生物
基因型
人乳头瘤病毒
病毒学
序列(生物学)
序列分析
遗传学
计算生物学
生物信息学
肿瘤科
基因
内科学
医学
作者
R.N. Jones,Sayuri Miyauchi,Roy S,Nathalie Boutros,Jyoti Mayadev,Loren K. Mell,Joseph A. Califano,Aldo Venuti,Andrew B. Sharabi
出处
期刊:Virology
[Elsevier]
日期:2024-02-01
卷期号:590: 109946-109946
标识
DOI:10.1016/j.virol.2023.109946
摘要
There are over 220 identified genotypes of Human papillomavirus (HPV), and the HPV genome encodes 3 major oncogenes, E5, E6, and E7. Conservation and divergence in protein sequence and function between low-risk versus high-risk oncogenic HPV genotypes has not been fully characterized. Here, we used modern computational and structural folding algorithms to perform a comparative analysis of HPV E5, E6, and E7 between multiple low risk and high risk genotypes. We first identified significantly greater sequence divergence in E5 between low- and high-risk genotypes compared to E6 and E7. Next we used, AlphaFold to model the structure of papillomavirus proteins and complexes with high confidence, including some with no established consensus structure. We observed that HPV E5, but not E6 or E7, had a dramatically different 3D structure between low-risk and high-risk genotypes. To our knowledge, this is the first comparative analysis of HPV proteins using the artificial-intelligence driven Alphafold platform. The marked differences in E5 sequence and structure in high-risk HPVs may contribute in important and underappreciated ways to the development of HPV-associated cancers.
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