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作 者:徐学明[1] 傅敏庄[1] 王葆春[1] 朱定尔[1]
机构地区:[1]湖南医科大学分子生物学研究室
出 处:《生物化学杂志》1996年第6期659-663,共5页
摘 要:应用竞争性逆转录聚合酶链式反应(RT-PCR)测定了10例急性粒细胞白血病M_2型(AML)患者外周血网织红细胞中α/β珠蛋白mRNA的相对含量,其中8例表现不同程度增高,2例正常,均值为1.513±0.182(±s),与正常对照组(1.24±0.083)进行t检验比较,有非常显著差异(P<0.01).此外,PCR-SSCP分析显示AML患者β珠蛋白基因启动子区序列(5'端-135至+122位核苷酸)无明显异常。说明AML患者珠蛋白基因表达失衡系由于转录异常,很可能系AML的发生对α/β珠蛋白基因的平衡表达产生了某种影响,从而表现为获得性β地中海贫血特征。实验结果为进一步探讨白血病的发病机理及其α/β珠蛋白基因表达失衡的机制奠定了基础。The relative amounts of α/β globin mRNA ratio (α/βmRNA ratios) in peripheral reticulocytes from the patients with acute myeloid leukemia (AML) was quantitated by the reverse transcription-polymerase chain reaction(RT-PCR) techniques. The α/β mRNA ratios in ten patients with AML were determined to be 1. 513 ±0 . 182 ( mean ±SD), while those in normal group is 1.214±0 .083, the α/β mRNA ratios in AML patients differ from those in normal control with very significant difference (P<0.01) . The disequilibrium of α/β globin chain biosynthesis in different types of leukemia had been reported already by our laboratory before. The above results showed that the disequilibrium of globin biosynthesis in AML may be caused by the disturbance of globin gene expression. The characteristics of the expression of α/β globin genes in AML is similar to that in β-thalassemia and is called as'Acquired β-thalassemia' here, the mechanism of which is still unknown, and needs to be further studied in order to elucidate the pathogenesis of leukemia,as well as the regulation of the globin gene expression in leukemia.
分 类 号:R733.710.2[医药卫生—肿瘤]
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