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#pyrrolysine incorporation

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Selenocysteine and pyrrolysine incorporation represent

Selenocysteine and pyrrolysine incorporation exemplify programmed recoding events where stop codons acquire sense meaning through dedicated cis-elements and trans-factors rather than translational errors. Mechanisms involve competition with release factors RF1, RF2, eRF1, specialized tRNAs bearing UCA or CUA anticodons, unique elongation factors SelB, EFSec, and orthogonal synthetases PylRS plus mRNA signals SECIS or PYLIS. Recoding preserves genome-wide termination fidelity while permitting selective reassignment at specific loci. This represents evolutionary flexibility of genetic code, not

Ref: Alberts et al., Molecular Biology of the Cell, 7th ed., Chapter 6: Stop Codon Recoding as Genetic Code Expansion

Pyrrolysine incorporation is found mainly in

Pyrrolysine incorporation displays narrow phylogenetic distribution, predominantly encountered in methanogenic Euryarchaeota such as Methanosarcina barkeri, Methanococcus, Methanomassiliicoccales, and few anaerobic Gram-positive bacteria including Desulfitobacterium hafniense, Acetohalobium arabaticum, Thermincola. These organisms utilize methylated amines as methanogenesis substrates, requiring monomethylamine, dimethylamine, trimethylamine methyltransferases harboring pyrrolysine at catalytic site for methyl group transfer to corrinoid proteins. Genes pylTSBCD cluster in operon regulated by

Ref: NCBI Bookshelf, Comparative Genomics: Pyrrolysine Distribution in Archaea and Bacteria