Liang J, Prouty L, Williams B J, Dayton M A, Blanchard K L
Department of Molecular Biology and Biochemistry, Pediatrics, Urology, and Medicine, the Feist-Weiller Cancer Center, Louisiana State University Medical School, Shreveport, LA, USA.
Blood. 1998 Sep 15;92(6):2118-22.
Chromosomal abnormalities in acute leukemia have led to the discovery of many genes involved in normal hematopoiesis and in malignant transformation. We have identified the fusion partners in an inv(8)(p11q13) from a patient with acute mixed lineage leukemia. We show by fluorescence in situ hybridization (FISH) analysis, Southern blotting, and reverse transcriptase-polymerase chain reaction (RT-PCR) that the genes for MOZ, monocytic leukemia zinc finger protein, and TIF2, transcriptional intermediary factor 2, are involved in the inv(8)(p11q13). We demonstrate that the inversion creates a fusion between the 5' end of MOZ mRNA and the 3' end of TIF2 mRNA maintaining the translational frame of the protein. The predicted fusion protein contains the zinc finger domains, the nuclear localization domains, the histone acetyltransferase (HAT) domain, and a portion of the acidic domain of MOZ, coupled to the CREB-binding protein (CBP) interaction domain and the activation domains of TIF2. The breakpoint is distinct from the breakpoint in the t(8;16)(p11;p13) translocation in acute monocytic leukemia with erythrophagocytosis that fuses MOZ with CBP. The reciprocal TIF2-MOZ fusion gene is not expressed, perhaps as a result of a deletion near the chromosome 8 centromere. The MOZ-TIF2 fusion is one of a new family of chromosomal rearrangements that associate HAT activity, transcriptional coactivation, and acute leukemia.
急性白血病中的染色体异常已促使人们发现了许多参与正常造血和恶性转化的基因。我们已在一名急性混合谱系白血病患者的inv(8)(p11q13)中鉴定出融合伙伴。我们通过荧光原位杂交(FISH)分析、Southern印迹和逆转录聚合酶链反应(RT-PCR)表明,MOZ(单核细胞白血病锌指蛋白)基因和TIF2(转录中介因子2)基因参与了inv(8)(p11q13)。我们证明这种倒位在MOZ mRNA的5'端和TIF2 mRNA的3'端之间产生了融合,从而维持了蛋白质的翻译框架。预测的融合蛋白包含锌指结构域、核定位结构域、组蛋白乙酰转移酶(HAT)结构域以及MOZ酸性结构域的一部分,与CREB结合蛋白(CBP)相互作用结构域和TIF2的激活结构域相连。该断点与伴有噬红细胞现象的急性单核细胞白血病中t(8;16)(p11;p13)易位的断点不同,后者使MOZ与CBP融合。相互的TIF2-MOZ融合基因未表达,可能是由于8号染色体着丝粒附近的缺失所致。MOZ-TIF2融合是将HAT活性、转录共激活与急性白血病联系起来的一个新的染色体重排家族之一。