Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Hubei, Wuhan, 430030, PR China.
J Microbiol. 2010 Apr;48(2):199-205. doi: 10.1007/s12275-010-9108-y. Epub 2010 May 1.
The inhibitor of apoptosis proteins (IAP) plays an important role in cell apoptosis. We cloned two novel IAP family members, Ap-iap1 and Ap-iap2, from Antheraea pernyi nucleopolyhedrovirus (ApNPV) genome. Ap-IAP1 contains two baculoviral IAP repeat (BIR) domains followed by a RING domain, but Ap-IAP2 has only one BIR domain and RING. The result of transient expression in Spodoptera frugiperda (Sf21) showed that Ap-iap1 blocked cell apoptosis induced by actinomycin D treatment and also rescued the p35 deficient Autographa californica nucleopolyhedrovirus (AcNPV) to replicate in Sf9 cells, while Ap-iap2 does not have this function. Several Ap-IAP1 truncations were constructed to test the activity of BIRs or RING motif to inhibit cell apoptosis. The results indicated that BIRs or RING of Ap-IAP1 had equally function to inhibit cell apoptosis. Therefore deletion of above both of the above domains could not block apoptosis induced by actinomycin D or rescue the replication of AcMNPV Delta p35. We also screened two phage-display peptides that might interact with Ap-IAP1.
凋亡抑制蛋白(IAP)在细胞凋亡中起着重要作用。我们从野蚕核型多角体病毒(ApNPV)基因组中克隆了两个新的 IAP 家族成员 Ap-iap1 和 Ap-iap2。Ap-IAP1 包含两个杆状病毒 IAP 重复(BIR)结构域,后面跟着一个 RING 结构域,但 Ap-iap2 只有一个 BIR 结构域和 RING。在 Spodoptera frugiperda(Sf21)中的瞬时表达结果表明,Ap-iap1 阻断了放线菌素 D 处理诱导的细胞凋亡,并且还挽救了缺乏 p35 的 Autographa californica 核型多角体病毒(AcNPV)在 Sf9 细胞中的复制,而 Ap-iap2 没有此功能。构建了几种 Ap-IAP1 截断体来测试 BIR 或 RING 基序抑制细胞凋亡的活性。结果表明,Ap-IAP1 的 BIR 或 RING 具有同等的抑制细胞凋亡的功能。因此,上述两个结构域的缺失不能阻断放线菌素 D 诱导的凋亡或挽救 AcMNPV Delta p35 的复制。我们还筛选了两个可能与 Ap-IAP1 相互作用的噬菌体展示肽。