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Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.

ABSTRACT: HPV16 causes half of cervical cancers worldwide; for unknown reasons, most infections resolve within two years. Here, we analyze the viral genomes of 5,328 HPV16-positive case-control samples to investigate mutational signatures and the role of human APOBEC3-induced mutations in viral clearance and cervical carcinogenesis. We identify four de novo mutational signatures, one of which matches the COSMIC APOBEC-associated signature 2. The viral genomes of the precancer/cancer cases are less likely to contain within-host somatic HPV16 APOBEC3-induced mutations (Fisher's exact test, P = 6.2 x 10^-14), and have a 30% lower nonsynonymous APOBEC3 mutation burden compared to controls. We replicate the low prevalence of HPV16 APOBEC3-induced mutations in 1,749 additional cases. APOBEC3 mutations also historically contribute to the evolution of HPV16 lineages. We demonstrate that cervical infections with a greater burden of somatic HPV16 APOBEC3-induced mutations are more likely to be benign or subsequently clear, suggesting they may reduce persistence, and thus progression, within the host.

SUBMITTER: Zhu B

PROVIDER: S-EPMC7021686 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.

Zhu Bin B Xiao Yanzi Y Yeager Meredith M Clifford Gary G Wentzensen Nicolas N Cullen Michael M Boland Joseph F JF Bass Sara S Steinberg Mia K MK Raine-Bennett Tina T Lee DongHyuk D Burk Robert D RD Pinheiro Maisa M Song Lei L Dean Michael M Nelson Chase W CW Burdett Laurie L Yu Kai K Roberson David D Lorey Thomas T Franceschi Silvia S Castle Philip E PE Walker Joan J Zuna Rosemary R Schiffman Mark M Mirabello Lisa L

Nature communications 20200214 1

HPV16 causes half of cervical cancers worldwide; for unknown reasons, most infections resolve within two years. Here, we analyze the viral genomes of 5,328 HPV16-positive case-control samples to investigate mutational signatures and the role of human APOBEC3-induced mutations in viral clearance and cervical carcinogenesis. We identify four de novo mutational signatures, one of which matches the COSMIC APOBEC-associated signature 2. The viral genomes of the precancer/cancer cases are less likely ...[more]

PMID: 32060290

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Project description:APOBEC3 proteins (A3s) play an important role in host innate immunity against viruses and DNA mutations in cancer. A3s-induced mutations in both viral and human DNA genomes vary significantly from non-lethal mutations in viruses to localized hypermutations, such as kataegis in cancer. How A3s are regulated remains largely unknown. Since A3s exist in complexes and belong to the same family as APOBEC-1 (A1), which requires cofactors to be functional, we investigated the role of A1 cofactors and other A3 potentially associated hnRNPs on A3 mutational activity using hepatitis B virus (HBV) cellular replication as a model. We found that A1-associated cofactors and other hnRNPs were involved in A3 mutational activity regulation, and their regulatory effect was dependent on the strength of A3 association with hnRNPs with an order of A3C > 3G>3B and A1 cofactors > other hnRNPs. A1 cofactors had a strong protein interaction with A3 and significantly increased A3 mutational activity by co-expression. Endogenous gene expression knockdown by siRNA had the opposite decrease effect. Disruption of the protein interactions between A3 and hnRNPs through A3G and A3B mutagenesis decreased A3 mutational activity significantly, even to a level of near total loss, indicating that A1 cofactors and hnRNPs are required for A3 mutational activity. HBV genome-wide mutation analyses showed that A1 cofactors significantly increased A3C accessibility to HBV (-)DNA and A3C-induced mutational efficiency to generate kataegis-like hypermutation. These data demonstrate that A1 cofactors and hnRNPs are closely associated with A3s and may play an important regulatory role under physiological conditions.ImportanceAs human host restriction factors, A3s play an important role against viral infections. A3s are also major mutagenic drivers of cancer. However, why A3-induced mutations vary significantly from non-lethal mutations in virus to localized hypermutations in cancer remains unknown. We found that A1 cofactor and other hnRNPs are not only associated with A3 complexes but also play important regulatory roles in A3-induced mutation activities. A1 cofactors like GRY-RBP significantly increased A3 accessibility and mutational efficiency to its single-strand DNA substrate during HBV reverse transcription to generate hypermutations. Disruption of the A3 protein association with hnRNPs by A3 mutagenesis diminished A3 mutational activity. This finding not only reveals a regulatory mechanism for A3-induced mutation but also indicates that A3-associated cellular factors can be a potential target for regulating A3-induced mutation for cancer therapeutics.

Dataset Information

Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.

Publications

Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.

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