Tian Hong, Chen Yan, Wu Jinyan, Lin Tong, Liu Xiangtao
Key Laboratory of Animal Virology of Ministry of Agriculture/State Key Laboratory of Veterinary Etiological Biology/Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, China.
Key Laboratory of Animal Virology of Ministry of Agriculture/State Key Laboratory of Veterinary Etiological Biology/Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, China.
Res Vet Sci. 2016 Oct;108:93-7. doi: 10.1016/j.rvsc.2016.08.005. Epub 2016 Aug 24.
Orf virus (ORFV) causes contagious ecthyma, a non-systemic skin disease in sheep and goat. Bioinformatics analysis showed that ORFV125 has Bcl-2-like homologous domain and 3D structurally, it is generally known that Bcl-2 protein is known to be a key protein to control cell apoptosis. Maybe ORFV125 act as a Bcl-2-like manner to control cell apoptosis, but its exact function isn't very clear. So in this study, we use yeast two-hybrid system to identity the putative host cell protein interacting partners of ORFV125, and meanwhile using the data obtained from the Gene Ontology, Uniprot, and Kyoto Encyclopedia of Genes and Genomes databases to analysis the functions and pathways associated with them. Finally, five host proteins were shown to be interacted with ORFV125, including cytochrome b (cytb) gene, GUCY2C, BIRC5, GTF3C6 and SERBP1, we also found that BIRC5 has complex biological functions, can inhibit apoptosis, promote cell transformation and are involved in mitosis, and the interaction network of BIRC5 and ORFV125 were constructed. These findings provide a foundation to better understand the biology of the interactions between ORFV125 and the host proteins with which it directly interacts with and resultant downstream events.
羊口疮病毒(ORFV)可引发传染性脓疱性皮炎,这是一种发生于绵羊和山羊的非系统性皮肤疾病。生物信息学分析表明,ORFV125具有Bcl-2样同源结构域,从三维结构来看,众所周知Bcl-2蛋白是控制细胞凋亡的关键蛋白。或许ORFV125以类似Bcl-2的方式发挥作用来控制细胞凋亡,但其确切功能尚不清楚。因此,在本研究中,我们利用酵母双杂交系统来鉴定与ORFV125相互作用假定的宿主细胞蛋白伙伴,同时利用从基因本体论、通用蛋白质数据库和京都基因与基因组百科全书数据库获得的数据来分析与之相关的功能和途径。最终,显示有5种宿主蛋白与ORFV125相互作用,包括细胞色素b(cytb)基因、GUCY2C、BIRC5、GTF3C6和SERBP1,我们还发现BIRC5具有复杂的生物学功能,可抑制细胞凋亡、促进细胞转化并参与有丝分裂,且构建了BIRC5与ORFV125的相互作用网络。这些发现为更好地理解ORFV125与其直接相互作用的宿主蛋白之间相互作用的生物学特性以及由此产生的下游事件奠定了基础。