1. On paper, write out the first 30 bases in the middle of the page in order.  You want ensure you get them all in one line, with room to write more information around them.   2. Fill in the complementary base for each of the 30 bases.  Label this series of letters  “Complementary Bases” on the paper.  When you are done, you should have a complete  double-helix section of DNA. 3. On the opposite side of the original sequence (opposite from where you did the  complementary strand), translate the original sequence into mRNA.  Label this sequence as mRNA.

Biology (MindTap Course List)
11th Edition
ISBN:9781337392938
Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
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Chapter12: Dna: The Carrier Of Genetic Information
Section: Chapter Questions
Problem 4TYU: The two complementary strands of the DNA double helix are held to each other by (a) ionic bonds...
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1. On paper, write out the first 30 bases in the middle of the page in order.  You want ensure you get them all in one line, with room to write more information around them.  
2. Fill in the complementary base for each of the 30 bases.  Label this series of letters 
“Complementary Bases” on the paper.  When you are done, you should have a complete 
double-helix section of DNA.
3. On the opposite side of the original sequence (opposite from where you did the 
complementary strand), translate the original sequence into mRNA.  Label this sequence as mRNA.
4. Translate the mRNA strand into amino acids using your codon table.  You only need to 
record the 3-letter code for each amino acid.  Label this line as “Amino Acids.”  Record this sequence in your lab report (question 8).
5. Take a picture of your completed diagram for your lab report.  

Part 2 – Mutations

You will use the same 30-base sequence you started with for this section.

1. Write out the original 30-base DNA sequence on a new paper.
2. Change the 18th base pair from “A” to a “T” and the 22nd base from “G” to “A.”  These 
changes represent what happens when a substitution mutation occurs.
3. Transcribe the new sequence into RNA and translate it into amino acids.  Label your results on the page and record the amino acid sequence in your lab report.
4. Write out the original 30-base DNA sequence on a new paper.
5. Remove the 8th base and add a “T” at the end of the 30-base sequence, resulting in a new 30-base sequence (the T is the 31st or next base in the original gene sequence).  This represents a type of frameshift mutation: a deletion.
6. Transcribe the new sequence into RNA and translate it into amino acids.  Label your results on 
the page and record the amino acid sequence in your lab report.
7. Write out the original 30-base DNA sequence on a new paper.
8. Add a “T” after the 11th base (between the C and A), resulting in a 31-base sequence, but we will only use the first 30.  This represents a second type of frameshift mutation: an addition.

Transcribe the new sequence into RNA and translate it into amino acids.  Label your results on the page and record the amino acid sequence in your lab report.

10. Take a picture of your mutation transcription results (1 picture with all three works) and 
answer the questions.

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