Sasaki Osamu, Meguro Kuniaki, Tohmiya Yasuo, Funato Tadao, Shibahara Shigeki, Sasaki Takeshi
Department of Rheumatology and Hematology, Tohoku University School of Medicine, Sendai, Japan.
Br J Haematol. 2002 Dec;119(4):940-8. doi: 10.1046/j.1365-2141.2002.03972.x.
The retinoblastoma protein-interacting zinc finger gene (RIZ), a member of the nuclear protein methyltransferase superfamily, is characterized by the presence of the N-terminal PR domain. The RIZ gene encodes for two proteins, RIZ1 and RIZ2. While RIZ1 contains the PR (PRDI-BF1 and RIZ homologous) domain, RIZ2 lacks it. RIZ gene expression is altered in a variety of human cancers and RIZ1 is now considered to be a candidate tumour suppressor. To investigate the role of RIZ in leukaemogenesis, we analysed the differential expression of RIZ1 and RIZ2 by quantitative real-time reverse-transcription polymerase chain reaction assay. Our results showed that the expression of RIZ1 was significantly decreased in leukaemia cell lines (14 out of 17, 82%) and in patients with acute myeloblastic leukaemia (eight out of 14, 57%). In contrast, RIZ2 expression was increased in patients with acute lymphoblastic leukaemia (eight out of 11, 73%), compared with normal bone marrow cells. These findings indicate that suppression of RIZ1 expression or enhancement of RIZ2 expression may have an important role in leukaemogenesis.
视网膜母细胞瘤蛋白相互作用锌指基因(RIZ)是核蛋白甲基转移酶超家族的成员,其特征是存在N端PR结构域。RIZ基因编码两种蛋白质,即RIZ1和RIZ2。RIZ1含有PR(PRDI-BF1和RIZ同源)结构域,而RIZ2则没有。RIZ基因的表达在多种人类癌症中发生改变,RIZ1现在被认为是一种候选肿瘤抑制因子。为了研究RIZ在白血病发生中的作用,我们通过定量实时逆转录聚合酶链反应分析了RIZ1和RIZ2的差异表达。我们的结果表明,RIZ1的表达在白血病细胞系(17个中有14个,82%)和急性髓细胞白血病患者(14个中有8个,57%)中显著降低。相比之下,与正常骨髓细胞相比,急性淋巴细胞白血病患者(11个中有8个,73%)中RIZ2的表达增加。这些发现表明,RIZ1表达的抑制或RIZ2表达的增强可能在白血病发生中起重要作用。