Genetic Mutations and Codon Functions

Genetic Mutations and Codon Functions

Assessment

Interactive Video

Biology

9th - 10th Grade

Hard

Created by

Patricia Brown

FREE Resource

The video tutorial explains deletion mutations, specifically frame shift mutations, where a single nucleotide is deleted, altering the reading frame of DNA. It covers how DNA is transcribed into messenger RNA, which is then translated into proteins. The tutorial details the process of base pairing between DNA and RNA, and how codons specify amino acids. It highlights the impact of a deletion mutation on the amino acid sequence, emphasizing the concept of the degenerate code, where multiple codons can code for the same amino acid, affecting the resulting protein's functionality.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a deletion mutation also known as?

Point mutation

Missense mutation

Frame shift mutation

Silent mutation

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which base does adenine pair with in mRNA?

Thymine

Cytosine

Uracil

Guanine

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What amino acid does the mRNA codon AUG code for?

Tyrosine

Alanine

Methionine

Tryptophan

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which amino acid is specified by the mRNA codon UAC?

Alanine

Phenylalanine

Tyrosine

Tryptophan

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does a deletion mutation affect the reading frame of DNA?

It does not affect the reading frame

It shifts the reading frame

It duplicates the reading frame

It reverses the reading frame

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the result of a shifted reading frame due to a deletion mutation?

No change in protein function

A completely different amino acid sequence

A longer protein

A shorter protein

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why does the third amino acid remain the same despite a codon change?

Because of a missense mutation

Because of the degenerate code

Because of a nonsense mutation

Because of a silent mutation

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