Kang D, Lundström A, Steiner H
Department of Microbiology, Stockholm University, Sweden.
Gene. 1996 Oct 3;174(2):245-9. doi: 10.1016/0378-1119(96)00089-3.
The mRNA differential display method was used to isolate antibacterial defense genes from Trichoplusia ni. The mRNA population in last-instar T. ni larvae injected with bacteria was compared to that of untreated larvae. Using a PCR amplified probe corresponding to an induced mRNA, we were able to clone an attacin homolog from a lambda cDNA library from vaccinated larvae. The corresponding protein showed 63% identity to Hyalophora cecropia acidic attacin. The induction kinetics of T. ni attacin A gave optimal mRNA levels at 20 h post-infection. Genomic analysis showed this to be a single-copy gene with two introns.
采用mRNA差异显示法从粉纹夜蛾中分离抗菌防御基因。将注射细菌的末龄粉纹夜蛾幼虫的mRNA群体与未处理幼虫的mRNA群体进行比较。使用与诱导mRNA对应的PCR扩增探针,我们能够从接种疫苗幼虫的λ cDNA文库中克隆出一种attacin同源物。相应的蛋白质与天蚕酸性attacin的同一性为63%。粉纹夜蛾attacin A的诱导动力学在感染后20小时达到最佳mRNA水平。基因组分析表明这是一个具有两个内含子的单拷贝基因。