0% found this document useful (0 votes)
68 views2 pages

Asynchronous Activity in Science March 7

The document discusses different types of mutations including frameshift mutations caused by deletions or insertions of DNA bases, and point mutations caused by substitutions. It provides examples of mutated DNA sequences and asks the reader to determine the type of mutation and potential effects. Sickle cell anemia is used as an example where a single base substitution in the hemoglobin gene results in stiff, sickle-shaped red blood cells.

Uploaded by

xenareale
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
68 views2 pages

Asynchronous Activity in Science March 7

The document discusses different types of mutations including frameshift mutations caused by deletions or insertions of DNA bases, and point mutations caused by substitutions. It provides examples of mutated DNA sequences and asks the reader to determine the type of mutation and potential effects. Sickle cell anemia is used as an example where a single base substitution in the hemoglobin gene results in stiff, sickle-shaped red blood cells.

Uploaded by

xenareale
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 2

NAME __________________________________ Mutations Practice

(staff.fcps.net/einman/biology/MutationsWS.doc) Deletion, Insertion & Substitution

There are several types of mutation:


 Frameshift: DELETION (a base is lost/deleted)
 Frameshift: INSERTION (an extra base is added/inserted)
--- Deletion & insertion may cause what’s called a FRAMESHIFT mutation, meaning the reading “frame"
changes, thus changing the amino acid sequence from this point forward
 POINT MUTATION/SUBSTITUTION (one base is substituted for another)
--- If a substitution changes the amino acid, it’s called a MISSENSE mutation
--- If a substitution does not change the amino acid, it’s called a SILENT mutation
--- If a substitution changes the amino acid to a “stop,” it’s called a NONSENSE mutation

Complete the boxes below. Classify each as Frameshift (Deletion or Insertion) or Substitution.
. (Hint: Deletion & Insertion will always be frameshift).

Original DNA Sequence: T A C A C C T T G G C G A C G A C T…


mRNA Sequence:
Amino Acid Sequence:

Mutated DNA Sequence #1 T A C A T C T T G G C G A C G A C T…


What’s the mRNA sequence? (Circle the change)
What will be the amino acid sequence?
Will there likely be effects? What type of mutation is this? ________________________________

Mutated DNA Sequence #2 T A C G A C C T T G G C G A C G A C T…


What’s the mRNA sequence? (Circle the change)
What will be the amino acid sequence?
Will there likely be effects? What type of mutation is this? ________________________________

Mutated DNA Sequence #3 T A C A C C T T A G C G A C G A C T…


What’s the mRNA sequence? (Circle the change)
What will be the amino acid sequence?
Will there likely be effects? What type of mutation is this? ________________________________

Mutated DNA Sequence #4 T A C A C C T T G G C G A C T A C T…


What’s the mRNA sequence? (Circle the change)
What will be the amino acid sequence?
Will there likely be effects? What type of mutation is this? _________________________________
Original DNA Sequence: T A C A C C T T G G C G A C G A C T…
mRNA Sequence:
Amino Acid Sequence:

Mutated DNA Sequence #5 T A C A C C T T G G G A C G A C T…


What’s the mRNA sequence? (Circle the change)
What will be the amino acid sequence?
Will there likely be effects? What type of mutation is this? _________________________________

1. Which type of mutation is responsible for new variations of a trait?


2. Which type of mutation does not result in an abnormal amino acid sequence?
3. Which type of mutation stops the translation of an mRNA molecule? ______________________________________

Sickle Cell Anemia

Sickle cell anemia is the result of a type of mutation in the gene that codes for part of the hemoglobin molecule.

Recall that hemoglobin carries oxygen in your red bloods cells. The mutation causes these red blood cells to

become stiff & sickle-shaped when they release their oxygen. The sickled cells tend to get stuck in blood vessels,

causing pain and increased risk of stroke, blindness, damage to the heart & lungs, and other conditions.

--- Analyze the DNA strands below to determine what amino acid is changed AND what type of mutation occurred

Normal hemoglobin DNA C A C G T A G A C T G A G G A C T C…

Normal hemoglobin mRNA

Normal hemoglobin AA sequence

--------------------------------------------------------------------------------------------------------------------------------

Sickle cell hemoglobin DNA C A C G T A G A C T G A G G A C A C…

Sickle cell hemoglobin mRNA

Sickle cell hemoglobin AA sequence

4. What type of mutation is this? Please explain why.

----------------------------------------------------------------------------------------------------------------------------- -------------------------------

You might also like