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A novel short transcript isoform of chicken IRF7 negatively regulates interferon-βproduction
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作者 MA Yu-chen CHEN Hua-yuan +5 位作者 GAO Shen-yan ZHANG Xiao-zhan LI Yong-tao YANG Xia ZHAO Jun WANG Zeng 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2023年第7期2213-2220,共8页
Type I interferon(IFN-I)provides an important first line to protect avian species against pathogens invasion.IFN regulatory factor 7(IRF7)has been identified as the most important regulator for both DNA and RNA virus-... Type I interferon(IFN-I)provides an important first line to protect avian species against pathogens invasion.IFN regulatory factor 7(IRF7)has been identified as the most important regulator for both DNA and RNA virus-induced IFN-I production in chickens.Although four splicing variants of IRF7 have been identified in mammals,it is still unclear whether alternative splicing patterns and the function of IRF7 isoform(s)exist in chickens.In this study,we reported a novel short transcript isoform of chicken IRF7(chIRF7),termed chIRF7-iso,which contained an intact N-terminal DNA-binding domain(DBD)and 14 amino acids different from chIRF7 in the C-terminal.Overexpression of chIRF7 in chicken leghorn male hepatocellular(LMH)cells activated the IFN-βpromoter and significantly inhibited Newcastle disease virus(NDV)and fowl adenovirus serotype 4(FAdV-4)replication.Conversely,overexpression of chIRF7-iso blocked the IFN-βpromoter activity and was favorable for NDV and FAdV-4 replication in vitro.Collectively,our results confirm that a novel chIRF7 isoform-mediated negative regulates IFN-βproduction,which will contribute to understanding the role of chIRF7 in innate antiviral response in chicken. 展开更多
关键词 chirf7 chirf7 isoform negative regulation IFN-Β
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鸡干扰素调节因子7的原核表达及多克隆抗体的制备 被引量:3
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作者 崔鹏飞 邓国华 +2 位作者 韦良孟 焦培荣 廖明 《动物医学进展》 CSCD 北大核心 2013年第4期1-4,共4页
为表达鸡干扰素调节因子7蛋白并制备其多克隆抗体,通过RT-PCR技术扩增chIRF7基因的编码序列,构建重组质粒PET30a-chIRF7。将重组质粒转化至大肠埃希菌(E.coil)BL21(DE3)后经IPTG诱导,SDS-PAGE结果显示,重组蛋白rchIRF7分子量约为60ku。... 为表达鸡干扰素调节因子7蛋白并制备其多克隆抗体,通过RT-PCR技术扩增chIRF7基因的编码序列,构建重组质粒PET30a-chIRF7。将重组质粒转化至大肠埃希菌(E.coil)BL21(DE3)后经IPTG诱导,SDS-PAGE结果显示,重组蛋白rchIRF7分子量约为60ku。将纯化的重组蛋白免疫接种小鼠制备多克隆抗体,间接ELISA测定血清抗体滴度在1∶51 200以上,IFA检测结果显示制备的鼠抗chIRF7蛋白多抗能够与AIV刺激的CEF细胞内的chIRF7蛋白发生特异性反应,表明通过原核表达系统表达的重组蛋白rchIRF7具有很好的免疫原性,以其制备的鼠抗chIRF7蛋白多克隆抗体滴度高、特异性好。 展开更多
关键词 鸡干扰素调节因子7 原核表达 多克隆抗体
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