bims-micpro Biomed News
on Discovery and characterization of microproteins
Issue of 2025–11–02
two papers selected by
Thomas Farid Martínez, University of California, Irvine



  1. ACS Synth Biol. 2025 Oct 27.
      We demonstrate a new synthetic genetic component for boosting translational levels in bacteria. Boosting is facilitated by a short and nonfunctional open reading frame (nfORF) that encodes a "nonsense" peptide located upstream of the target gene. The nfORF may be either in-frame or frame-shifted relative to the target open reading frame (tORF), and it contains an internal strong RBS that is immediately adjacent to its stop codon. We characterized 50 nfORFs, which allowed us to build a predictive model for the nfORF sequence, length, and distance from the tORF. Finally, we validated the model by testing three additional unseen nfORFs and demonstrated that the model also accurately predicts a translational boost for another target gene. Our results show how ribosome recruitment can be engineered to boost translation by as much as ×20 by precise engineering of an upstream nfORF. Our finding can be used for a variety of gene expression applications, by increasing expression for potentially any target gene that is produced in Escherichia coli.
    Keywords:  expression boost; nonfunctional open reading frame; ribosomal stretching; target open reading frame; translational coupling; translational reinitiation
    DOI:  https://doi.org/10.1021/acssynbio.5c00505
  2. PLoS Genet. 2025 Oct;21(10): e1011934
      Circular RNAs (circRNAs) are generally considered a new class of non-coding RNA (ncRNA) that frequently appears in the eukaryotic transcriptome. In principle, circRNAs may encode proteins, as some of them are generated from exons and possess elements for internal ribosome entry. Circular RNAs have the potential to serve as an unexplored reservoir for the generation of novel proteins, yet the identification of coding-circRNAs is a daunting task. In this study, we developed a specialized strategy for the discovery of coding-circRNA by combining RNA sequencing, ribosome profiling, and mass spectrometry to find a multitude of circRNAs translated in vivo. A total of 40,084 circRNAs were found in chicken myoblasts and myotubes, and 15,332 circRNAs had a predicted open reading frame (ORF). Via ribosome footprints, we discovered that a group of circRNAs (4,069) was associated with translating ribosomes (ribo-circRNAs). Moreover, a total of 3,927 circRNAs with an infinite ORF were discovered, and 860 of them were associated with translating ribosome (ribo-no-stop-codon circRNAs). Mass spectrometry found 5 specific peptides spectra spanning a back-splice junction of circRNAs. circSIK2, one of the ribo-circRNAs, could be methylated by METTL3 and translated into SIK2-176aa, thus promoting the proliferation and differentiation of myoblasts and muscle hypertrophy. Our results suggest that many circRNAs were translating during chicken myogenesis, and METTL3 could enhance the translation of circSIK2. To the best of our knowledge, only two circRNAs translation events have been reported to be mediated by m6A. Our research would represent the third such event, and the first documented instance of a translatable circRNA in poultry.
    DOI:  https://doi.org/10.1371/journal.pgen.1011934