首页> 外文期刊>Human Genetics >Structure and mutation analysis of the gene encoding DNA fragmentation factor 40 (caspase-activated nuclease), a candidate neuroblastoma tumour suppressor gene.
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Structure and mutation analysis of the gene encoding DNA fragmentation factor 40 (caspase-activated nuclease), a candidate neuroblastoma tumour suppressor gene.

机译:编码DNA片段化因子40(胱天蛋白酶激活的核酸酶)(一种候选神经母细胞瘤抑癌基因)的基因的结构和突变分析。

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摘要

We have characterised the DFFB gene, encoding the active subunit of the apoptotic nuclease DNA fragmentation factor (DFF40). DFFB maps to 1p36, near the imprinted putative tumour suppressor gene TP73. The DFFA gene (encoding the inhibitory DFF45 subunit) also maps to 1p36.2-36.3, and we show by FISH that DFFB lies distal to DFFA. We have also mapped a processed DFFB pseudogene to chromosome 9. DFFB itself has seven coding exons spanning 10 kb. Exhaustive mutation screening of 41 neuroblastomas and other tumours in which a 1p36 tumour suppressor gene is implicated showed no tumour-specific mutations. A coding region polymorphism was used to demonstrate uniformly biallelic expression in human fetal DFFB transcripts. Since the putative neuroblastoma tumour suppressor gene in distal 1p36 is predicted to be maternally expressed, the lack of imprinting and absence of somatic mutations in DFFB indicate that it is probably not the neuroblastoma tumour suppressor gene.
机译:我们已经表征了DFFB基因,其编码凋亡核酸酶DNA片段化因子(DFF40)的活性亚基。 DFFB映射到印迹的假定抑癌基因TP73附近的1p36。 DFFA基因(编码抑制性DFF45亚基)也映射到1p36.2-36.3,我们通过FISH显示DFFB位于DFFA的远端。我们还将一个处理过的DFFB假基因映射到9号染色体。DFFB本身具有七个编码外显子,跨度10 kb。对涉及1p36抑癌基因的41个神经母细胞瘤和其他肿瘤进行详尽的突变筛选,未发现肿瘤特异性突变。使用编码区多态性来证明人类胎儿DFFB转录本中的均匀双等位基因表达。由于预计在远端1p36假定的神经母细胞瘤抑癌基因在母亲中表达,DFFB中印迹的缺乏和体细胞突变的缺乏表明它可能不是神经母细胞瘤抑癌基因。

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