Serviene E~Nagy PD, 2005

Pubmed ID 16027361
Title Genome-wide screen identifies host genes affecting viral RNA recombination.
Authors Elena Serviene, Natalia Shapka, Chi-Ping Cheng, Tadas Panavas, Bencharong Phuangrat, Jannine Baker, Peter D Nagy
Abstract Rapid evolution of RNA viruses with mRNA-sense genomes is a major concern to health and economic welfare because of the devastating diseases these viruses inflict on humans, animals, and plants. To test whether host genes can affect the evolution of RNA viruses, we used a Saccharomyces cerevisiae single-gene deletion library, which includes approximately 80% of yeast genes, in RNA recombination studies based on a small viral replicon RNA derived from tomato bushy stunt virus. The genome-wide screen led to the identification of five host genes whose absence resulted in the rapid generation of new viral RNA recombinants. Thus, these genes normally suppress viral RNA recombination, but in their absence, hosts become viral recombination "hotbeds." Four of the five suppressor genes are likely involved in RNA degradation, suggesting that RNA degradation could play a role in viral RNA recombination. In contrast, deletion of four other host genes inhibited virus recombination, indicating that these genes normally accelerate the RNA recombination process. A comparison of deletion strains with the lowest and the highest recombination rate revealed that host genes could affect recombinant accumulation by up to 80-fold. Overall, our results demonstrate that a set of host genes have a major effect on RNA virus recombination and evolution.
Citation Proc. Natl. Acad. Sci. U.S.A. 2005; 102:10545-50


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Papers Phenotype Conditions Collection Tested mutants Data Details
Serviene E~Nagy PD, 2005 viral RNA recombination standard [standard] hap a ~4,548 Discrete

Curation history

March 7, 2014 Tested strains requested.
March 7, 2014 Data waiting for tested.
May 14, 2014 Tested strains requested.
Nov. 11, 2014 Tested strains abandoned.
Nov. 11, 2014 Data to load.
Oct. 21, 2016 Data loaded.