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Egab, I.

Publications and source records attributed to Egab, I..

2 recordsLinked to original sources

Unveiling the Hidden Rules: Enhancing NMD Prediction for Protein-Truncating Variants

Nonsense-mediated decay (NMD) is a conserved RNA quality-control pathway that degrades transcripts containing premature termination codons. Because roughly a third of pathogenic variants in ClinVar can lead to truncated protein synthesis, predicting whether such transcripts undergo NMD is central to interpreting variant effects, yet the canonical 50-55 nucleotide rule explains only about half of observed outcome variability. Using paired whole-genome and RNA-sequencing from 10,306 individual samples in the Trans-Omics for Precision Medicine (TOPMed) program, we quantified NMD efficiency for 5,749 germline truncating variants via allele-specific expression and trained a gradient-boosting classifier, TrunCat, that distinguished NMD-sensitive from NMD-escape transcripts with [~]78% ROC-AUC (Receiver Operating Characteristic - Area Under the Curve). A reduced model using the ten features with the highest mean SHAP (SHapley Additive exPlanations) value as a measure of each features average contribution to predictions nearly matched this performance. Applied across large variant databases and a rare-disease cohort, the model produced NMD outcome predictions, with variants of uncertain significance showing higher predicted escape than pathogenic ones. This framework confirms the canonical rule, identifies non-canonical determinants, and offers a scalable resource for interpreting protein-truncating variants.

genomics↗

Genomic stop codon scanning reveals quantitative principles of nonsense-mediated mRNA decay

Nonsense-mediated mRNA decay (NMD) degrades transcripts containing premature termination codons (PTCs), critically shaping the disease outcomes of protein-truncating variants. While existing NMD rules categorize PTCs as NMD-triggering or NMD-evading, they cannot quantitatively predict the degree of NMD activity for a given endogenous PTC variant. To provide quantitative insight into NMD, we used saturation genome editing (SGE) to systematically introduce all possible PTCs (TAA, TAG, TGA) at every codon position spanning the first, penultimate, and three internal exons of the Lamin A/C (LMNA) gene. Combining targeted sequencing with NMD inhibition, we measured mRNA expression and NMD activity for 722 PTCs and 211 single nucleotide variants (SNVs). Our data validate known positional trends in NMD activity but reveal unexpected complexity. In the penultimate exon, the PTC position effect extends beyond the binary 50-55 nucleotides (nt) rule, revealing a quantitative relationship between the PTC-EJC distance and NMD activity. At the 5 end, NMD is completely absent in the first 21 codons of LMNA, followed by sharp activation over the next 4 codons. Both patterns, at the 5 end and in the penultimate exon, are unexplained by current models. Finally, internal exons show robust NMD with outliers consistently mapping to predicted readthrough-permissive sequence contexts, including the conserved readthrough promoting TGA-CT motif. This comprehensive dataset provides an unprecedented resource for understanding the quantitative impact of PTC position and sequence context on NMD, with direct implications for the clinical interpretation of nonsense variants in the human population.

genomics↗