Mutation Practice, Exercises of Genetics

1. Following the same procedure you followed during the decoding activity (DNA to mRNA to. Amino Acid), decode the original and mutated sequences and identify ...

Typology: Exercises

2022/2023

Uploaded on 02/28/2023

yorket
yorket 🇺🇸

4.4

(38)

276 documents

1 / 3

Toggle sidebar

This page cannot be seen from the preview

Don't miss anything!

bg1
Name: ___________________________________________ Date: __________________ Period: _____
Code Cracking
Mutation Practice
Review:
Three of the most common types of mutations are:
1. POINT MUTATION (one base is substituted for another)
If a point mutation changes the amino acid, it’s called a MISSENSE mutation.
If a point mutation does not change the amino acid, it’s called a SILENT mutation.
If a point mutation changes the amino acid to a “stop,” it’s called a NONSENSE mutation.
2. INSERTION (an extra base, or bases, is inserted)
3. DELETION (a base, or bases, is lost)
Deletion and insertion may cause what’s called a FRAMESHIFT, meaning the reading frame changes.
These are typically one of the most serious types of mutations.
Directions:
1. Following the same procedure you followed during the decoding activity (DNA to mRNA to
Amino Acid), decode the original and mutated sequences and identify them as one of the three
types of mutations listed above. If it is a point mutations, include whether it is a missense, silent,
or nonsense mutations.
The original DNA sequence is:
DNA: TGC GTG CTT AAG CGG TGT ACA CGT TGC
mRNA:
Amino acid:
Symbol:
pf3

Partial preview of the text

Download Mutation Practice and more Exercises Genetics in PDF only on Docsity!

Name: ___________________________________________ Date: __________________ Period: _____

Code Cracking

Mutation Practice

Review: Three of the most common types of mutations are:

  1. POINT MUTATION (one base is substituted for another)

If a point mutation changes the amino acid, it’s called a MISSENSE mutation. If a point mutation does not change the amino acid, it’s called a SILENT mutation. If a point mutation changes the amino acid to a “stop,” it’s called a NONSENSE mutation.

  1. INSERTION (an extra base, or bases, is inserted)
  2. DELETION (a base, or bases, is lost)

Deletion and insertion may cause what’s called a FRAMESHIFT , meaning the reading frame changes. These are typically one of the most serious types of mutations.

Directions:

  1. Following the same procedure you followed during the decoding activity (DNA to mRNA to Amino Acid), decode the original and mutated sequences and identify them as one of the three types of mutations listed above. If it is a point mutations, include whether it is a missense, silent, or nonsense mutations.

The original DNA sequence is:

DNA: TGC GTG CTT AAG CGG TGT ACA CGT TGC

mRNA:

Amino acid:

Symbol:

Now decode the following mutated sequences:

2. TGC GTG CTT AAG CGA TGT ACA CGT TGC

What kind of mutation is this?

Do you think it will affect the protein’s function? Why?

3. TGC GTG CTT AAG CGG TGT GCA CGT TGC

What kind of mutation is this?

Do you think it will affect the protein’s function? Why?

4. TGC GTG CTT AAG TAG TGT ACA CGT TGC

What kind of mutation is this?

Do you think it will affect the protein’s function? Why?

5. TGC GTG CTT ACT CGG TGT GCA CGT TGC

What kind of mutation is this?

Do you think it will affect the protein’s function? Why?