被正向选择。