Evidence map›Paper›PMID 26802218›Full record

ArticleMolecular biology and evolution2016

Purifying Selection on Exonic Splice Enhancers in Intronless Genes.

Rosina Savisaar, Laurence D Hurst

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Exploring Disordered Regions of Human Spliceosome Proteins.The journal of physical chemistry letters · 2026
    Article
  2. Article
  3. Tumor-promoting effect and tumor immunity of SRSFs.Frontiers in cell and developmental biology · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Trends in the evolution of intronless genes inFrontiers in plant science · 2023
    Article
  8. SRSF1-mediated alternative splicing is required for spermatogenesis.International journal of biological sciences · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Rosina SavisaarDepartment of Biology and Biochemistry, The Milner Centre for Evolution, University of Bath, Bath, United Kingdom r.savisaar@bath.ac.uk.
Laurence D HurstDepartment of Biology and Biochemistry, The Milner Centre for Evolution, University of Bath, Bath, United Kingdom.

Funding

European Research Council 669207Medical Research Council MR/L007215/1
6 · The paper itself

Abstract

Exonic splice enhancers (ESEs) are short nucleotide motifs, enriched near exon ends, that enhance the recognition of the splice site and thus promote splicing. Are intronless genes under selection to avoid these motifs so as not to attract the splicing machinery to an mRNA that should not be spliced, thereby preventing the production of an aberrant transcript? Consistent with this possibility, we find that ESEs in putative recent retrocopies are at a higher density and evolving faster than those in other intronless genes, suggesting that they are being lost. Moreover, intronless genes are less dense in putative ESEs than intron-containing ones. However, this latter difference is likely due to the skewed base composition of intronless sequences, a skew that is in line with the general GC richness of few exon genes. Indeed, after controlling for such biases, we find that both intronless and intron-containing genes are denser in ESEs than expected by chance. Importantly, nucleotide-controlled analysis of evolutionary rates at synonymous sites in ESEs indicates that the ESEs in intronless genes are under purifying selection in both human and mouse. We conclude that on the loss of introns, some but not all, ESE motifs are lost, the remainder having functions beyond a role in splice promotion. These results have implications for the design of intronless transgenes and for understanding the causes of selection on synonymous sites.

Indexed as

Enhancer Elements, GeneticExonsIntronsRNA Splice SitesAnimalsComputational BiologyEvolution, MolecularHumansMiceMutationMutation RateNucleotide MotifsPolymorphism, Single NucleotideRNA SplicingSelection, GeneticRNA Splice Sitesavoidance selectionexonic splice enhancersintronless genessplice controlSR proteins

Identifiers

PMID26802218
PMCPMC4868121

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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.