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RNA Splicing

Join exons, remove an intron and compare the messages made from one gene.

Experimental post-catalytic human spliceosome cutaway with mint joined exons, a dark-green intron lariat and violet small nuclear RNAs surrounded by detailed grey protein machinery.
Structural reference

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Quick reference

The first transcript

A eukaryotic pre-mRNA can contain both exons and introns. Splicing removes introns and joins the retained exons. Exons can contain untranslated regions as well as protein-coding sequence.

An RNA machine

The spliceosome contains proteins and small nuclear RNAs. In the usual spliceosomal reaction, the intron forms a branched lariat intermediate before the flanking exons are joined.

Alternative outcomes

Regulated use of splice sites can produce different transcripts from a gene. Exon skipping may preserve or change a coding frame, depending on the boundaries. A real cell can produce a mixture of isoforms; the choices here are fixed teaching examples.

Check your understanding Optional

Does skipping an exon always cause a frameshift?

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At the bench

Inspect the experimental spliceosome structure used in the Cell tour.

Open Cell
Sources and model notes

Structure-based views of resolved experimental coordinates. Cutaways, category colours, camera choices and guided highlights are authored for teaching. Coordinates remain fixed; highlights are not experimental trajectories or simulation outputs.

RCSB PDB · Spliceosome 6QDV (opens a new tab)

Human post-catalytic complex with an experimental RNA substrate.

CSHL · Alternative RNA splicing (opens a new tab)

Researcher explanation of different transcript outcomes, including SMN2.