# Methods for Analyzing Alternative Splicing and Its Regulation in Plants: From Gene‐Specific Approaches to Transcriptome‐Wide Studies

**Authors:** Stavros Vraggalas, Oussama Guennich, Boushra Shalha, Christos Bazakos, Hélène S. Robert, Olha Lakhneko, Sotirios Fragkostefanakis

PMC · DOI: 10.1111/ppl.70639 · Physiologia Plantarum · 2025-11-18

## TL;DR

This review discusses methods for studying alternative splicing in plants, from gene-specific techniques to transcriptome-wide approaches, emphasizing their roles in development and stress response.

## Contribution

The paper provides a comprehensive comparison of experimental methods for analyzing alternative splicing regulation in plants.

## Key findings

- Gene-specific assays like minigene and electrophoretic mobility shift assays help study splicing factor-RNA interactions.
- High-throughput methods enable identification of RNA-binding partners of splicing factors in plants.
- Transcriptome-wide approaches are crucial for understanding splicing profiles and their regulation in plant biology.

## Abstract

Precursor messenger RNA (pre‐mRNA) splicing is a fundamental mechanism of gene regulation that influences both mRNA abundance and proteome diversity. In plants, alternative splicing plays a critical role in coordinating development and enabling responses to environmental stress. This process is tightly regulated by the spliceosome and associated splicing factors, which recognize conserved sequence motifs in pre‐mRNAs to guide intron removal and exon joining. In this review, we summarize and compare experimental approaches used to analyze both the regulation of alternative splicing and the splicing profiles of genes, spanning from gene‐specific assays to transcriptome‐wide methods. Gene‐specific techniques, such as minigene assays, transient expression systems, electrophoretic mobility shift assays, and isothermal titration calorimetry, provide insights into the molecular interactions between splicing factors and their RNA targets. To identify RNA‐binding partners of splicing factors, or splicing factors that interact with a specific RNA, we discuss high‐throughput methods that can be applied in vivo and in vitro. By comparing these approaches, we highlight their advantages, limitations, and applications in plant biology. Understanding alternative splicing regulation is essential for deciphering its role in plant adaptation to environmental challenges, with potential implications for crop improvement strategies.

## Full-text entities

- **Genes:** pup-2 (PAP-associated domain-containing protein) [NCBI Gene 175708], pup-3 (PAP-associated domain-containing protein) [NCBI Gene 172207], APX1 (ascorbate peroxidase 1) [NCBI Gene 837304] {aka ASCORBATE PEROXIDASE, ATAPX01, ATAPX1, CS1, F24B9.2, F24B9_2}, AT4G16465 (tRNA-Thr) [NCBI Gene 3770152] {aka 68169.TRNA-THR-3}, SUGP1 (SURP and G-patch domain containing 1) [NCBI Gene 57794] {aka F23858, RBP, SF4}, PUP2 (purine permease 2) [NCBI Gene 817941] {aka ATPUP2, T1B8.6, T1B8_6, purine permease 2}, TERC (telomerase RNA component) [NCBI Gene 7012] {aka DKCA1, PFBMFT2, SCARNA19, TER, TR, TRC3}, MIRLET7A1 (microRNA let-7a-1) [NCBI Gene 406881] {aka LET7A1, MIRNLET7A1, let-7a-1}, adr-1 (A-to-I RNA editing regulator adr-1) [NCBI Gene 172542], MIR101-1 (microRNA 101-1) [NCBI Gene 406893] {aka MIRN101-1, mir-101-1}, FPA (RNA binding protein) [NCBI Gene 818942] {aka T1O24.15}, HOTAIR (HOX transcript antisense RNA) [NCBI Gene 100124700] {aka HOXAS, HOXC-AS4, HOXC11-AS1, NCRNA00072}, RAP (RAP) [NCBI Gene 817747] {aka ATRAP, F20M17.7, F20M17_7}
- **Diseases:** SJs (MESH:D020511), AS (MESH:C536589)
- **Chemicals:** acrylamide (MESH:D020106), oligonucleotides (MESH:D009841), biotin (MESH:D001710), LNA (MESH:C477371), carotenoids (MESH:D002338), phenol (MESH:D019800), cytosines (MESH:D003596), C (MESH:D002244), chlorophylls (MESH:D002734), TALON (MESH:C013418), uracils (MESH:D014498), uridines (MESH:D014529), acid (MESH:D000143), FAM (MESH:C031179), adenosine (MESH:D000241), inosine (MESH:D007288), polyA (MESH:D011061), flavonoids (MESH:D005419), Formaldehyde (MESH:D005557), heparin (MESH:D006493), glutaraldehyde (MESH:D005976), agarose (MESH:D012685), U (MESH:D014501), amino acid (MESH:D000596), desthiobiotin (MESH:C004749), 15N (-), H2O2 (MESH:D006861)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], C. elegans [taxon 328850], Astragalus membranaceus (species) [taxon 649199], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Caenorhabditis elegans (species) [taxon 6239], Glycine max (soybean, species) [taxon 3847], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Sorghum bicolor (broomcorn, species) [taxon 4558], Homo sapiens (human, species) [taxon 9606], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Brassica napus (oilseed rape, species) [taxon 3708], Solanum lycopersicum (tomato, species) [taxon 4081]
- **Mutations:** E488Q, Serine/Threonine, G9A

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12626760/full.md

## References

156 references — full list in the complete paper: https://tomesphere.com/paper/PMC12626760/full.md

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Source: https://tomesphere.com/paper/PMC12626760