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Identification of Pns12 as the second silencing suppressor of Rice gall dwarf virus 被引量:7
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作者 WU JianGuo WANG ChunZheng +5 位作者 du zhengguo CAI LiJun HU MeiQun WU ZuJian LI Yi XIE LianHui 《Science China(Life Sciences)》 SCIE CAS 2011年第3期201-208,共8页
RNA silencing is a conserved mechanism found ubiquitously in eukaryotic organisms.It has been used to regulate gene expression and development.In addition,RNA silencing serves as an important mechanism in plants' ... RNA silencing is a conserved mechanism found ubiquitously in eukaryotic organisms.It has been used to regulate gene expression and development.In addition,RNA silencing serves as an important mechanism in plants' defense against invasive nucleic acids,such as viruses,transposons,and transgenes.As a counter-defense,most plants,and some animal viruses,encode RNA silencing suppressors to interfere at one or several points of the silencing pathway.In this study,we showed that Pns12 of RGDV (Rice gall dwarf virus) exhibits silencing suppressor activity on the reporter green fluorescent protein in transgenic Nicotiana benthamiana line 16c.Pns12 of RGDV suppressed local silencing induced by sense RNA but had no effect on that induced by dsRNA.Expression of Pns12 also enhanced Potato virus X pathogenicity in N.benthamiana.Collectively,these results suggested that RGDV Pns12 functions as a virus suppressor of RNA silencing,which might target an upstream step of dsRNA formation in the RNA silencing pathway.Furthermore,we showed that Pns12 is localized mainly in the nucleus of N.benthamiana leaf cells. 展开更多
关键词 水稻瘤矮病毒 RNA沉默 双链RNA 鉴定 绿色荧光蛋白 马铃薯X病毒 真核生物 基因表达
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口蹄疫病毒3B蛋白的表达纯化及其多克隆抗体的制备
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作者 辛旭 吴香菊 +5 位作者 齐静 王永志 李相安 杜正国 单虎 杜以军 《畜牧与兽医》 北大核心 2021年第3期109-114,共6页
为了深入研究口蹄疫病毒3B蛋白的结构及功能,本研究原核表达了3B蛋白并制备了针对3B蛋白的多克隆抗体。试验采用PCR方法扩增了口蹄疫病毒3B蛋白基因,并将其克隆到pET28a载体上,构建了重组质粒pET28a-3B,将其转化到大肠杆菌BL21感受态细... 为了深入研究口蹄疫病毒3B蛋白的结构及功能,本研究原核表达了3B蛋白并制备了针对3B蛋白的多克隆抗体。试验采用PCR方法扩增了口蹄疫病毒3B蛋白基因,并将其克隆到pET28a载体上,构建了重组质粒pET28a-3B,将其转化到大肠杆菌BL21感受态细胞中进行诱导表达。经过Ni-NTA琼脂糖亲和层析法初步纯化及Millipore超滤浓缩进一步纯化,将其免疫试验动物新西兰大白兔后制备出了抗3B蛋白的多克隆抗体。通过ELISA检测了该多抗的效价,Western blot试验检测了其反应性,通过间接免疫荧光(IFA)和Western blot试验检测了该多抗的应用性。结果表明:该抗体的效价为1∶512000,反应性良好;IFA试验和Western blot试验中可以检测到过表达后定位于细胞核和细胞质中的3B蛋白,也可以检测到在真核细胞中过表达的3B蛋白。说明本研究制备的口蹄疫病毒3B蛋白多克隆抗体可以作为开展该病毒相关研究的重要材料。 展开更多
关键词 口蹄疫病毒 3B蛋白 原核表达 蛋白纯化 多克隆抗体
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