98%
921
2 minutes
20
Recent ribosome profiling and proteomic studies have revealed the presence of thousands of novel coding sequences, referred to as small open reading frames (sORFs), in prokaryotic and eukaryotic genomes. These genes have defied discovery via traditional genomic tools not only because they tend to be shorter than standard gene annotation length cutoffs, but also because they are, as a class, enriched in sequence properties previously assumed to be unusual, including non-AUG start codons. In this review, we summarize what is currently known about the incidence, efficiency, and mechanism of non-AUG start codon usage in prokaryotes and eukaryotes, and provide examples of regulatory and functional sORFs that initiate at non-AUG codons. While only a handful of non-AUG-initiated novel genes have been characterized in detail to date, their participation in important biological processes suggests that an improved understanding of this class of genes is needed.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256928 | PMC |
http://dx.doi.org/10.1016/j.yexcr.2020.111973 | DOI Listing |
Nat Struct Mol Biol
July 2025
Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Human translation initiation requires accurate recognition of translation start sites. While AUG codons are canonical start sites, non-AUG codons are also used, typically with lower efficiency. The initiator tRNA and initiation factors eIF1 and eIF5 control recognition.
View Article and Find Full Text PDFWhile protein synthesis typically initiates at an optimal AUG start codon, the 5' untranslated region (5'UTR) of mRNAs harbors non-canonical start codons that result in the translation of upstream Open Reading Frames (uORFs). However, the mechanisms underlying the selection of non-canonical start codons remain poorly understood. Structural analysis of translation pre-initiation complexes showed that the 2'OH group of the first nucleotide within start codons is monitored by 18S rRNA, allowing optimal translation initiation.
View Article and Find Full Text PDFElife
May 2025
Department of Gene Expression, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Uniwersytetu Poznańskiego 6, Poznan, Poland.
Expansion of CGG repeats (CGGexp) in the 5' untranslated region (5'UTR) of the gene underlies the fragile X premutation-associated conditions including tremor/ataxia syndrome, a late-onset neurodegenerative disease and fragile X-associated primary ovarian insufficiency. One common pathomechanism of these conditions is the repeat-associated non-AUG-initiated (RAN) translation of CGG repeats of mutant mRNA, resulting in production of FMRpolyG, a toxic protein containing long polyglycine tract. To identify novel modifiers of RAN translation we used an RNA-tagging system and mass spectrometry-based screening.
View Article and Find Full Text PDFExp Anim
May 2025
Laboratory of Biomedical Science, Department of Veterinary Medical Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo.
Translation regulation is crucial for cellular homeostasis. Recent studies have demonstrated that, in addition to the conventional AUG start codon, eukaryotic mRNA can also possess non-canonical start codons. These non-canonical start codons, including non-AUG codons, can be found both upstream and downstream of the conventional AUG start codon.
View Article and Find Full Text PDFRNA Biol
December 2025
School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
Dysregulated translation is a hallmark of cancer, and recent genome-wide studies in tumour cells have uncovered widespread translation of non-canonical reading frames that often initiate at non-AUG codons. If an upstream non-canonical start site is located within a frame with an annotated coding sequence (CDS), such translation events can lead to the production of proteoforms with altered N-termini (PANTs). Certain examples of PANTs from oncogenes (e.
View Article and Find Full Text PDF