Estimation of splicing metrics for NMD-sensitive transcripts
- 1Center for Bio and Medical Technologies, Moscow 121205, Russia
Abstract
Alternative splicing is commonly quantified using the Percent-Spliced-In (PSI) metric, which measures the relative abundances of alternatively spliced isoforms. However, some transcript isoforms are targeted by the nonsense-mediated mRNA decay (NMD) pathway, introducing a strong bias that leads to underestimation of their true splicing rates. To correct for this bias, we developed an analytical framework and a set of statistical models employing a linear fractional transformation that depends on a single parameter to capture the degradation rate of transcripts annotated as NMD targets relative to normal mRNA decay. Using Gaussian mixture models, we demonstrated a clear separation of splicing events into two classes, NMD-sensitive and NMD-evading, with the former exhibiting strong upregulation upon NMD inhibition and the latter showing little or no response. Moreover, NMD-evading events displayed higher coding potential and stronger translation signals both upstream and downstream of the stop codon, which are characteristic of NMD escape through translational readthrough. We further showed that incorporation of event-specific relative decay rates improves the interpretation of differential splicing patterns for transcripts annotated as NMD targets. In sum, our results provide a solid framework for corrected estimation of splicing metrics in NMD-targeted transcripts from short-read RNA-seq data.
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BibTeX
@misc{zavileyskiy2026estimation,
title = {{Estimation of splicing metrics for NMD-sensitive transcripts}},
author = {L. Zavileyskiy and M. Vlasenok and A. Kuznetsova and D. A. Skvortsov and D. D. Pervouchine},
howpublished = {bioRxiv},
year = {2026},
month = jun,
doi = {10.64898/2026.06.30.735642},
url = {https://www.biorxiv.org/content/10.64898/2026.06.30.735642v2},
note = {CC BY-NC},
}
RIS
TY - UNPB
TI - Estimation of splicing metrics for NMD-sensitive transcripts
AU - L. Zavileyskiy
AU - M. Vlasenok
AU - A. Kuznetsova
AU - D. A. Skvortsov
AU - D. D. Pervouchine
PY - 2026
DA - 2026/06/30
PB - bioRxiv
DO - 10.64898/2026.06.30.735642
UR - https://www.biorxiv.org/content/10.64898/2026.06.30.735642v2
AB - Alternative splicing is commonly quantified using the Percent-Spliced-In (PSI) metric, which measures the relative abundances of alternatively spliced isoforms. However, some transcript isoforms are targeted by the nonsense-mediated mRNA decay (NMD) pathway, introducing a strong bias that leads to underestimation of their true splicing rates. To correct for this bias, we developed an analytical framework and a set of statistical models employing a linear fractional transformation that depends on a single parameter to capture the degradation rate of transcripts annotated as NMD targets relative to normal mRNA decay. Using Gaussian mixture models, we demonstrated a clear separation of splicing events into two classes, NMD-sensitive and NMD-evading, with the former exhibiting strong upregulation upon NMD inhibition and the latter showing little or no response. Moreover, NMD-evading events displayed higher coding potential and stronger translation signals both upstream and downstream of the stop codon, which are characteristic of NMD escape through translational readthrough. We further showed that incorporation of event-specific relative decay rates improves the interpretation of differential splicing patterns for transcripts annotated as NMD targets. In sum, our results provide a solid framework for corrected estimation of splicing metrics in NMD-targeted transcripts from short-read RNA-seq data.
ER -