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作 者:祁震宇[1] 惠国桢[1] 李瑶[2] 周宗祥[2] 应康[2] 谢毅[2]
机构地区:[1]苏州大学附属第一医院神经外科,215006 [2]上海复旦大学遗传工程国家重点开放实验室
出 处:《中华实验外科杂志》2005年第7期849-851,i002,共4页Chinese Journal of Experimental Surgery
摘 要:目的运用基因芯片技术获取正常成人脑组织与人脑胶质瘤中差异表达的基因,并对其中一条基因进行了初步的研究。方法抽提正常成人脑组织与人脑胶质瘤组织中的mRNA来制备探针,经杂交、洗涤后,通过计算机观察两者表达谱的差异情况,对681F05克隆子进行了Northernblot,5’RACE和生物信息学分析。结果通过4次基因芯片筛选,获得15条与胶质瘤相关的新基因,经Northernblot证实681F05基因在人正常脑组织中低表达,而在人脑胶质瘤中高表达。BLASTn和BLASTx分析显示,它们编码蛋白与线虫Cyp10蛋白同源性分别为52%和72%。cDNA序列分析发现这两上克隆是同一个基因[命名为cyclophilinlikegene(PPIL3)]的两个不同的剪切体(PPIL3a和PPIL3b)。结论基因芯片筛选正常脑组织与人脑胶质瘤差异表达的基因具有样品用量少,高质量,高速度,高敏感等特性。681F05基因可能是与人脑胶质瘤形成有关的一条全长新基因。Objective To obtain differentially expressed genes related to human glioma using cDNA microarray and evaluate the characterization of one novel full-length gene.Methods Total RNA was extracted from human glioma tissues and normal brain tissues,and mRNA was used to make probes.After hybridization and washing procedure,the results of hybridization were scanned using computer system.One gene named 681F05 clone was subsequently analyzed by Northern blot,5'RACE and bioinformatics.Results Fifteen differentially expressed genes to human glioma were obtained through 4 times hybridizations and scanning.Northern blot analysis confirmed 681F05 clone was low-expressed in human brain tissue and overexpressed in human glioma tissues.The analysis of BLASTn and BLASTx showed that the isolated clone 681F05 was two cDNA clones encoding two novel proteins which showed 52% and 72% identity to the cyclophilin isoform 10 of C.Elgans,respectively.Sequence analysis revealed these two cDNA clones were two different splicing variants of a novel cycophilin-like gene (PPIL3a and PPIL3b).Conclusion cDNA microarray technology can be successfully applied to identify differentially expressed genes.The novel full-length gene of human PPIL3 may by correlate with pathogenesis of human glioma.
关 键 词:全长新基因 差异表达 克隆 CDNA序列分析 人脑胶质瘤组织 生物信息学分析 Northem 正常脑组织 基因芯片技术 人脑组织 blot mRNA RACE 编码蛋白 表达谱 计算机 低表达 高表达 同源性 剪切体 筛选
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