Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia; The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
J Invest Dermatol. 2018 Dec;138(12):2558-2567. doi: 10.1016/j.jid.2018.06.169. Epub 2018 Jun 30.
Persistent human papillomavirus (HPV) infection is responsible for at least 5% of human malignancies. Most HPV-associated cancers are initiated by the HPV16 genotype, as confirmed by detection of integrated HPV DNA in cells of oral and anogenital epithelial cancers. However, single-cell RNA sequencing may enable prediction of HPV involvement in carcinogenesis at other sites. We conducted single-cell RNA sequencing on keratinocytes from a mouse transgenic for the E7 gene of HPV16 and showed sensitive and specific detection of HPV16-E7 mRNA, predominantly in basal keratinocytes. We showed that increased E7 mRNA copy number per cell was associated with increased expression of E7 induced genes. This technique enhances detection of active viral transcription in solid tissue and may clarify possible linkage of HPV infection to development of squamous cell carcinoma.
持续性人乳头瘤病毒(HPV)感染是导致至少 5%的人类恶性肿瘤的原因。大多数 HPV 相关癌症是由 HPV16 基因型引起的,这一点已通过在口腔和肛门生殖器上皮癌的细胞中检测到整合的 HPV DNA 得到证实。然而,单细胞 RNA 测序可能能够预测 HPV 在其他部位致癌作用。我们对 HPV16 的 E7 基因转基因小鼠的角蛋白细胞进行了单细胞 RNA 测序,结果表明,能够敏感和特异地检测 HPV16-E7 mRNA,主要在基底角蛋白细胞中。我们表明,每个细胞中 E7 mRNA 拷贝数的增加与 E7 诱导基因的表达增加有关。该技术增强了对实体组织中活跃病毒转录的检测,并可能阐明 HPV 感染与鳞状细胞癌发展之间的可能联系。