Lee Sang-Guk, Park Tae Sung, Won Sung Chul, Song Jaewoo, Lee Kyung-A, Choi Jong Rak, Marschalek Rolf, Meyer Claus
Department of Laboratory Medicine, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, Korea.
Cancer Genet Cytogenet. 2010 Feb;197(1):32-8. doi: 10.1016/j.cancergencyto.2009.10.009.
Translocations involving mixed lineage leukemia (MLL) gene at 11q23 are associated with de novo acute leukemia as well as therapy-related acute leukemia. More than 100 different translocations involving MLL have been described in acute leukemia, with more than 60 translocation partner genes characterized on the molecular level. In addition to various simple translocations affecting MLL, there are also complex forms involving three or more chromosomes. Here, we describe a novel three-way translocation of t(2;19;11)(p12;p13.3;q23) in a patient with acute lymphoblastic leukemia (ALL). In this translocation, the distal 19p13.3 joins the proximal 11q23 on der(11), whereas the distal 11q23 is translocated to 2p12. Three-way translocations involving 11q23 are often difficult to detect with cytogenetic means alone. In the present case, however, the chromosomes involved in the three-way translocation were readily identifiable by GTG banding. The MLL-MLLT1 fusion products from the derivative chromosome 11 were detected by reverse transcriptase-polymerase chain reaction (RT-PCR), and two splicing variant forms were confirmed by cloning and sequencing. Furthermore, the novel third partner gene, NRXN1, was detected by systematic breakpoint analysis using long-distance inverse-PCR methods (LDI-PCR). The apparent three-way translocation thus identified is noteworthy because few studies have reported complex rearrangements involving 11q23 and 19p13.3 in acute leukemias.
涉及11q23处混合谱系白血病(MLL)基因的易位与原发性急性白血病以及治疗相关急性白血病有关。急性白血病中已描述了100多种涉及MLL的不同易位,其中60多种易位伙伴基因已在分子水平上得到鉴定。除了影响MLL的各种简单易位外,还有涉及三条或更多条染色体的复杂形式。在此,我们描述了一名急性淋巴细胞白血病(ALL)患者中一种新的t(2;19;11)(p12;p13.3;q23)三向易位。在这种易位中,19p13.3远端与der(11)上的11q23近端相连,而11q23远端易位至2p12。仅靠细胞遗传学手段通常很难检测到涉及11q23的三向易位。然而,在本病例中,通过GTG显带很容易识别出参与三向易位的染色体。通过逆转录聚合酶链反应(RT-PCR)检测到来自衍生染色体11的MLL-MLLT1融合产物,并通过克隆和测序确认了两种剪接变体形式。此外,使用长距离反向PCR方法(LDI-PCR)通过系统断点分析检测到了新的第三个伙伴基因NRXN1。如此鉴定出的明显三向易位值得注意,因为很少有研究报道急性白血病中涉及11q23和19p13.3的复杂重排。