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Updated: Mar 1, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
Published on: June 24, 2021
Alternative splicing shapes transcriptome but not proteome diversity in Physcomitrella patens
Igor Fesenko1, Regina Khazigaleeva2, Ilya Kirov2,3
1Laboratory of Proteomics, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia. fesigor@gmail.com.
Alternative splicing (AS) has a minor effect on proteome diversity in Physcomitrella patens. Long non-coding RNAs may regulate gene expression and AS, with specific hormones impacting AS responses.
Area of Science:
- Plant molecular biology
- Transcriptomics and proteomics
- Gene regulation
Background:
- Alternative splicing (AS) significantly influences eukaryotic cell transcriptome and proteome.
- Understanding AS in different life stages and cell types is crucial for deciphering gene expression complexity.
Purpose of the Study:
- To analyze alternative splicing (AS) in protonemata, gametophores, and protoplasts of Physcomitrella patens.
- To assess the contribution of AS to proteome diversity.
- To investigate the role of long non-coding RNAs (lncRNAs) and hormone treatments in AS regulation.
Main Methods:
- Transcriptome and proteome profiling
- Identification of alternatively spliced genes
- Analysis of lncRNA binding sites
- Hormone treatment experiments (abscisic acid and methyl jasmonic acid)
Main Results:
- 12,043 genes were identified as subject to alternative splicing.
- Alternative splicing has a limited impact on proteome diversity.
- Thousands of complementary binding sites for lncRNAs were found on mRNAs and pre-mRNAs.
- Abscisic acid and methyl jasmonic acid treatments induced isoform-specific responses in serine/arginine-rich (SR) genes.
Conclusions:
- AS contributes minimally to proteome diversity in Physcomitrella patens.
- lncRNAs represent a potential regulatory layer for gene expression and AS.
- Specific plant hormones (ABA and MeJA) differentially regulate AS and SR gene transcription in distinct cell types.
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