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鼻咽癌细胞中表达上调的新基因NAG23(FBXO30)的克隆与分析 被引量:6

Molecular Cloning and Analysis of a Novel Gene, NAG23 (FBXO 30),Upregulated in Nasopharyngeal Carcinoma
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摘要 目的:分离位于6号染色体长臂鼻咽癌高频等位基因不平衡位点D6S1581(6q25.3-27)附近与鼻咽癌相关的新基因。方法:运用差异RT-PCR检测定位于D6S1581附近的11个表达序列标签(expressedsequencetags,EST)在正常人鼻咽上皮细胞和鼻咽癌细胞系中的表达水平,并对其中一个表达上调的EST在鼻咽癌组织和正常鼻咽组织中的表达情况进行分析。用Northern杂交验证其表达差异并检测其在多脏器中的表达及其所代表基因的转录本大小。利用生物信息学资源克隆并获得其全长cDNA,对该序列进行初步分析。结果:获得了一个位于6q25.3-27的在鼻咽癌中表达上调的新基因,命名为NAG23(FBXO30)(GenBank收录编号:AF248640)。该基因在68.9%的鼻咽癌活检组织中表达上调,cDNA全长3301bp,预测其开放阅读框编码一个含390个氨基酸的胞浆蛋白,该蛋白含一个F-box基序。结论:NAG23基因是一个在鼻咽癌中表达上调的新基因,很可能编码一新的F-box蛋白。NAG23可能参与了鼻咽癌的发生发展。 Objective: The aim of this study was to seek novel genes associated with human nasopharyngeal carcinoma (NPC) around the microsatellite D6S1581 with high frequency of allelic imbalance in NPC tissues at the long arm of chromosome 6q25.3-27. Methods: Eleven epithelial derived expressed sequence tags (EST) were selected from the region around D6S1581. Differential RT PCR was applied to detect the expression of these EST in NPC cell line, HNE1, and the primary cultures of normal nasopharyngeal epithelial cells. Then, expression of EST AI536544 was further detected in 3 normal nasopharyngeal biopsies and 29 NPC biopsies by differential RT PCR. By Northern blots, the differential expression of the EST AI536544 was confirmed, the expression of the EST in the human eight tissues and the size of the transcript of the EST representative gene were also determined. The putative full length cDNA of the EST representative gene was cloned and the sequence of the novel gene was analyzed by bioinformatics. Results: EST AI536544 was overexpressed in the NPC cell line, HNE1, and in 68.9% of NPC biopsies. The full length cDNA with no homology to any reported genes in the database of GenBank was obtained and named NAG23 (FBXO 30)(GenBank accession number, AF248640), which is located around D6S1581(6q25.3-27).A 390 amino acid cytoplasm protein with a F box motif was deduced from the potential open reading frame of the 3301bp full length cDNA. Conclusion: NAG23 is a novel gene upregulated in NPC, which likely encode an F box protein and may be involved in development of NPC.
出处 《癌症》 SCIE CAS CSCD 北大核心 2001年第9期906-910,共5页 Chinese Journal of Cancer
基金 国家"863"项目(项目编号:102-10-01-05) 国家"973"重点项目(项目编号:G1998051008)
关键词 鼻咽肿瘤 基因克隆 F-BOX蛋白 NAG23基因 Nasopharyngeal neoplasma Gene cloning F box protein
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  • 1Sun Y,Proc Natl Acad Sci USA,1992年,89卷,6516页
  • 2朱丹,中华医学遗传学杂志,1994年,11卷,354页
  • 3Ji H J,Cancer Res,1997年,57卷,3期,759页
  • 4Sun Y,Can J,1995年,8卷,6期,325页
  • 5陈孝光,中国科学技术协会中国科协首界青年学术论文集,1992年,48页
  • 6Yao K T,Int J Cancer,1992年,45卷,1期,83页
  • 7Liang P,Science,1992年,257卷,5072期,967页
  • 8Li G Y,Chin J Cancer Res,1991年,3卷,1期,31页
  • 9Zhang S Z,Hereditas,1982年,97卷,1期,23页
  • 10姚开泰,湖南医学院学报,1982年,7卷,1期,10页

共引文献32

同被引文献47

  • 1胡维新,曹亚,李晓艳,姚开泰.Tx基因与IgK基因的同源性研究及其在不同细胞株的表达[J].生物化学与生物物理学报,1995,27(2):215-221. 被引量:16
  • 2黄剑,唐慰萍,姚运红,李飞虹,李岩松.C-erbB-2癌基因产物在良恶性鼻咽组织及鼻咽癌细胞系和克隆株中的表达[J].癌症,1996,15(4):256-258. 被引量:9
  • 3曹亚 孙毅 等.对鼻咽癌恶性转化基因Tx表达的初步研究[J].生物化学杂志,1995,11(4):381-385.
  • 4胡利富 蒋金荃 李晓林 等.人鼻咽癌癌基因Ha-ras[J].癌症,1988,7(4):251-254.
  • 5Sambrook J 等 金冬雁等(译).分子克隆实验指南,第2版[M].北京:科学出版社,1992.880-898.
  • 6Yang T T,Nucl Acids Res,1996年,24卷,4592页
  • 7金冬雁(译),分子克隆实验指南(第2版),1992年,880页
  • 8Muir C,Waterhouse J,Mack T,et al.Cancer in cidence in five continents.In:International Agency for Research on Cancer.IARC Scientific Publication No.88,1987,5.Lyon,France:International Agency for Research on Cancer,1987.1 ~970.
  • 9Huang D P,Lo K W,Choi P H,et al.Loss of heterozygosity on the short arm of chromosome 3 in nasopharyngeal carcinoma.Cancer Genet Cytogenet,1991,54 (1):91 ~99.
  • 10Zhou J,Ma J,Zhang B C,et al.BRD7,a novel bromodomain gene,inhibits G1-S progression by transcriptionally regulating some important molecules involved in ras/MEK/ERK and Rb/E2F pathways.J Cell Physiol,2004,200 (1):89~98.

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