Gene expression of PROSC (proline synthetase co-transcribed) in related to cytosine arabinoside sensitivity in human leukemia

S. Fujimaki, Mayu Takeda, Kuniaki Saito, T. Funato
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Abstract

We examined the PCR differential display analysis of cDNA clones from human leukemia K562 cell line and those of cytosine arabinoside (ara-C) resistant K562 cells. We compared mRNA samples obtained from the two cell lines by amplified restriction fragment length polymorphism (AFLP)-based mRNA fingerprinting; 40 bands were observed in each lane of a gel, and the screened results were five independent, isolated clones. In this study, we isolated the proline synthetase co-transcribed (PROSC) gene from an ara-C sensitive K562 cell line as one of the clones. RNase protection assay and RT-PCR analysis revealed increased expression of PROSC gene in K562 sensitive cells compared with that of ara-C resistant K562 cells. The PROSC gene product is likely a soluble cytoplasmic protein, but its function remains unclear. Thus, the PROSC gene might be related to the sensitivity to ara-C in human leukemia and downregulated in resistant cells.
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PROSC(脯氨酸合成酶共转录)基因表达与人白血病中阿糖胞嘧啶敏感性相关
我们检测了人白血病K562细胞系cDNA克隆与阿拉伯糖胞嘧啶(ara-C)抗性K562细胞cDNA克隆的PCR差异显示分析。我们通过扩增限制性片段长度多态性(AFLP)的mRNA指纹技术比较了两种细胞系的mRNA样本;在凝胶的每条通道中观察到40条条带,筛选结果为5个独立的分离克隆。本研究从ara-C敏感细胞系K562中分离出脯氨酸合成酶共转录(PROSC)基因作为克隆之一。RNase保护实验和RT-PCR分析显示,与ara-C抗性K562细胞相比,K562敏感细胞中PROSC基因的表达增加。PROSC基因产物可能是一种可溶性细胞质蛋白,但其功能尚不清楚。因此,PROSC基因可能与人白血病对ara-C的敏感性有关,并在耐药细胞中下调。
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