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- W3097113124 abstract "Global methods for assaying translation have greatly improved our understanding of the protein-coding capacity of the genome. In particular, it is now possible to perform genome-wide and condition-specific identification of translation initiation sites through modified ribosome profiling methods that selectively capture initiating ribosomes. Here we discuss our recent study applying such an approach to meiotic and mitotic timepoints in the simple eukaryote, budding yeast, as an example of the surprising diversity of protein products—many of which are non-canonical—that can be revealed by such methods. We also highlight several key challenges in studying non-canonical protein isoforms that have precluded their prior systematic discovery. A growing body of work supports expanded use of empirical protein-coding region identification, which can help relieve some of the limitations and biases inherent to traditional genome annotation approaches. Our study also argues for the adoption of less static views of gene identity and a broader framework for considering the translational capacity of the genome." @default.
- W3097113124 created "2020-11-09" @default.
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- W3097113124 date "2020-11-01" @default.
- W3097113124 modified "2023-09-24" @default.
- W3097113124 title "Rules are made to be broken: a “simple” model organism reveals the complexity of gene regulation" @default.
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- W3097113124 doi "https://doi.org/10.1007/s00294-020-01121-8" @default.
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