Instructions
This worksheet explores the fundamental biological process of protein synthesis. Read each question carefully and answer to the best of your ability. You will need to use the provided genetic code chart for Section 3.
Section 1: The Central Dogma - Fill in the Blanks
Complete the following paragraph using the words from the word bank below. Each word should be used only once.
The flow of genetic information in a cell is often described by the central dogma of molecular biology. The process begins in the 1. _______________ of a eukaryotic cell, where a segment of DNA is used as a template to create a molecule of messenger RNA (mRNA). This process is called 2. _______________ and is catalyzed by the enzyme 3. _______________. Before this mRNA molecule can leave the nucleus, it undergoes processing where non-coding regions called 4. _______________ are removed, while the coding regions, known as 5. _______________, are spliced together. The mature mRNA then travels to the cytoplasm and attaches to a 6. _______________. Here, the process of 7. _______________ occurs. The genetic code on the mRNA is read in three-base units called 8. _______________. Molecules of transfer RNA (tRNA) have a corresponding three-base unit called an 9. _______________ and carry a specific 10. _______________. As the ribosome moves along the mRNA, these building blocks are linked together to form a 11. _______________ chain, which will then fold into a functional protein.
Word Bank:
- Ribosome
- Amino Acid
- Transcription
- Exons
- Anticodon
- Polypeptide
- RNA Polymerase
- Translation
- Nucleus
- Codons
- Introns
Section 2: Comparing Processes
Answer the following questions with detailed explanations.
- Describe two key differences between transcription and translation in a eukaryotic cell. Consider their location, the molecules involved, and the final product.
- Explain the functional significance of removing introns from a pre-mRNA transcript. Why is this step crucial for creating a functional protein?
Section 3: From Gene to Protein
Use the DNA sequence and the genetic code chart below to answer the following questions.
Original DNA Template Strand: 3'-TAC GCT CCA TGG AAT ATC-5'
- Write the sequence of the complementary DNA coding strand.
- Transcribe the template strand into a sequence of mRNA.
- Translate the mRNA sequence from question 3b into a polypeptide chain of amino acids. Use the chart below. (Remember to look for start and stop signals).
- Mutation Analysis 1: A point mutation occurs in the original DNA template strand, changing the 11th base from G to C.
- a. Write the new mutated DNA template strand.
- b. Write the new mRNA sequence that would be transcribed from this mutated strand.
- c. What is the new amino acid sequence?
- d. What specific type of point mutation is this (silent, missense, or nonsense)? Explain your reasoning.
- Mutation Analysis 2: A different mutation occurs in the original DNA template strand, causing the 4th base (G) to be deleted.
- a. Write the resulting mRNA sequence. (Remember the reading frame will shift).
- b. What is this type of mutation called? Explain why it is often more detrimental than a point mutation.
The Genetic Code (mRNA Codons)
Second Base | |||||
---|---|---|---|---|---|
U | C | A | G | ||
First Base |
UUU Phe UUC Phe UUA Leu UUG Leu |
UCU Ser UCC Ser UCA Ser UCG Ser |
UAU Tyr UAC Tyr UAA STOP UAG STOP |
UGU Cys UGC Cys UGA STOP UGG Trp |
U C A G |
CUU Leu CUC Leu CUA Leu CUG Leu |
CCU Pro CCC Pro CCA Pro CCG Pro |
CAU His CAC His CAA Gln CAG Gln |
CGU Arg CGC Arg CGA Arg CGG Arg |
U C A G |
|
AUU Ile AUC Ile AUA Ile AUG Met (START) |
ACU Thr ACC Thr ACA Thr ACG Thr |
AAU Asn AAC Asn AAA Lys AAG Lys |
AGU Ser AGC Ser AGA Arg AGG Arg |
U C A G |
|
GUU Val GUC Val GUA Val GUG Val |
GCU Ala GCC Ala GCA Ala GCG Ala |
GAU Asp GAC Asp GAA Glu GAG Glu |
GGU Gly GGC Gly GGA Gly GGG Gly |
U C A G |
Answer Key
Section 1: The Central Dogma - Fill in the Blanks
- Nucleus
- Transcription
- RNA Polymerase
- Introns
- Exons
- Ribosome
- Translation
- Codons
- Anticodon
- Amino Acid
- Polypeptide
Section 2: Comparing Processes
-
Possible answers include (any two):
- Location: Transcription occurs in the nucleus, whereas translation occurs in the cytoplasm on a ribosome.
- Template: Transcription uses a DNA strand as a template, whereas translation uses an mRNA strand as a template.
- Enzyme/Machinery: Transcription is catalyzed by RNA polymerase, while translation is carried out by ribosomes and tRNA.
- Product: The product of transcription is an RNA molecule (pre-mRNA), while the product of translation is a polypeptide chain (protein).
- Introns are non-coding sequences that interrupt the genetic code for a protein. Removing them (splicing) is crucial because if they were left in the mature mRNA, the ribosome would try to translate them. This would introduce incorrect amino acids and shift the entire reading frame for the rest of the sequence, resulting in a completely different and almost certainly non-functional protein. Splicing ensures that only the correct, protein-coding exons are joined together to form a coherent genetic message.
Section 3: From Gene to Protein
- Complementary DNA coding strand:
5'-ATG CGA GGT ACC TTA TAG-3'
- Transcribed mRNA:
5'-AUG CGA GGU ACC UUA UAG-3'
- Polypeptide chain: Met - Arg - Gly - Thr - Leu - STOP. (The chain terminates at the UAG stop codon).
- Mutation Analysis 1:
- a. New mutated DNA template strand:
3'-TAC GCT CCA TCG AAT ATC-5'
- b. New mRNA sequence:
5'-AUG CGA GGU AGC UUA UAG-3'
- c. New amino acid sequence: Met - Arg - Gly - Ser - Leu - STOP.
- d. Type of mutation: This is a missense mutation. The change in a single nucleotide (G to C in the DNA, resulting in ACC to AGC in the mRNA) led to the incorporation of a different amino acid (Threonine to Serine) in the polypeptide chain.
- a. New mutated DNA template strand:
- Mutation Analysis 2:
- a. Resulting mRNA sequence:
5'-AUG CGA GUA CCU UAU AG...-3'
- b. Type of mutation: This is a frameshift mutation (specifically, a deletion). It is often more detrimental because deleting a single base shifts the entire reading frame for all subsequent codons. This scrambles the entire amino acid sequence from the point of the mutation onward, usually leading to a premature stop codon or a completely non-functional protein. It has a much more widespread effect than a single amino acid substitution.
- a. Resulting mRNA sequence: