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首页> 外文期刊>Genes, Chromosomes and Cancer >Expression analysis of genes located in the minimally deleted regions of 13q14 and 11q22-23 in chronic lymphocytic leukemia-unexpected expression pattern of the RHO GTPase activator ARHGAP20.
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Expression analysis of genes located in the minimally deleted regions of 13q14 and 11q22-23 in chronic lymphocytic leukemia-unexpected expression pattern of the RHO GTPase activator ARHGAP20.

机译:位于慢性淋巴细胞性白血病的13q14和11q22-23最小缺失区域中的基因的表达分析-RHO GTPase激活剂ARHGAP20的异常表达模式。

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摘要

In chronic lymphocytic leukemia (CLL), 13q14 and 11q22-23 deletions are found in 2/3 of the cases. 11q22-23 deletions are associated with poor survival, whereas 13q14 deletions as single abnormality are often found in indolent disease forms. The molecular basis for this difference in prognosis is not known. We examined the 13q14 and 11q22-23 minimally deleted regions (MDRs) for differentially expressed genes by analyzing 154 microarray CLL gene expression data sets. We were able to generate a detailed gene expression map of the MDRs demonstrating a gene dosage effect. Surprisingly, ARHGAP20 encoding the RHO GTPase activating protein 20, which is located in the 11q22-23 MDR, showed-counterintuitively-a significantly higher expression in cases with 11q22-23 deletions compared with cases with no detectable genetic lesion or trisomy 12. Interestingly, cases with 13q14 deletions also had higher ARHGAP20 expression. These expression level changes were confirmed by quantitative PCR in 110 additional CLL samples. The ARHGAP20 gene encodes an evolutionarily conserved protein. In the zebra fish (Danio rerio) genome the syntenic regions of human chromosomal bands 13q14 and 11q22-23 are juxtaposed. The similar expression profiles of ARHGAP20 in 13q14 and 11q22-23 deleted CLL cases suggest a molecular connection and an intriguing mechanism of regulation.
机译:在慢性淋巴细胞性白血病(CLL)中,在2/3的病例中发现13q14和11q22-23缺失。 11q22-23缺失与较差的生存率相关,而13q14缺失则作为单一异常常在惰性疾病形式中发现。这种预后差异的分子基础尚不清楚。我们通过分析154个微阵列CLL基因表达数据集,检查了13q14和11q22-23最小缺失区(MDR)的差异表达基因。我们能够生成MDR的详细基因表达图谱,表明基因剂量效应。令人惊讶的是,位于11q22-23 MDR中的编码RHO GTPase活化蛋白20的ARHGAP20与非可检测的遗传病灶或三体性疾病相比,具有11q22-23缺失的患者表达明显高于直觉。具有13q14缺失的病例也具有更高的ARHGAP20表达。这些表达水平的变化通过定量PCR在另外110个CLL样品中得到证实。 ARHGAP20基因编码一种进化保守的蛋白质。在斑马鱼(Danio rerio)基因组中,人染色体带13q14和11q22-23的同音区域并列。 ARHGAP20在13q14和11q22-23缺失的CLL病例中的相似表达谱提示分子连接和有趣的调控机制。

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