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Hill Lab, University of York

Molecular mechanisms of viral gene expression

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Viruses do things differently

RNA viruses rely on highly structured RNA molecules to control every stage of their replication cycles. Far from acting simply as carriers of genetic information, viral RNAs adopt complex three-dimensional folds that interact with ribosomes, viral enzymes and host proteins to regulate protein synthesis, genome replication and the assembly of new virus particles. Understanding how these dynamic RNA-protein complexes function is central to explaining how viruses replicate, evolve and cause disease.

We're trying to better understand these events at a molecular level.

Latest Publications

The cardioviruses (e.g. EMCV, TMEV) exhibit the highest known viral PRF efficiency in nature, with up to 85% of ribosomes changing frame. This is an unusual case: the viral 2A protein is required to activate frameshifting through an unknown mechanism. Here, we combine single-molecule FRET and SAXS to show how 2A binding induces a striking conformational change in the RNA stimulatory element, switching it from a stem-loop into a pseudoknot. A 1.9 Å X-ray crystal structure of the complex reveals the mechanism by which 2A stabilises this new RNA pseudoknot.

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Department of Biology

University of York

Wentworth Way

York

United Kingdom

YO10 5DD

Contact

+44 (0)1904 328688

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© 2026 Chris H. Hill

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