Human MutationGeneticsPeer-reviewed journal article
First estimation of the scale of canonical 5’ splice site GT>GC mutations generating wild-type transcripts and their medical genetic implications
Jin‐Huan LiniD, Xin‐Ying TangiD, Arnaud BoullingiD, Wen‐Bin ZouiD, Emmanuelle MassoniD, Yann FichouiD, Loann RaudiD, Marlène Le TertreiD, Shun‐Jiang DengiD, Isabelle Berlivet, Chandran KaiD, Matthew E. MortiD, Matthew HaydeniD, Raphaël LemaniD, Claude HoudayeriD, Gérald Le GaciD, D.N. CooperiD, Zhao‐Shen LiiD, Claude FéreciD, Zhuan LiaoiD, Jian‐Min CheniD
Abstract
It has long been known that canonical 5 splice site (5SS) GT>GC mutations may be compatible with normal splicing. However, to date, the true scale of canonical 5SS GT>GC mutations generating wild-type transcripts, both in the context of the frequency of such mutations and the level of wild-type transcripts generated from the mutation alleles, remain unknown. Herein, combining data derived from a meta-analysis of 45 informative disease-causing 5SS GT>GC mutations (from 42 genes) and a cell culture-based full-length gene splicing assay of 103 5SS GT>GC mutations (from 30 genes), we estimate that [~]15-18% of the canonical GT 5SSs are capable of generating between 1 and 84% normal transcripts as a consequence of the substitution of GT by GC. We further demonstrate that the canonical 5SSs whose substitutions of GT by GC generated normal transcripts show stronger complementarity to the 5 end of U1 snRNA than those sites whose substitutions of GT by GC did not lead to the generation of normal transcripts. We also observed a correlation between the generation of wild-type transcripts and a milder than expected clinical phenotype but found that none of the available splicing prediction tools were able to accurately predict the functional impact of 5SS GT>GC mutations. Our findings imply that 5SS GT>GC mutations may not invariably cause human disease but should also help to improve our understanding of the evolutionary processes that accompanied GT>GC subtype switching of U2-type introns in mammals.
- organism: human
- assay: DNA methylation
- research focus: differential expression
- approach: statistical model
- Citations
- 46
- FWCI
- 0.40
- Field percentile
- 37th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- 5’ splice site GC>GT variants differ from GT>GC variants in terms of their functionality and pathogenicity
Jin‐Huan Lin, Emmanuelle Masson, … Jian‐Min Chen·Human MutationPeer-reviewed·May 5, 2020
- The experimentally obtained functional impact assessments of GT>GC 5' splice site variants differ markedly from those predicted
Jian‐Min Chen, Jin‐Huan Lin, … Matthew Hayden·Current GenomicsPeer-reviewed·Feb 10, 2020
- When splicing is not all or none: GT>GC 5' splice-site variants as a model for intermediate effects and challenges in variant classification
Jin‐Huan Lin, Hao Wu, … Jian-Min Chen·Human Genetics and Genomics AdvancesPeer-reviewed·Apr 2, 2026
- U5 snRNA interactions with exons ensure splicing precision
Olga V. Artemyeva-Isman, Andrew C.G. Porter·Frontiers in GeneticsPeer-reviewed·Jul 2, 2021
- Animal, fungi, and plant genome sequences harbour different non-canonical splice sites
Katharina Sielemann, Boas Pucker·CellsPeer-reviewed·Feb 18, 2020
- In-Silico Characterization of TP53 Splice Mutations in Somatic and Germline Tumours
Apeksha Arun Bhandarkar, Noah Ethan Kelly-Foleni, … Sunali Y. Mehta·International Journal of Molecular SciencesPeer-reviewed·Dec 16, 2025