DNA to Protein & Mutation Lab
Follow the central dogma of molecular biology from DNA through mRNA to protein. Explore reading frames, codon translation, and how different types of mutations affect protein structure.
Guided Experiment: Central Dogma and Codon Reading
How does the reading frame affect the protein produced from the same DNA sequence? Will shifting the reading frame by one base produce a completely different protein?
Write your hypothesis in the Lab Report panel, then click Next.
Controls
12 bases (4 complete codons). Only A, T, G, C accepted.
Central Dogma
Codon Table
Data Table
(0 rows)| # | Trial | DNA Sequence | mRNA | Protein | Length (aa) | Mutation Type | Changed Positions |
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Reference Guide
Transcription
Transcription copies the DNA template strand into messenger RNA (mRNA). RNA polymerase reads the template 3' to 5' and builds the mRNA 5' to 3'. Each thymine (T) in DNA becomes uracil (U) in RNA.
The coding strand has the same sequence as the mRNA (with T instead of U) and runs antiparallel to the template strand.
Translation and the Codon Table
Ribosomes read mRNA in three-base units called codons. Each codon specifies one amino acid. Translation begins at the start codon AUG (methionine) and ends at a stop codon (UAA, UAG, or UGA).
The genetic code is degenerate, meaning multiple codons can encode the same amino acid. For example, both GAG and GAA code for glutamic acid (Glu). This redundancy helps buffer against harmful mutations.
Reading Frames
An mRNA sequence can be read in three different reading frames depending on the starting position. Each frame groups the bases into completely different codons, producing different proteins.
The start codon AUG establishes the correct reading frame for translation. Only one frame produces the intended protein.
Mutation Types
Point mutations change a single base pair. They are classified by their effect on the protein.
- Silent - DNA changes but the amino acid stays the same (wobble position)
- Missense - One amino acid is replaced by another (e.g., sickle cell: Glu to Val)
- Nonsense - A codon becomes a premature stop codon, truncating the protein
Frameshift mutations result from insertions or deletions that shift the reading frame. Every codon downstream is altered, usually producing a nonfunctional protein.