Given the paucity of hits, we were not surprised that gene set enrichment analysis (GSEA) indicated no significant pathway enrichment in the cells expressing the 3-1 tRNA mutant, while only marginally significant enrichment of cell proliferation pathways related to vasculature and kidney development was found for the 4-1 nonsense suppressor, primarily driven by increased EGR1 expression rather than broader changes to the levels of multiple nodes across the associated pathways ( Supplementary Table S3 ).
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High-fidelity and differential nonsense suppression in live cells and a frontotemporal dementia allele with human transfer RNAs.
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