McArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Departments of Chemistry and Biomolecular Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
mBio. 2023 Dec 19;14(6):e0245823. doi: 10.1128/mbio.02458-23. Epub 2023 Oct 31.
The Mus musculus papillomavirus 1 (MmuPV1) E6 and E7 proteins are required for MmuPV1-induced disease. Our understanding of the activities of MmuPV1 E6 has been based on affinity purification/mass spectrometry studies where cellular interacting partners of MmuPV1 E6 were identified, and these studies revealed that MmuPV1 E6 can inhibit keratinocyte differentiation through multiple mechanisms. We report that MmuPV1 E6 encodes additional activities including the induction of proliferation, resistance to density-mediated growth arrest, and decreased dependence on exogenous growth factors. Proteomic and transcriptomic analyses provided evidence that MmuPV1 E6 increases the expression and steady state levels of a number of cellular proteins that promote cellular proliferation and other hallmarks of cancer. These results indicate that MmuPV1 E6 is a major driver of MmuPV1-induced pathogenesis.
小鼠乳头瘤病毒 1(MmuPV1)的 E6 和 E7 蛋白是导致 MmuPV1 诱导疾病所必需的。我们对 MmuPV1 E6 活性的理解是基于亲和纯化/质谱研究,其中鉴定了 MmuPV1 E6 的细胞相互作用伙伴,这些研究表明 MmuPV1 E6 可以通过多种机制抑制角质形成细胞分化。我们报告说,MmuPV1 E6 还具有其他活性,包括诱导增殖、抵抗密度介导的生长抑制以及减少对外源生长因子的依赖。蛋白质组学和转录组学分析提供了证据,表明 MmuPV1 E6 增加了许多促进细胞增殖和癌症其他特征的细胞蛋白的表达和稳定水平。这些结果表明,MmuPV1 E6 是 MmuPV1 诱导发病机制的主要驱动因素。