CAJ | 학술논문

为筛选山羊痘病毒(GTPV)的外源基因插入区,本研究以GTPV Pellor株为模板,设计2对引物,PCR扩增AV 41株GTPV_gp024基因相邻上下游长度约1.1 kb的同源重组片段,分别插入质粒pGPT-EGFP中.插入部位在痘病毒双向启动子p11～p7.5启动的报告基因EGFP-GPT上下游,构建转移载体pEG024,并转染已感染GTPV Av 41病毒的LT细胞,经GPT加压筛选7代后得到重组病毒.结果显示,重组病毒稳定表达报告基因EGFP,从而表明GTPV_gp024基因能够作为外源基因的插入区.
위사선산양두병독(GTPV)적외원기인삽입구,본연구이GTPV Pellor주위모판,설계2대인물,PCR확증AV 41주GTPV_gp024기인상린상하유장도약1.1 kb적동원중조편단,분별삽입질립pGPT-EGFP중.삽입부위재두병독쌍향계동자p11～p7.5계동적보고기인EGFP-GPT상하유,구건전이재체pEG024,병전염이감염GTPV Av 41병독적LT세포,경GPT가압사선7대후득도중조병독.결과현시,중조병독은정표체보고기인EGFP,종이표명GTPV_gp024기인능구작위외원기인적삽입구.
In this study, two circumferential fragments covering 1.1 kb approximately of the locus of "GTPV_gp024" were amplified by PCR with specific primers based on GTPV strain Pellor. The PCR fragments were cloned into upstream and downstream of the enhanced green fluorescent protein (EGFP) of pGPT-EGFP vector modulated by bi-directional promoter pl 1-p7.5 originated from fowlpox virus. The recombinant transfer vector was co-transinfected into GTPV strain AV 41 infected LT cells. A recombinant GTPV strain was obtained after 7 rounds screening under GPT pressure. The results showed that EGFP was expressed stably by the recombinant GTPV, and the GTPV_gp024 locus could be used as a novel region for expression of foreign genes.