首页> 外文期刊>Journal of neuro-oncology. >Isolation of novel differentially expressed genes related to human glioma using cDNA microarray and characterizations of two novel full-length genes.
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Isolation of novel differentially expressed genes related to human glioma using cDNA microarray and characterizations of two novel full-length genes.

机译:使用cDNA微阵列分离与人类神经胶质瘤相关的新的差异表达基因,并鉴定两个新的全长基因。

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Identification of the genes that are differentially expressed between brain tumor and normal brain tissues is important for understanding the molecular basis of these nerve system tumors and for defining possible targets for therapeutic intervention. This investigation is intended to obtain differentially expressed genes related to human glioma using cDNA microarray. Total RNA was extracted from human glioma specimens and normal brain tissues, and mRNA was obtained by oligotex chromatography. The cDNA microarray contains 4366 novel cDNA clones. The results of hybridization were scanned using computer system. Two genes selected from the results of cDNA microarray hybridization were subsequently analyzed by bio-informatic approach, Northern blot, in situ hybridization and radiation hybridization. We demonstrated that at a differentially expressed ration of two to three times, 15 cDNA clones were considered differentially expressed. Two novel full-length genes were selected for further investigation, one named human PKIbeta gene (clone 436F11, GenBank with accession number: AF225513) was over-expressed in normal brain tissues and the other named human ribosomal protein L14.22 gene (clone 507E08, GenBank with accession number: AF329277) was over-expressed in gliomas. Furthermore, the 436F11 gene was located on 6q21-q23 between the D6S304 and D6S2156 markers, while the 507E08 gene was located between the D14S1066 and D14S265 markers. We realized that cDNA microarray technology can be successfully applied to identify differentially expressed genes in human glioma. This approach is superior to routine representational difference analysis, suppression subtractive hybridization and Northern blot for detection and isolation of differentially expressed genes in different tissues. At present, we have discovered two novel full-length genes related to human glioma and their characterizations have been partially clarified.
机译:鉴定在脑肿瘤与正常脑组织之间差异表达的基因对于理解这些神经系统肿瘤的分子基础以及确定治疗性干预的可能靶点很重要。这项研究旨在使用cDNA微阵列获得与人神经胶质瘤相关的差异表达基因。从人脑胶质瘤标本和正常脑组织中提取总RNA,并通过寡聚层析获得mRNA。 cDNA微阵列包含4366个新的cDNA克隆。杂交结果用计算机系统扫描。随后通过生物信息学方法,Northern印迹,原位杂交和放射杂交分析了从cDNA微阵列杂交结果中选择的两个基因。我们证明了差异表达比率为2至3倍,认为15个cDNA克隆差异表达。选择了两个新的全长基因进行进一步研究,其中一个名为人PKIbeta基因(克隆436F11,GenBank,登录号:AF225513)在正常脑组织中过表达,另一个名为人核糖体蛋白L14.22基因(克隆507E08)。 ,GenBank,登录号:AF329277)在神经胶质瘤中过表达。此外,436F11基因位于D6S304和D6S2156标记之间的6q21-q23上,而507E08基因位于D14S1066和D14S265标记之间。我们意识到,cDNA微阵列技术可以成功地应用于鉴定人神经胶质瘤中差异表达的基因。这种方法优于常规的代表性差异分析,抑制消减杂交和Northern印迹法,用于检测和分离不同组织中差异表达的基因。目前,我们发现了两个与人类神经胶质瘤有关的新型全长基因,其特征已经部分阐明。

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