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首页> 外文期刊>FEBS Letters >Characterization of a novel B‐CLL candidate gene – DLEU7 – located in the 13q14 tumor suppressor locus
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Characterization of a novel B‐CLL candidate gene – DLEU7 – located in the 13q14 tumor suppressor locus

机译:位于13q14肿瘤抑制基因座的新型B-CLL候选基因DLEU7的特征

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>Deletion of chromosome 13q14 is the most frequent genetic aberration in B-cell chronic lymphocytic leukemia (CLL), found in more than 50% of cases, indicating that this region contains a gene(s) involved in the development of CLL. However, the pathogenic gene in the critical 13q14 region has not yet been defined. Here, we have cloned and characterized a novel gene, DLEU7, located adjacent to the consensus deleted region, and overlapping the 3′ end of DLEU1 tail to tail. Human DLEU7 encodes a putative 221 amino acid protein, with significant conservation in rodents. Mutational and expression analysis in primary CLL samples failed to demonstrate any specific mutations in DLEU7, but no DLEU7 expression could be detected in CLL cells. Methylation of a CpG island in the promoter region of DLEU7 was further analyzed as a possible mechanism for the absence of DLEU7 expression, and the promoter was found to be methylated in the majority of the CLL samples investigated.
机译:>删除13q14染色体是B细胞慢性淋巴细胞性白血病(CLL)中最常见的遗传畸变,在50%以上的病例中发现,表明该区域包含一个参与CLL发生的基因。但是,尚未确定13q14关键区域的致病基因。在这里,我们克隆并鉴定了一个新的基因 DLEU7 ,它位于共有缺失区域附近,并与 DLEU1 的3'端尾对尾重叠。人 DLEU7 编码一种假定的221个氨基酸的蛋白质,在啮齿动物中具有明显的保守性。原代CLL样品的突变和表达分析未能证明 DLEU7 中有任何特定突变,但在CLL细胞中未检测到 DLEU7 表达。作为 DLEU7 表达缺失的可能机制,进一步分析了 DLEU7 启动子区域中CpG岛的甲基化,发现该启动子多数被甲基化被调查的CLL样本。

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