D1.2.16 (HL)—Alternative splicing
Alternative splicing allows different exon combinations from one transcript to generate multiple mature mRNAs and protein variants in eukaryotic cells.
- Syllabus
- First assessment 2025
- Objective
- D1.2.16
- Level
- HL
Alternative splicing allows different exon combinations from one transcript to generate multiple mature mRNAs and protein variants in eukaryotic cells.

Coverage 2016–2020 · Updated 16 Jul 2026
Alternative splicing joins different combinations of exons from one pre-mRNA, allowing one gene to code for different polypeptides.
After introns are removed, selected exons can be retained or omitted in different mature mRNAs. Each exon combination creates a different codon sequence for translation.
One DNA gene → one pre-mRNA containing exons/introns → introns removed → different exon combinations joined → different mature mRNAs → polypeptide variants.
If mature mRNA A contains exons 1–2–3 and mature mRNA B contains exons 1–3, translation can produce two polypeptides from the same gene.
Alternative splicing changes RNA processing, not the DNA gene. Specific named protein examples or detailed splicing-factor mechanisms are not required.
This objective is assessed through multiple choice.
Build the answer around this relationship: Alternative splicing joins different exon combinations.
Assuming one gene can produce only one protein product in all circumstances.
Representative question
The number of protein-coding genes in the human genome is estimated to be about 20000 , which is much less than the size of the proteome. What is one reason for this?
Exons are removed from RNA before translation.
There are more types of amino acids than nucleotides.
mRNA can be spliced after transcription.
Base substitutions occur during transcription.
C
RNA polymerase reads template DNA 3' to 5' and synthesizes RNA 5' to 3'; ribosomes translate mRNA codons in the 5' to 3' direction. Promoters mark transcription start regions and orientation; transcription factors help RNA polymerase bind and initiate in eukaryotes. Non-coding DNA does not code for polypeptide amino acid sequences and includes introns, regulatory sequences, telomeres, rRNA genes, and tRNA genes. Eukaryotic pre-mRNA is modified before export and translation by adding a 5' cap and poly-A tail and removing introns by splicing. Alternative splicing joins different exon combinations from one pre-mRNA, so one gene can produce multiple protein variants in different cells or stages. Translation initiation assembles ribosomal subunits at the start codon AUG; initiator tRNA enters the P site and A, P, and E sites organize tRNA movement. Newly made polypeptides may be folded, cleaved, or chemically modified; preproinsulin processing to active insulin is a key example. Proteasomes degrade tagged, damaged, or unneeded proteins; amino acid recycling supports new protein synthesis and proteome quality control.