WANG Ye-Fu, JI Xi-Peng, ZHU Ying, LI Xiao-Feng and LI Zhi-Da. An antiapoptosis p35 gene from Heliothis armigera polyhedrosis virus rescues Acp352 replication in non-permissible cell line[J]. Virologica Sinica, 1998, 13(3).
Citation: WANG Ye-Fu, JI Xi-Peng, ZHU Ying, LI Xiao-Feng, LI Zhi-Da. An antiapoptosis p35 gene from Heliothis armigera polyhedrosis virus rescues Acp352 replication in non-permissible cell line .VIROLOGICA SINICA, 1998, 13(3) : 256.

棉铃虫核型多角体病毒凋亡抑制基因对p35基因失活病毒的功能拯救

  • 野生型苜蓿银纹夜蛾核型多角体病毒(AcNPV)能感染棉铃虫细胞,不引起细胞凋亡,用LacZ基因使AcNPV凋亡抑制基因p35插入失活,得到缺陷病毒Acp35Z能迅速引起棉铃虫细胞凋亡,但缺陷病毒本身不能复制。用AcNPV即早期基因IE1启动子带动棉铃虫杆状病毒(HaNPV)p35基因在棉铃虫细胞中瞬时表达,能拯救p35基因失活病毒Acp35Z复制。通过X-gal显色反应和dotELISA分别检测到了半乳糖苷酶的活性和p35基因的表达,证明了所克隆的HaNPVp35基因不仅是一个凋亡抑制基因,也是一个与杆状病毒复制相关的基因,它的瞬时表达能支持Acp35Z在棉铃虫细胞中复制。

An antiapoptosis p35 gene from Heliothis armigera polyhedrosis virus rescues Acp352 replication in non-permissible cell line

  • p35 gene from baculovirus is an antiapoptosis gene which can sustain virus multiplication when infected by baculovirus. Both p35 deleted and inserting inactivated AcNPV can not replicate in Sf cell lines and Ha cell line.It is almost the same in BmNPV.Acp35Z which generated from AcNPV inserted LacZ gene whthin p35 gene causes apoptosis in Ha cell line ,but the abortion replication can be rescued by transient expression of HaNPV p35 gene drived by AcNPV IE1 promotor.The result was reconfirmed with X-gal manifest and Dot-ELISA.

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    An antiapoptosis p35 gene from Heliothis armigera polyhedrosis virus rescues Acp352 replication in non-permissible cell line

    • 1. Institute of Virology.Wuhan University,Wuhan 430072

    Abstract: p35 gene from baculovirus is an antiapoptosis gene which can sustain virus multiplication when infected by baculovirus. Both p35 deleted and inserting inactivated AcNPV can not replicate in Sf cell lines and Ha cell line.It is almost the same in BmNPV.Acp35Z which generated from AcNPV inserted LacZ gene whthin p35 gene causes apoptosis in Ha cell line ,but the abortion replication can be rescued by transient expression of HaNPV p35 gene drived by AcNPV IE1 promotor.The result was reconfirmed with X-gal manifest and Dot-ELISA.

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