首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Cloning, sequencing and expression analysis of a novel gene BR-1 that is expressed in normal human brain tissue but not in glioma tumor samples.
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Cloning, sequencing and expression analysis of a novel gene BR-1 that is expressed in normal human brain tissue but not in glioma tumor samples.

机译:在正常人脑组织中表达但在神经胶质瘤肿瘤样品中不表达的新型基因BR-1的克隆,测序和表达分析。

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摘要

Using the technique of differential hybridization of a human fetal brain library, we identified a novel gene, brain 1 (BR-1). This gene is expressed in normal brain but has low or no expression in human gliomas. We have cloned and sequenced the full-length cDNA corresponding to this gene. A data base search for the nucleotide sequence homology was performed for BR-1. The BR-1 sequence showed strong homology to a human genomic clone from chromosome 2. Moderate sequence homology was observed between BR-1 and an expressed sequence tag (EST) from a human placenta library. Three different regions of BR-1 also showed homology to a mouse EST that is similar to EL-10 gene. Sequence analysis indicated that the protein sequence for BR-1 has one tyrosine kinase phosphorylation site and two N-myristoylation sites. Northern blot analysis indicated that the BR-1 gene is expressed in heart, placenta, lung, liver, skeletal muscle, kidney and pancreas. A low level of expression of BR-1 is observed in the cerebellum, cerebral cortex, spinal cord, occipital lobe and putamen. The BR-1 gene is also expressed in fetal brain, liver and kidney. Low expression of BR-1 gene was observed in a number of non-brain tumor cell lines. RT-PCR analysis indicated that the BR-1 gene was expressed in non-neoplastic (epilepsy specimens) but not in six oligodendrogliomas and three oligoastrocytoma tumor samples analyzed. BR-1 was not expressed in either seven low grade gliomas or eight grade IV glioblastoma tumor tissue samples analyzed. Three glioblastoma cell lines did show low expression of the BR-1 gene. On the basis of its expression properties, we conclude that BR-1 is a potential novel tumor suppressor gene.
机译:使用人类胎儿大脑文库的差异杂交技术,我们鉴定了一个新基因,大脑1(BR-1)。该基因在正常脑中表达,但在人脑胶质瘤中表达低或不表达。我们已经克隆并测序了与该基因相对应的全长cDNA。对BR-1进行了核苷酸序列同源性的数据库搜索。 BR-1序列与来自2号染色体的人类基因组克隆显示出强烈的同源性。在BR-1与人类胎盘文库的表达序列标签(EST)之间观察到中等的序列同源性。 BR-1的三个不同区域也显示出与小鼠EST的同源性,类似于EL-10基因。序列分析表明BR-1的蛋白质序列具有一个酪氨酸激酶磷酸化位点和两个N-肉豆蔻酰化位点。 Northern印迹分析表明,BR-1基因在心脏,胎盘,肺,肝,骨骼肌,肾脏和胰腺中表达。在小脑,大脑皮层,脊髓,枕叶和壳状核中观察到BR-1的低水平表达。 BR-1基因也在胎儿脑,肝和肾中表达。在许多非脑肿瘤细胞系中观察到BR-1基因的低表达。 RT-PCR分析表明,BR-1基因在非肿瘤(癫痫标本)中表达,但在分析的6个少突胶质细胞瘤和3个少突胶质细胞瘤样品中不表达。在分析的7个低度神经胶质瘤或8个IV级胶质母细胞瘤肿瘤组织样品中均未表达BR-1。三种胶质母细胞瘤细胞系确实显示出BR-1基因的低表达。根据其表达特性,我们得出结论,BR-1是潜在的新型抑癌基因。

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