# A reliable and quick method for screening alternative splicing variants for low-abundance genes

## TL;DR

This paper introduces a reliable and cost-effective method to identify alternative splicing variants, especially in low-abundance genes, using RT-nested PCR with gene-specific primers.

## Contribution

The novel contribution is an RT-nested PCR method that efficiently detects rare splicing variants, overcoming limitations of existing high-throughput and EST-based approaches.

## Key findings

- The method successfully identified three new splicing variants in the bdnf, trkc, and glb-18 genes.
- The RT-nested PCR approach is reliable, cost-effective, and suitable for detecting low-abundance gene transcripts.
- This technique enables the discovery of novel isoforms, which can aid in studying aberrant splicing in diseases.

## Abstract

Alternative splicing (AS) is a universal phenomenon in eukaryotes, and it is still challenging to identify AS events. Several methods have been developed to identify AS events, such as expressed sequence tags (EST), microarrays and RNA-seq. However, EST has limitations in identifying low-abundance genes, while microarray and RNA-seq are high-throughput technologies, and PCR-based technology is needed for validation. To overcome the limitations of EST and shortcomings of high-throughput technologies, we established a method to identify AS events, especially for low-abundance genes, by reverse transcription (RT) PCR with gene-specific primers (GSPs) followed by nested PCR. This process includes two major steps: 1) the use of GSPs to amplify as long as the specific gene segment and 2) multiple rounds of nested PCR to screen the AS and confirm the unknown splicing variants. With this method, we successfully identified three new splicing variants, namely, GenBank Accession No. HM623886 for the bdnf gene (GenBank GeneID: 12064), GenBank Accession No. JF417977 for the trkc gene (GenBank GeneID: 18213) and GenBank Accession No. HM623888 for the glb-18 gene (GenBank GeneID: 172485). In addition to its reliability and simplicity, the method is also cost-effective and labor-intensive. In conclusion, we developed an RT-nested PCR method using gene-specific primers to efficiently identify known and novel AS variants. This approach overcomes the limitations of existing methods for detecting rare transcripts. By enabling the discovery of new isoforms, especially for low-abundance genes, this technique can aid research into aberrant splicing in disease. Future studies can apply this method to uncover AS variants involved in cancer, neurodegeneration, and other splicing-related disorders.