A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is a silent mutation. a missense mutation. a nonsense mutation. a frameshift mutation. both b and c.

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Answer 1

Textbook Question

Chapter 13, Problem 1TY

A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is

a silent mutation.
a missense mutation.
a nonsense mutation.
a frameshift mutation.
both b and c.

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

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Answer 2

Textbook Question

Chapter 13, Problem 1TY

A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is

a silent mutation.
a missense mutation.
a nonsense mutation.
a frameshift mutation.
both b and c.

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

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Answer 3

Textbook Question

Chapter 13, Problem 1TY

A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is

a silent mutation.
a missense mutation.
a nonsense mutation.
a frameshift mutation.
both b and c.

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

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Answer 4

Textbook Question

Chapter 13, Problem 1TY

A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is

a silent mutation.
a missense mutation.
a nonsense mutation.
a frameshift mutation.
both b and c.

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

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Answer 5

Textbook Question

Answer 6

Textbook Question

Answer 7

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

Answer 8

Expert Solution & Answer

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer to Problem 1TY

Option (d).

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Summary Introduction

Introduction:

The mutation can be described as a condition in which the nucleotide sequence of the DNA is altered. Even a single change in nucleotide may result in many consequences.

Answer 12

Answer to Problem 1TY

Option (d).

Answer 13

Explanation of Solution

Explanation for Correct Answer:

Option (d) frameshift mutation. The frameshift mutation occurs due to a deletion or insertion of nucleotide, which is not a multiple of 3. It causes the shifting of the entire reading frame of DNA sequence, which is the reason it is named so. Sometimes, frameshift mutation may cause deletion of a nucleotide and resulting in a premature presence of stop codon and terminate the sequence prior resulting in short polypeptide or inactivation of the gene product. Hence, it is the correct answer.

Explanation for the incorrect answer:

Option (a) silent mutation. The silent mutation results in the change of nucleotide but does not affect the amino acid or protein formed by that. Hence, it is an incorrect answer.

Option (b) missense mutation. The missense mutation is a mutation that results in the change of nucleotide and replaces the amino acid in the protein sequence, but the length of the sequence remains unaffected. Hence, it is an incorrect answer.

Option (c) nonsense mutation. The non-sense mutations can be described as point mutation which results in the occurrence of a premature stop codon due to the replacement of a nucleotide. In this mutation, the presence of stop codon before the end of the sequence result in early termination of the amino acid formation and result in shorter polypeptide. Hence, it is an incorrect answer.

Option (e) both (b) and (c). As both the option (b) and (c)are incorrect answers, this is also an incorrect option.

Answer 14

Ch. 13.1 - Prob. 1CC Ch. 13.1 - Prob. 2CC Ch. 13.1 - Prob. 1TYK Ch. 13.1 - Prob. 2TYK Ch. 13.2 - Prob. 1CC Ch. 13.2 - Prob. 2CC Ch. 13.2 - Prob. 1TYK Ch. 13.2 - Prob. 2TYK Ch. 13.3 - Prob. 1CC Ch. 13.3 - Prob. 1TYK

A mutation removes a single base pair within the coding sequence of a gene and inactivates the protein encoded by the gene. Such a mutation is a silent mutation. a missense mutation. a nonsense mutation. a frameshift mutation. both b and c.

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