DeepKINET: a deep generative model for estimating single-cell RNA splicing and degradation rates
Messenger RNA splicing and degradation are critical for gene expression regulation, the abnormality of which leads to diseases. Previous methods for estimating kinetic rates have limitations, assuming uniform rates across cells. DeepKINET is a deep generative model that estimates splicing and degradation rates at single-cell resolution from scRNA-seq data. DeepKINET outperforms existing methods on simulated and metabolic labeling datasets. Applied to forebrain and breast cancer data, it identifies RNA-binding proteins responsible for kinetic rate diversity. DeepKINET also analyzes the effects of splicing factor mutations on target genes in erythroid lineage cells. DeepKINET effectively reveals cellular heterogeneity in post-transcriptional regulation.
Authors
- Teppei Shimamura (ORCID: https://orcid.org/0000-0003-2994-872X)
- Shuto Hayashi (ORCID: https://orcid.org/0000-0002-1623-0738)
- Chikara Mizukoshi (ORCID: https://orcid.org/0009-0009-4489-4636)
- Satoshi Nomura (ORCID: https://orcid.org/0000-0002-8678-4234)
- Yasuhiro Kojima (ORCID: https://orcid.org/0000-0002-1363-7153)
- Ko Abe (ORCID: https://orcid.org/0000-0002-0489-8677)
Institutions
- Tokyo Medical and Dental University (JP)
- Nagoya University Hospital (JP)
- National Cancer Research Institute (GB)
- Nagoya University (JP)
Publication Details
- Journal
- Genome biology
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1186/s13059-024-03367-8
- Citations
- 5
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 1.17
Funders
- Japan Agency for Medical Research and Development
- Tokyo Medical and Dental University
- Japan Society for the Promotion of Science
- Moonshot Research and Development Program