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作 者:苟德明[1] 郑新民[1] 陈乃清[1] 魏庆信 樊俊华 赵浩斌[1] 龙文 路兴中[1]
机构地区:[1]西北农业大学动物科学系
出 处:《中国兽医学报》1996年第6期570-575,共6页Chinese Journal of Veterinary Science
基 金:国家"863"资助项目;湖北省自然科学基金
摘 要:以绵羊金属硫蛋白基因(oMT)为启动子,构建了2种结构的HSA质粒:poMTHSA和poMTHSAUD。其中poMTHSA是将HSAcDNA直接置于oMT启动子的控制下,以pSPORT1为载体构建而成;而poMTHSAUD另融有HSA基因5′,3′侧翼序列(包括内含子1,2,13,14)。将这2种结构的质粒用NotⅠ线化后,注入昆明种小鼠受精卵的雄原核,再移植到假孕受体鼠的输卵管。共注射577枚受精卵,有406枚形态完好的注射卵被移植到19只假孕受体,其中8只妊娠,产仔35只。经PCR及Southern杂交检测,获得了4只转基因小鼠,其中1只来自于注射poMTHSA,3只来自于注射poMTHSAUD。转基因总阳性率和总效率分别为11.4%和0.7%。用RT-PCR技术在转录水平检测4只转基因鼠外源基因的表达情况,结果2只鼠(均来自于注射poMTHSAUD)在肝脏中表达有HSAmRNA,免疫琼脂试验发现,这2只小鼠的血液中均有HSA的表达产物,与RT-PCR检测结果一致。poMTHSAUD在小鼠体内得到了整合和表达;而poMTHSA只有整合而未得到表达,故认为含有侧翼序列及部分内含子的基因poMTHSAUD优?Using ovine metallothionein (oMT) as promoter, two structural HSA fused genes (poMTHSA and poMTHSAUD) were constructed. poMTHSA consists of oMT promoter and HSA cDNA. poMTHSAUD fused 5′,3′ flanking sequences (included intron 1, 2, 13, 14) additionally compared with poMTHSA. The two recombinant genes in linear form (Not Ⅰ cut), were microinjected into the male pronuclei of fertillized egg through Leitz microinjector. During this study, 577 fertillized eggs from donor mice were injected, and 406 normal eggs injected were transferred to the oviduct of 19 pseudopregnant recipient mice, 8 of 19 recipient mice became gestation and gave birth to 35 F 1 offspring mice. The zygote′s survival rate and birth rate were 70.4% and 8.6%, respectively. 4 of 35 mice integerated the foreign HSA gene detected by PCR and Southern hybridization, one from poMTHSA, the others from poMTHSAUD. Total integration rates and efficiency of transgene were 11.4% and 0.7%, respectively. Transgene expression was analyzed to the transcriptional level by RT PCR. The results showed that 2 transgenic mice expressed HSA mRNA in their livers. To detect the expression products of HSA, serum samples from 4 transgenic mice were analyzed by immunoassay of agarose expansion experiment. It was proved that 2 transgenic mice expressed HSA. There was a complete correlation between immunoassay and RT PCR. The results demonstrated that the foreign poMTHSAUD gene was expressed in the body of transgenic mice, but poMTHSA gene was integrated only. It is suggested that the poMTHSAUD fused 5′, 3′ flanking sequences and some introns seems to be more suitable to transgene than the poMTHSA.
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