Abstract
Due to the redundancy of the genetic code most amino acids are encoded by multiple synonymous codons. It has been proposed that a biased frequency of synonymous codons can affect the function of proteins by modulating distinct steps in transcription, translation and folding. Here, we use two similar prototype K+ channels as model systems to examine whether codon choice has an impact on protein sorting. By monitoring transient expression of GFP-tagged channels in mammalian cells, we find that one of the two channels is sorted in a codon and cell cycle-dependent manner either to mitochondria or the secretory pathway. The data establish that a gene with either rare or frequent codons serves, together with a cell-state-dependent decoding mechanism, as a secondary code for sorting intracellular membrane proteins.
Original language | English (US) |
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Article number | 1128 |
Journal | Cells |
Volume | 10 |
Issue number | 5 |
DOIs | |
State | Published - May 2021 |
Keywords
- Codon usage
- Dual sorting
- Effect of synonymous codon exchange
- Membrane protein sorting
ASJC Scopus subject areas
- General Medicine