ArticleGenomics, proteomics & bioinformatics2025
Differential Evolution of CDS and UTR Non-canonical RNA G-quadruplex Structures in Eukaryotic Transcriptomes.
Article in Genomics, proteomics & bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
RNA G-quadruplexes (rG4s) are non-classical, four-stranded secondary RNA structures that play regulatory roles in various biological processes. Although canonical rG4s have been studied extensively, recent advancements have underscored the importance of non-canonical rG4s. In this study, we experimentally determined rG4 structures from multiple eukaryotic species. Bioinformatic analysis revealed that across 1 billion years of evolution, rG4s have comprised an integral feature of eukaryotic transcriptomes; additionally, non-canonical rG4s consistently were found to dominate the surveyed rG4omes. Over time, the overall size of the rG4ome has expanded progressively, accompanied by a notable compositional shift such that untranslated region (UTR) rG4s became favored over protein coding sequence (CDS) rG4s. Additionally, we observed distinct evolutionary patterns for CDS and UTR rG4s, which involved differential evolutionary origins and canonicality drift patterns. Our findings suggest that new UTR rG4 sequences emerge rapidly during early mammalian evolution, whereas the more gradual increase in CDS rG4s is linked to changes in selective amino acid residue preferences. This plausible theory accounts for both the prevalence of UTR rG4s and the emergence of canonical motifs in mammalian models. Access to all the rG4 structures identified in this study is available through the rG4-seq Database application at https://rg4s.science/.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.