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作 者:于永生[1,2] 罗晓彤[1] 金海国[1] 任刚[2] 胡士军[2]
机构地区:[1]吉林省农业科学院畜牧分院,吉林公主岭136100 [2]东北农业大学生命科学院,哈尔滨150030
出 处:《中国农业大学学报》2009年第3期22-26,共5页Journal of China Agricultural University
基 金:国家“973”计划项目(2006CB504005)
摘 要:利用microRNA靶位点预测网站结合小鼠胚胎着床芯片数据预测了mir-21的5个与着床相关的靶基因:Reck、F3、Upk1 b、Ggh、Tmed6,通过分别构建含有靶基因3′UTR的重组报告载体、pre-mir-21或/和mir-21inhibitor体外转染细胞、双荧光素酶活性分析初步确定mir-21的靶位点。pre-mir-21可显著降低转染上述5个重组载体的细胞内荧光素酶活性;mir-21 inhibitor可显著增加转染Reck、Upk1 b和Tmed63′UTR的重组载体的细胞内荧光素酶活性;pre-mir-21和mir-21 inhibitor共转染可分别显著增加转染含有Reck3′UTR、F33′UTR、Upk1 b3′UTR和Ggh3′UTR的重组载体的细胞内荧光素酶活性。Reck和Upk1b可能是mir-21的靶基因。To dissect the molecular basis underlying mir-21 associated embryo implantation, putative mir-21 targets (Reck, F3, Ggh and Tmed6)that are likely involved in mouse embryo implantation were examined by the establishment of in vitro transfection cells and dual-luciferase activity assay. These transfection cells contain a recombinant reporter with 3′UTR of the targets downstream of luciferase gene, and pre-mir-21 and/or mir-21 inhibitor. The results showed that pre-mir-21 can significantly decrease the luciferase activity in all the cells transfected with the reporter, whereas mir-21 inhibitor can only significantly increase the fluorescence activity in Reck, Upk1b and Tmed6. Pre-mir-21 and mir-21 inhibitor cotransfection can significantly decrease the fluorescence activity in Reck, F3, Upklb and Ggh. In conclusion, Reck and Upklb might be the targets of mir-21.
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