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应用限制性显示技术制备HCV cDNA诊断基因芯片的初步研究
引用本文:孙朝晖 郑文岭 彭翼飞 张宝 马文丽. 应用限制性显示技术制备HCV cDNA诊断基因芯片的初步研究[J]. 微生物学报, 2005, 45(2): 226-230
作者姓名:孙朝晖 郑文岭 彭翼飞 张宝 马文丽
作者单位:1. 南方医科大学基因工程研究所,广州,510515;广州军区广州总医院肿瘤分子生物学研究所,广州,510010
2. 广州军区广州总医院肿瘤分子生物学研究所,广州,510010
3. 南方医科大学基因工程研究所,广州,510515
基金项目:国家自然科学基金 (3 9880 0 3 2 ),广州市重大科技攻关项目 (0 1_Z_0 0 5_0 1)~~
摘    要:制备丙型肝炎病毒 (HCV)检测芯片并进行验证、初步检测质量评价。采用限制性显示 (Restrictiondisplay ,RD)技术制备芯片探针 ,从载体pCV_J4L6S中切出HCV全长cDNA ,Sau3AⅠ酶消化 ,所得的限制性片段进行RD_PCR扩增 ,经聚丙烯酰胺电泳 (PAGE)结合银染法进行分离。切胶回收后作 3次PCR ,得到较纯净的HCVcDNA限制性片段。扩增后的产物克隆至pMD18_T载体进行快速鉴定。将筛选出的限制性片段打印在氨基修饰的玻片上制备成检测芯片进行杂交验证分析 ,对芯片检测进行优化、初步的质量评估。运用RD技术 ,得到 2 4个 2 0 0~ 80 0bp、大小均一的基因片段 ,序列分析表明 ,均属于HCV特异基因 ,可以作为诊断芯片探针 ;杂交、测序结果显示 ,芯片检测的敏感性、特异性、准确度、重复性、线性等指标均佳。利用RD技术制备基因芯片探针是一种快速、简便的实用方法 ;制备的诊断芯片可以用于检测HCVRNA ,具有敏感、检测结果较为可靠的优点。

关 键 词:丙型肝炎病毒  限制性显示  分子探针  基因芯片  杂交  诊断
文章编号:0001-6209(2005)02-0226-05
修稿时间:2004-05-25

Research of restriction display technique in cDNA microarrays preparation for detecting of HCV
SUN Zhao-hui,ZHENG Wen-ling,PENG Yi-fei,ZHANG Bao,MA Wen-li. Research of restriction display technique in cDNA microarrays preparation for detecting of HCV[J]. Acta microbiologica Sinica, 2005, 45(2): 226-230
Authors:SUN Zhao-hui  ZHENG Wen-ling  PENG Yi-fei  ZHANG Bao  MA Wen-li
Affiliation:Institute of Genetic Engineering, Southern Medical University, Guangzhou 510515, China. zhaohui2@fimmu.com
Abstract:The cDNA microarrays for HCV detection was prepared. With the restriction display technique (RD), restriction enzyme Sau3A I was chosen to digest the full-length HCV cDNAs. The products were classified and amplified by RD-PCR. We separated the differential genes through polyacrylamide gel electrophoresis and sliver staining. Single bands were isolated which were cut out from the polyacrylamide gel. The third-round PCR could be performed by using the single bands as PCR template. The RD-PCR fragments were purified and cloned into the pMD18-T vectors. The recombinant plasmids were extracted from positive clones and the target gene fragments were sequenced. The cDNA microarray was prepared by spotting PCR products to the surface of amido modified glass slides by the robotics. We validated the detection of microarray by the hybridization and the results of sequence analysis. A total of 24 different cDNA fragments ranging from 200 to 800 bp were isolated and sequenced, which were the specific gene fragments of HCV. These fragments could be further used as probes in the microarray preparations. From the results of hybridization and sequence date analysis, the specificity, sensitivity, accuracy, reproducibility and linearity in detecting HCV RNA were satisfactory. RD technique is of great value in obtaining a large number of size-comparable gene probes, which provide a swift protocol in generating probes for the preparation of microarrays, and the optimized microarray is sensitive and effective in clinical diagnosis of HCV.
Keywords:Restriction display   HCV   Gene probes   Microarray   Hybridization   Diagnosis
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