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Which Of The Following Dna Mutations Is Most Likely To Damage The Protein It Specifies? Trust The Answer

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Which Of The Following Dna Mutations Is Most Likely To Damage The Protein It Specifies?
Which Of The Following Dna Mutations Is Most Likely To Damage The Protein It Specifies?

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Which type of mutation is most damaging to the protein?

Insertion or deletion, which leads to frameshift mutation is more damaging. It causes changes in the subsequent amino acid sequences in a polypeptide chain.

Which DNA mutation is most damaging?

Deletion mutations, on the other hand, are opposite types of point mutations. They involve the removal of a base pair. Both of these mutations lead to the creation of the most dangerous type of point mutations of them all: the frameshift mutation.


The different types of mutations | Biomolecules | MCAT | Khan Academy

The different types of mutations | Biomolecules | MCAT | Khan Academy
The different types of mutations | Biomolecules | MCAT | Khan Academy

Images related to the topicThe different types of mutations | Biomolecules | MCAT | Khan Academy

The Different Types Of Mutations | Biomolecules | Mcat | Khan Academy
The Different Types Of Mutations | Biomolecules | Mcat | Khan Academy

Which of the following types of mutations is most likely to disrupt a protein’s function?

Nonsense and frameshift mutations would be most likely to disrupt protein function. A nonsense mutation would cause the protein to be much shorter and a frameshift mutation would alter the amino acid sequence downstream from the mutation.

Which type of mutation of DNA would have the greatest effect on proteins that result from translation?

Frameshift mutations

The outcome of a frameshift mutation is complete alteration of the amino acid sequence of a protein. This alteration occurs during translation because ribosomes read the mRNA strand in terms of codons, or groups of three nucleotides.

Which is more harmful point or frameshift mutation?

Frameshift mutations are generally much more serious and often more deadly than point mutations. Even though only a single nitrogen base is affected, as with point mutations, in this instance, the single base is either completely deleted or an extra one is inserted into the middle of the DNA sequence.

Why are insertion and deletion mutations so harmful?

Because an insertion or deletion results in a frame-shift that changes the reading of subsequent codons and, therefore, alters the entire amino acid sequence that follows the mutation, insertions and deletions are usually more harmful than a substitution in which only a single amino acid is altered.

Which mutation is worse insertion or deletion?

In case of deletion or insertion of a particular fragment of the gene, deletion could be more harmful than insertion, because the deleted fragment of the gene will never be replaced at exact size and exact position of the disabled gene.


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Biology chapter 14 Flashcards | Quizlet

Which of the following DNA mutations is most likely to damage the protein it specifies? a base-pair deletion.

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DNA Mutation and Repair – California State University …

Point mutations that occur in DNA sequences encoding proteins are either silent, … base substitution results in the generation of a codon that specifies a …

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Types and Examples of DNA Mutations – ThoughtCo

That messenger RNA codon is then translated into an amino acid that goes on to make a protein that will be expressed by the organism. Depending …

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Which mutation is potentially more harmful or causes greater consequence?

Random mutations are more likely to be harmful than beneficial. The genes within each species have evolved to work properly. They have functional promoters, coding sequences, terminators, and so on, that allow the genes to be expressed.

Which is more harmful nonsense or missense mutations?

Radical missense mutations were found to be four times more deleterious compared to conservative ones. Surprisingly, we found that silent mutations on average are not neutral; with the average harmfulness of 3% of nonsense mutations.

Which type of mutation is least likely to affect protein function?

Silent mutations are least likely to affect protein function. Missense mutations are often difficult to predict. If the change is to a similar amino acid or in a non-critical amino acid, the mutation protein may continue to function.

Which type of mutation is least likely to affect protein function quizlet?

Because they only affect a single amino acid, missense mutations do not have a significant effect on protein functions.

How does frameshift mutation affect the protein?

Frameshift mutations are among the most deleterious changes to the coding sequence of a protein. They are extremely likely to lead to large-scale changes to polypeptide length and chemical composition, resulting in a non-functional protein that often disrupts the biochemical processes of a cell.

Which of the following types of mutation would have the most severe effect?

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.

Why do frameshift mutations have a greater effect?

