Suppr超能文献

家蚕核型多角体病毒凋亡抑制基因功能分析。

Functional analysis of the inhibitor of apoptosis genes in Antheraea pernyi nucleopolyhedrovirus.

机构信息

Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Hubei, Wuhan, 430030, PR China.

出版信息

J Microbiol. 2010 Apr;48(2):199-205. doi: 10.1007/s12275-010-9108-y. Epub 2010 May 1.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验