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Updated: Jun 9, 2026

Quantitative Analysis of Alternative Pre-mRNA Splicing in Mouse Brain Sections Using RNA In Situ Hybridization Assay
Published on: August 26, 2018
A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina
Lev Prasov1, Nadean L Brown, Tom Glaser
1Departments of Human Genetics and Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
Abstract:
The Math5 (Atoh7) gene is transiently expressed during retinogenesis by progenitors exiting mitosis, and is essential for ganglion cell (RGC) development. Math5 contains a single exon, and its 1.7 kb mRNA encodes a 149-aa polypeptide. Mouse Math5 mutants have essentially no RGCs or optic nerves. Given the importance of this gene in retinal development, we thoroughly investigated the possibility of Math5 mRNA splicing by Northern blot, 3'RACE, RNase protection assays, and RT-PCR, using RNAs extracted from embryonic eyes and adult cerebellum, or transcribed in vitro from cDNA clones. Because Math5 mRNA contains an elevated G+C content, we used graded concentrations of betaine, an isostabilizing agent that disrupts secondary structure. Although approximately 10% of cerebellar Math5 RNAs are spliced, truncating the polypeptide, our results show few, if any, spliced Math5 transcripts exist in the developing retina (<1%). Rare deleted cDNAs do arise via RT-mediated RNA template switching in vitro, and are selectively amplified during PCR. These data differ starkly from a recent study (Kanadia and Cepko 2010), which concluded that the vast majority of Math5 and other bHLH transcripts are spliced to generate noncoding RNAs. Our findings clarify the architecture of the Math5 gene and its mechanism of action. These results have implications for all members of the bHLH gene family, for any gene that is alternatively spliced, and for the interpretation of all RT-PCR experiments.
Insights
The Math5 (Atoh7) gene is crucial for retinal ganglion cell (RGC) development. Our study found minimal Math5 mRNA splicing in the retina, clarifying its gene architecture and mechanism of action.
Area of Science:
- Molecular Biology
- Developmental Biology
- Genetics
Background:
- The Math5 (Atoh7) gene is vital for retinal ganglion cell (RGC) development during retinogenesis.
- Math5 mRNA is essential for producing a functional polypeptide required for RGC formation.
Purpose of the Study:
- To investigate the extent of Math5 mRNA splicing in the developing retina.
- To clarify the transcript architecture and mechanism of action of the Math5 gene.
- To address conflicting findings regarding Math5 and other bHLH gene splicing.
Main Methods:
- Northern blot analysis
- 3'RACE (Rapid Amplification of cDNA Ends)
- RNase protection assays
- RT-PCR (Reverse Transcription Polymerase Chain Reaction)
- Use of betaine to disrupt RNA secondary structure
Main Results:
- While ~10% of cerebellar Math5 RNAs showed splicing, <1% of retinal Math5 transcripts were spliced.
- Rare deleted cDNAs arose from RT-mediated RNA template switching in vitro, amplified during PCR.
- Findings contradict a previous study suggesting widespread splicing of Math5 and other bHLH transcripts.
Conclusions:
- The vast majority of Math5 transcripts in the developing retina are not spliced.
- Clarifies the functional transcript architecture of the Math5 gene.
- Provides implications for understanding bHLH gene family function and interpreting RT-PCR experiments.
Related Concept Videos
RNA Splicing
Pre-mRNA Processing: RNA Splicing

