Which mutation point or frameshift would probably have the greatest effect on the protein?

Answer and Explanation: The type of mutation that is likely to have the greatest effect on a protein is B. Nonsense mutation

Nonsense mutation

In genetics, a nonsense mutation is a point mutation in a sequence of DNA that results in a premature stop codon, or a nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and usually nonfunctional protein product.

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Nonsense mutation - Wikipedia

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Which point mutation has the greatest effect?

At the short end of the spectrum, indels of one or two base pairs within coding sequences have the greatest effect, because they will inevitably cause a frameshift (only the addition of one or more three-base-pair codons will keep a protein approximately intact).

Which has a more serious effect 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.

Which type of mutation point or frameshift do you think is most likely to have the greatest impact on the final polypeptide sequence?

Frameshift mutations have a more dramatic effect on the polypeptide than missense or nonsense mutations. Instead of just changing one amino acid, frameshifts cause a change in all the amino acids in the rest of the gene.

Why is frameshift the most harmful mutation?

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.

Mutations (Updated)

Why does a frameshift have a greater effect on protein structure?

Due to the triplet nature of codons, the amino acid sequence of a protein is determined by contiguous triplets. Therefore, a frameshift mutation leads to completely different proteins in term of chemical composition, and the closer to 5′ end of coding sequence the mutation occurs, the more protein changes it can make.

Is insertion or deletion more harmful?

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.

Which type of mutation will probably have the most serious effect on an individual Why?

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.

Which type of mutation is most likely to cause a change in a protein's structure and function?

Answer and Explanation: A frameshift mutation is one that will most likely cause a change in the protein's structure and function. This is because frameshift mutations...

Why are frameshift mutations so destructive to proteins?

If a mutation disrupts this normal reading frame, then the entire gene sequence following the mutation will be incorrectly read. This can result in the addition of the wrong amino acids to the protein and/or the creation of a codon that stops the protein from growing longer.

Which mutation is most harmful?

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.

Which type of mutations can result in a frameshift?

Insertions, deletions, and duplications can all be frameshift variants. Some regions of DNA contain short sequences of nucleotides that are repeated a number of times in a row.

Does frameshift mutation affect protein?

Hence, frameshift mutations result in an abnormal or defective protein product containing an improper sequence of amino acids. Depending upon the location of the mutation, such proteins may be wholly new or non-usable. Frameshift mutation can also result in the stop codon.

Which of these mutations is likely to have the most serious effect on the protein?

The most serious of these mutations will be the insertion of 2 bases. Becasue the genetic code is read in triplets, a 2 base insetion will alter the reading frame of the code causing a frameshift mutation meaning every amino acid after the site of the mutation will be incorrect.

Why is a frameshift missense mutation more likely to have a severe effect on phenotype than a nucleotide pair substitution missense mutation in the same protein?

Why is a frameshift missense mutation more likely to have a severe effect on phenotype than a nucleotide-pair substitution missense mutation in the same protein? A substitution missense affects only one codon, but a frameshift missense affects all codons downstream of the frameshift.

Which mutation is least likely to cause a frame shift?

So, the correct option is 'A missense substitution'

What type of gene mutation is least likely to cause a change in protein structure?

Silent mutations are least likely to affect protein function.

Which mutation 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.

Which of the following mutations is likely to have the most severe impact on gene expression?

Which of the following gene mutations is most likely to have the most severe impact on gene expression? c. a point mutation in the splice-donor site of an intron. A point mutation in the splice-donor site of an intron would result in the intron sequence inappropriately remaining in the mRNA.

Which mutation is the least harmful?

The majority of mutations have neither negative nor positive effects on the organism in which they occur. These mutations are called neutral mutations. Examples include silent point mutations. They are neutral because they do not change the amino acids in the proteins they encode.

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 nonsense mutation worse than frameshift mutation?

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 mutation is potentially more harmful or causes greater consequence?

Because germ-line mutations affect the entire organism, they are potentially more harmful (or beneficial), but this is not always the case. Somatic mutations can cause quite harmful effects such as cancer. 8.

What is the difference between frameshift mutation and point mutation?

What is the difference between frameshift mutation and point mutation? In a frameshift mutation, deletion or insertion of one nucleotide leads to change in the reading frame of codons in a gene from that point onwards, whereas in point mutation, there is a change in only one base pair of DNA due to substitution.

How does a frameshift mutation affect protein function quizlet?

How does a frameshift mutation affect protein function? a. Protein function is most likely inhibited because an entirely new amino acid sequence occurs downstream of the mutation.