» Articles » PMID: 32966552

IsoResolve: Predicting Splice Isoform Functions by Integrating Gene and Isoform-level Features with Domain Adaptation

Overview
Journal Bioinformatics
Specialty Biology
Date 2020 Sep 23
PMID 32966552
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Motivation: High resolution annotation of gene functions is a central goal in functional genomics. A single gene may produce multiple isoforms with different functions through alternative splicing. Conventional approaches, however, consider a gene as a single entity without differentiating these functionally different isoforms. Towards understanding gene functions at higher resolution, recent efforts have focused on predicting the functions of isoforms. However, the performance of existing methods is far from satisfactory mainly because of the lack of isoform-level functional annotation.

Results: We present IsoResolve, a novel approach for isoform function prediction, which leverages the information from gene function prediction models with domain adaptation (DA). IsoResolve treats gene-level and isoform-level features as source and target domains, respectively. It uses DA to project the two domains into a latent variable space in such a way that the latent variables from the two domains have similar distribution, which enables the gene domain information to be leveraged for isoform function prediction. We systematically evaluated the performance of IsoResolve in predicting functions. Compared with five state-of-the-art methods, IsoResolve achieved significantly better performance. IsoResolve was further validated by case studies of genes with isoform-level functional annotation.

Availability And Implementation: IsoResolve is freely available at https://github.com/genemine/IsoResolve.

Supplementary Information: Supplementary data are available at Bioinformatics online.

Citing Articles

Toward a comprehensive profiling of alternative splicing proteoform structures, interactions and functions.

Laine E, Freiberger M Curr Opin Struct Biol. 2025; 90:102979.

PMID: 39778413 PMC: 7617313. DOI: 10.1016/j.sbi.2024.102979.


CrossIsoFun: predicting isoform functions using the integration of multi-omics data.

Liu Y, Li H, Wang J Bioinformatics. 2024; 41(1).

PMID: 39680906 PMC: 11706537. DOI: 10.1093/bioinformatics/btae742.


IsoFrog: a reversible jump Markov Chain Monte Carlo feature selection-based method for predicting isoform functions.

Liu Y, Yang C, Li H, Wang J Bioinformatics. 2023; 39(9).

PMID: 37647643 PMC: 10491952. DOI: 10.1093/bioinformatics/btad530.


An expectation-maximization framework for comprehensive prediction of isoform-specific functions.

Karlebach G, Carmody L, Sundaramurthi J, Casiraghi E, Hansen P, Reese J Bioinformatics. 2023; 39(4).

PMID: 36929917 PMC: 10079350. DOI: 10.1093/bioinformatics/btad132.


[Construction of an adenovirus vector expressing engineered splicing factor for regulating alternative splicing of YAP1 in neonatal rat cardiomyocytes].

Li Y, Zhao Q, Song X, Song J Nan Fang Yi Ke Da Xue Xue Bao. 2022; 42(7):1013-1018.

PMID: 35869763 PMC: 9308876. DOI: 10.12122/j.issn.1673-4254.2022.07.07.


References
1.
Pan Q, Shai O, Lee L, Frey B, Blencowe B . Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat Genet. 2008; 40(12):1413-5. DOI: 10.1038/ng.259. View

2.
Song Y, Botvinnik O, Lovci M, Kakaradov B, Liu P, Xu J . Single-Cell Alternative Splicing Analysis with Expedition Reveals Splicing Dynamics during Neuron Differentiation. Mol Cell. 2017; 67(1):148-161.e5. PMC: 5540791. DOI: 10.1016/j.molcel.2017.06.003. View

3.
Menon R, Roy A, Mukherjee S, Belkin S, Zhang Y, Omenn G . Functional implications of structural predictions for alternative splice proteins expressed in Her2/neu-induced breast cancers. J Proteome Res. 2011; 10(12):5503-11. PMC: 3230717. DOI: 10.1021/pr200772w. View

4.
Yang J, Yan R, Roy A, Xu D, Poisson J, Zhang Y . The I-TASSER Suite: protein structure and function prediction. Nat Methods. 2014; 12(1):7-8. PMC: 4428668. DOI: 10.1038/nmeth.3213. View

5.
Schmitz R, Young R, Ceribelli M, Jhavar S, Xiao W, Zhang M . Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics. Nature. 2012; 490(7418):116-20. PMC: 3609867. DOI: 10.1038/nature11378. View