Wurdak M, Schneider M, Iftner T, Stubenrauch F
Division of Experimental Virology, University Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
J Gen Virol. 2018 Mar;99(3):344-354. doi: 10.1099/jgv.0.001012.
SP100 proteins are components of nuclear domain 10 structures and have been implicated as inhibitors of human papillomavirus (HPV) replication. In this study, we have addressed the role of SP100 in tumour formation by the cottontail rabbit () papillomavirus (CRPV or SfPV1) in a rabbit model. Tissue culture studies using rabbit keratinocyte lines indicated that rabbit SP100 is an interferon-beta-inducible gene similar to its human counterpart. Stable knockdown of SP100 by shRNA in a cell line harbouring CRPV genomes resulted in a decrease of viral early transcripts. In contrast, infection of domestic rabbits with recombinant CRPV genomes expressing short hairpin (sh)RNAs directed against SP100 did not reveal changes in tumour formation rate, tumour size or early viral transcript levels. However, late viral transcript levels and viral genome copies were consistently lower in CRPV/shSP100-induced tumours than in the control, but these differences did not reach statistical significance. In summary, this study suggests that rabbit SP100 is not an inhibitor but an activator of CRPV replication and transcription.
SP100蛋白是核结构域10的组成成分,并且被认为是人类乳头瘤病毒(HPV)复制的抑制剂。在本研究中,我们通过兔模型探讨了SP100在棉尾兔乳头瘤病毒(CRPV或SfPV1)致瘤过程中的作用。使用兔角质形成细胞系进行的组织培养研究表明,兔SP100是一种类似于其人类对应物的β-干扰素诱导基因。在携带CRPV基因组的细胞系中,通过shRNA稳定敲低SP100导致病毒早期转录本减少。相比之下,用表达针对SP100的短发夹(sh)RNA的重组CRPV基因组感染家兔,未发现肿瘤形成率、肿瘤大小或病毒早期转录本水平有变化。然而,CRPV/shSP100诱导的肿瘤中病毒晚期转录本水平和病毒基因组拷贝数始终低于对照组,但这些差异未达到统计学显著性。总之,本研究表明兔SP100不是CRPV复制的抑制剂,而是激活剂。