Also frameshift mutations have a greater effect than point mutations because it throws off the reading frame since codons code for different amino acids. Another point is that frameshift mutations have a greater effect than point mutations because insertion and deletion are stronger than substitution.


Mutations (Updated)

Mutations (Updated)
Mutations (Updated)

Images related to the topicMutations (Updated)

Mutations (Updated)
Mutations (Updated)

What are some examples of harmful mutations?

Harmful mutations may cause genetic disorders or cancer. A genetic disorder is a disease caused by a mutation in one or a few genes. A human example is cystic fibrosis. A mutation in a single gene causes the body to produce thick, sticky mucus that clogs the lungs and blocks ducts in digestive organs.

Is nonsense mutation worse than frameshift?

Frame shift would be the worst as it would change the most. Missense and nonsense change one point along the chain. Which can be detrimental but if it is, it only changes one protein chain.

Which of the mutations would most likely have the least severe consequences?

synonymous (silent) mutation. Which of the mutations would most likely have the least severe consequences? A match between the DNA in a sample and the genomic DNA of a particular individual for a single tandem repeat site is not sufficient to establish identity. However, a mismatch is definitive.

Why is a frameshift mutation is more likely to result in a nonfunctional protein?

A frameshift variant occurs when there is an addition or loss of nucleotides that shifts the grouping and changes the code for all downstream amino acids. The resulting protein is usually nonfunctional. Insertions, deletions, and duplications can all be frameshift variants.

Why are insertion and deletion mutations so harmful quizlet?

Why are insertion and deletion (frameshift) mutations so harmful? They change all of the codons from the mutation on down the line, which changes the amino acid sequence ultimately changing the protein.

Are all types of mutation harmful?

Most mutations are not harmful, but some can be. A harmful mutation can result in a genetic disorder or even cancer. Another kind of mutation is a chromosomal mutation. Chromosomes, located in the cell nucleus, are tiny threadlike structures that carry genes.

What are insertion deletion and substitution mutations?

Substitution mutations are mutations in which a base pair is replaced by a different base pair. Insertion mutations are mutations in which one or more nucleotides are added into the DNA sequence. Deletion mutations are mutations in which one or more nucleotides are removed from the DNA sequence.

Is frameshift mutation harmful?

Frameshift mutation yields truncated, dysfunctional product proteins, leading to loss-of-function, genetic disorders or even death. Frameshift mutations have been considered as mostly harmful and of little importance for the molecular evolution of proteins.

Is a point mutation always damaging?

General consequences. Point mutations that occur in non-coding sequences are most often without consequences, although there are exceptions. If the mutated base pair is in the promoter sequence of a gene, then the expression of the gene may change.

Why is substitution the least harmful mutation?

Substitution Mutations

A substitution mutation is when one nucleotide is swapped out for another. These types of mutations are the least dangerous of all the DNA mutations. That’s because a single nucleotide change does not usually have a very large effect on the final protein.

Which type of mutation is least likely to affect protein function?

Silent mutations are least likely to affect protein function. Missense mutations are often difficult to predict. If the change is to a similar amino acid or in a non-critical amino acid, the mutation protein may continue to function.

Which type of mutation has the least effect on the protein?

Silent mutation: Some mutations that change DNA bases do not have any effect on the sequence of amino acids in the protein. These mutations are called silent mutations and they do not affect the structure or function of the protein because there is no effect on the amino acid sequence.


Types of DNA mutations and their affect on protein

Types of DNA mutations and their affect on protein
Types of DNA mutations and their affect on protein

Images related to the topicTypes of DNA mutations and their affect on protein

Types Of Dna Mutations And Their Affect On Protein
Types Of Dna Mutations And Their Affect On Protein

Which mutation would have the least effect on the protein?

Explanation: If a mutation does not alter the amino acid sequence of a protein, it is considered a silent mutation. A neutral mutation changes the amino acid, but not the function of the protein. Both frameshift and nonsense mutations can severely affect the function and structure of a protein.

What type of mutation does not alter the protein production?

Silent mutations are when the mutation doesn’t actually affect the protein at all. Since many different RNA codons can code for the same amino acid, it’s possible that the mutation might not affect the protein at all.

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