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应用抑制消减杂交技术筛选动脉粥样硬化相关基因
引用本文:山丽梅,张锦超,崔文玉,俞炜源,汪海.应用抑制消减杂交技术筛选动脉粥样硬化相关基因[J].中国药理学与毒理学杂志,2004,18(5):371-378.
作者姓名:山丽梅  张锦超  崔文玉  俞炜源  汪海
作者单位:1. 中国人民解放军第302医院药学部,北京,100039
2. 军事医学科学院生物工程研究所,北京,100071
3. 军事医学科学院毒物药物研究所,北京,100850
基金项目:国家重点基础研究发展计划(973计划)
摘    要:目的 筛选动脉粥样硬化 (AS)相关基因。方法通过菌落原位杂交技术筛选用抑制消减杂交法构建的传代培养前后牛主动脉内皮细胞差异表达基因消减cDNA文库 ,用聚合酶链反应方法进一步筛选出有插入片段的阳性克隆 ,将阳性克隆进行DNA测序和同源性比较分析。建立兔AS模型 ,采用RNA点杂交技术鉴定部分筛选到的cDNA序列的AS相关性。结果 从消减文库中随机挑取的 75 0个白色克隆中筛选出 88个阳性克隆 ,DNA测序获得 6 1个cDNA序列 ,其中 2 6个为已知牛基因序列 ,19个与已知人基因具有高度同源性 ,其他 16个是未知基因片段。通过基因同源性分析 ,选择部分cDNA序列进行组织表达差异及其与AS病变的关系分析 ,结果表明 ,转录调节因子DEAD box ,Ⅻa因子抑制蛋白 ,淋巴调适蛋白和转位复合蛋白 β基因为AS相关基因。结论 这 4种基因为本文首次报道的AS相关基因。

关 键 词:动脉粥样硬化  内皮  血管  细胞  培养的  主动脉  抑制消减杂交
收稿时间:2003-12-12

Screening of atherosclerosis related genes using suppression subtractive hybridization technique
SHAN Li-Mei, ZHANG Jin-Chao, CUI Wen-Yu, YU Wei-Yuan, WANG Hai.Screening of atherosclerosis related genes using suppression subtractive hybridization technique[J].Chinese Journal of Pharmacology and Toxicology,2004,18(5):371-378.
Authors:SHAN Li-Mei  ZHANG Jin-Chao  CUI Wen-Yu  YU Wei-Yuan  WANG Hai
Institution:(1. Department of Pharmacy, 302 Hospital of PLA, Beijing 100039, China; 2. Institute of Biotechnology, Beijing 100071, China; 3. Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China)
Abstract:AIM To screen the atherosclerosis related genes. METHODS The differentially expressed subtracted cDNA library of freshly isolated adult bovine endothelium and cultured new-born bovine endothelium constructed by suppression subtractive hybridization technique was screened by colony in situ hybridization, the positive clones were further screened with PCR amplification. The positive clones were sequenced and analyzed for homology in the GenBank databases with basic local alignment search tool. The atherosclerosis related genes were analyzed by RNA dot-blot analysis on rabbit atherosclerosis model. RESULTS Eighty-eight positive clones were obtained, and 61 cDNA sequences were identified. Sequences of 61 cDNA showed that 26 cDNA were known as bovine gene sequences, 19 cDNA were homologous with the human genes published in GenBank and 16 cDNA were unknown genes. Through gene homologous analysis, some differentially expressed cDNA sequences were selected for tissue differential and atherosclerosis related analysis. We found that DEAD-box protein, factor Ⅻa inhibitor, lymphocyte adaptor protein and protein translocation complex β are all atherosclerosis related genes. CONCLUSION This is the first time to report four genes are related to atherosclerosis.
Keywords:atherosclerosis  endothelium  vascular  cells  cultur ed  aorta  suppression subtractive hybridization
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