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一种粉纹夜蛾颗粒体病毒的杆状病毒抗凋亡基因同源物。

A baculovirus anti-apoptosis gene homolog of the Trichoplusia ni granulovirus.

作者信息

Bideshi D K, Anwar A T, Federici B A

机构信息

Graduate Program in Genetics, Department of Entomology University of California, Riverside Riverside, California 92521, USA.

出版信息

Virus Genes. 1999;19(2):95-101. doi: 10.1023/a:1008148922330.

Abstract

An inhibitor of apoptosis (iap) gene homolog (Tn-iap) of the Trichoplusia ni granulovirus (TnGV) was cloned, sequenced and mapped on the genome of TnGV. Tn-iap encoded a protein (Tn-IAP) of 301 amino acids with a predicted molecular mass of 35 kDa. The Tn-IAP contained the two sequence motifs, BIRs and RING finger, characteristic of IAP proteins, and shared identities of 21-27% and similarities of 28-53% with IAP proteins of Cydia pomonella GV (Cp-IAP), Orgyia pseudotsugata multinucleocapsid nucleopolyhedrovirus (MNPV) (Op-IAP1, 3), Autographa californica MNPV (Ac-IAP1), Bombyx mori NPV (Bm-IAP1), Lymantria dispar MNPV (Ld-IAP3) and Buzura suppressaria single nucleocapsid NPV (Bs-IAP1). However, Tn-IAP shared no significant homology with baculovirus IAP2 proteins. Using an antisense Tn-iap probe, two major transcripts of approximately 800 nt and 1600 nt were detected by Northern blot analysis of RNA extracted from the fat body of T. ni larvae infected with the TnGV. Unlike Cp-IAP and Op-IAP3, however, Tn-IAP did not rescue virion occlusion in SF21 cells infected with a p35-deficient AcMNPV mutant. Tn-IAP's synthesis in vivo but failure to rescue p35-deficient AcMNPV in SF21 cells suggests it is a functional IAP that is only effective in certain cell types.

摘要

克隆、测序了粉纹夜蛾颗粒体病毒(TnGV)的凋亡抑制因子(iap)基因同源物(Tn-iap),并将其定位到TnGV基因组上。Tn-iap编码一个由301个氨基酸组成的蛋白质(Tn-IAP),预测分子量为35 kDa。Tn-IAP含有IAP蛋白特有的两个序列基序,即杆状病毒IAP重复序列(BIRs)和指环结构域,与苹果蠹蛾颗粒体病毒(Cp-IAP)、云杉芽卷叶蛾多核衣壳核多角体病毒(MNPV)(Op-IAP1、3)、苜蓿银纹夜蛾多核衣壳核多角体病毒(Ac-IAP1)、家蚕核型多角体病毒(Bm-IAP1)、舞毒蛾多核衣壳核多角体病毒(Ld-IAP3)和桑毛虫单核衣壳核多角体病毒(Bs-IAP1)的IAP蛋白具有21%-27%的同一性和28%-53%的相似性。然而,Tn-IAP与杆状病毒IAP2蛋白没有显著同源性。使用反义Tn-iap探针,通过对感染TnGV的粉纹夜蛾幼虫脂肪体提取的RNA进行Northern印迹分析,检测到约800 nt和1600 nt的两个主要转录本。然而,与Cp-IAP和Op-IAP3不同,Tn-IAP不能拯救感染p35缺陷型AcMNPV突变体的SF21细胞中的病毒粒子包埋。Tn-IAP在体内的合成,但未能在SF21细胞中拯救p35缺陷型AcMNPV,表明它是一种仅在某些细胞类型中有效的功能性IAP。

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