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Protein-protein Interactions Visualized by Bimolecular Fluorescence Complementation in Tobacco Protoplasts and Leaves
Published on: March 9, 2014
Mutagenesis Scanning Uncovers Evolutionary Constraints on Tobacco Etch Potyvirus Membrane-Associated 6K2 Protein
Rubén González1, Beilei Wu2,3, Xianghua Li4
1Instituto de Biología Integrativa de Sistemas (I2SysBio), CSIC-Universitat de València, València, Spain.
Abstract:
RNA virus high mutation rate is a double-edged sword. At the one side, most mutations jeopardize proteins functions; at the other side, mutations are needed to fuel adaptation. The relevant question then is the ratio between beneficial and deleterious mutations. To evaluate this ratio, we created a mutant library of the 6K2 gene of tobacco etch potyvirus that contains every possible single-nucleotide substitution. 6K2 protein anchors the virus replication complex to the network of endoplasmic reticulum membranes. The library was inoculated into the natural host Nicotiana tabacum, allowing competition among all these mutants and selection of those that are potentially viable. We identified 11 nonsynonymous mutations that remain in the viral population at measurable frequencies and evaluated their fitness. Some had fitness values higher than the wild-type and some were deleterious. The effect of these mutations in the structure, transmembrane properties, and function of 6K2 was evaluated in silico. In parallel, the effect of these mutations in infectivity, virus accumulation, symptoms development, and subcellular localization was evaluated in the natural host. The α-helix H1 in the N-terminal part of 6K2 turned out to be under purifying selection, while most observed mutations affect the link between transmembrane α-helices H2 and H3, fusing them into a longer helix and increasing its rigidity. In general, these changes are associated with higher within-host fitness and development of milder or no symptoms. This finding suggests that in nature selection upon 6K2 may result from a tradeoff between within-host accumulation and severity of symptoms.
Insights
RNA virus mutations offer adaptation but can harm protein function. This study analyzed mutations in tobacco etch potyvirus 6K2 gene, finding some enhance fitness and alter protein structure, leading to milder symptoms.
Area of Science:
- Virology
- Molecular Biology
- Plant Pathology
Background:
- RNA viruses possess high mutation rates, a double-edged sword providing adaptation but risking protein function loss.
- Understanding the balance between beneficial and deleterious mutations is crucial for RNA virus evolution and control.
Purpose of the Study:
- To determine the ratio of beneficial to deleterious mutations in the tobacco etch potyvirus 6K2 gene.
- To investigate the structural and functional consequences of 6K2 mutations in its natural host.
Main Methods:
- Generated a comprehensive mutant library of the 6K2 gene with all possible single-nucleotide substitutions.
- Inoculated the mutant library into Nicotiana tabacum to allow natural selection and competition.
- Evaluated mutation fitness, protein structure, transmembrane properties, infectivity, virus accumulation, and symptom development.
Main Results:
- Identified 11 nonsynonymous mutations with measurable frequencies, exhibiting varying fitness levels compared to wild-type.
- Observed that most mutations alter the link between transmembrane helices H2 and H3, increasing helix rigidity.
- Found that these structural changes correlate with increased within-host fitness and milder or absent disease symptoms.
Conclusions:
- The N-terminal α-helix H1 of 6K2 is under purifying selection.
- Mutations in 6K2 can enhance viral fitness within the host.
- A potential trade-off exists between within-host virus accumulation and disease severity, influencing natural selection on 6K2.
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