🧬 Molecular Biology Lab: Central Dogma (DNA → mRNA → Protein)

Edit the DNA nucleotide sequence or apply clinical mutations to observe live mRNA transcription and ribosomal translation into a polypeptide amino acid chain.

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Sequence Length 30 bp 10 full codons
GC Content (% GC) 53.3 % Double-helix thermal stability
Translated Amino Acids 9 AA STOP codon reached
Peptide Molecular Mass ~990 Da ~110 Daltons per residue
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How does the Central Dogma of Molecular Biology work?

First articulated by Francis Crick in 1958, the Central Dogma of Molecular Biology describes how genetic information flows inside living cells across two key stages: Transcription ($\text{DNA} \rightarrow \text{mRNA}$) in the nucleus and Translation ($\text{mRNA} \rightarrow \text{Protein}$) at the cytoplasmic ribosomes.

During transcription, RNA polymerase reads the template DNA strand in the $3' \rightarrow 5'$ direction and synthesizes a complementary messenger RNA strand ($5' \rightarrow 3'$) following Watson-Crick base pairing rules, except that Uracil ($\text{U}$) replaces Thymine ($\text{T}$) in RNA: $\text{A}\rightarrow\text{U}$, $\text{T}\rightarrow\text{A}$, $\text{C}\rightarrow\text{G}$, and $\text{G}\rightarrow\text{C}$.

During translation, the ribosome scans mRNA in three-nucleotide triplets called codons, typically starting at $\text{AUG}$ (Methionine) and linking amino acids via peptide bonds until encountering one of the three termination STOP codons ($\text{UAA}, \text{UAG}, \text{UGA}$).

Step-by-step guided experiment

1. Genetic Code Redundancy (Silent Mutation): Compare the Wild-Type Gene preset against Silent Mutation. Even though DNA base 18 mutates from $\text{C}$ to $\text{T}$ (changing the mRNA codon from $\text{GAG}$ to $\text{GAA}$), both triplets encode Glutamic Acid ($\text{Glu}$), leaving the protein sequence unchanged.

2. Sickle-Cell Anemia (Missense): Select Sickle-Cell Anemia. A single nucleotide swap ($\text{T} \rightarrow \text{A}$) in the sixth codon converts mRNA $\text{GAG}$ ($\text{Glu}$) into $\text{GUG}$ (Valine, $\text{Val}$).

Frequently Asked Questions (FAQ)

How do nitrogenous bases pair during DNA-to-mRNA transcription?

RNA polymerase reads the template DNA strand ($3' \rightarrow 5'$) and synthesizes messenger RNA ($5' \rightarrow 3'$) replacing Thymine with Uracil: Adenine ($\text{A}$) pairs with Uracil ($\text{U}$), Thymine ($\text{T}$) with Adenine ($\text{A}$), Cytosine ($\text{C}$) with Guanine ($\text{G}$), and Guanine ($\text{G}$) with Cytosine ($\text{C}$).

Why does a silent mutation leave the resulting protein unchanged?

Because the genetic code is degenerate (redundant): 64 possible three-letter codons encode just 20 amino acids and 3 stop signals. For instance, both $\text{GAA}$ and $\text{GAG}$ code for Glutamic Acid ($\text{Glu}$).

Which point mutation causes sickle-cell anemia?

A single-base missense substitution in the beta-globin gene changes the 6th mRNA codon from $\text{GAG}$ (hydrophilic Glutamic Acid) to $\text{GUG}$ (hydrophobic Valine), altering hemoglobin's structure.

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