0
Want this question answered?
Be notified when an answer is posted
Add your answer:
Earn +20 pts
When a nitrogenous base is inserted or delete how does that affect the amino acid sequence?
The amino acid sequence is shifted, and this kind of mutation is called a frame shift mutation. All of the amino acid sequence after the mutation will be changed, which will cause a change in shape of the protein, which will then probably result in a nonfunctional protein, since the shape of a protein determines its function.
What are the similarities of a nonsense mutation and a missense mutation?
Both nonsense and missense mutations are point mutations - meaning a single base has been substituted. The difference between the two is that a missense mutation results in an amino acid being replaced with a different amino acid, whereas a nonsense mutation results in a premature stop codon.
How can a point mutation alter the final structure of a protein?
In a point mutation, one nitrogen base is substituted for the correct base. Since most amino acids can be coded for by more than one codon, there may be no consequence to this mutation. However, sometimes a point mutation results in an incorrect amino acid being added to the amino acid sequence of the protein. This can cause a change in the shape and therefore function of the protein, which can be a harmful mutation. Two genetic disorders caused by a point mutation are cystic fibrosis and sickle cell anemia.
Why can a mutation affect the function of protein?
Because a protein's function is dependent on is shape, and a mutation may change the composition (the sequence of amino acids) of a protein, which may in turn cause the shape of the molecule to change.
What is the difference between a point mutation and an insertion and deletion?
Because a point mutation is the replacement of a single base with another base. Thus, if the replacement base codes for the same type amino acid, such as a hydrophobic type amino acid replacing a hydrophobic amino acid, no change to the protein coded for will occur. If a deletion mutation occurs then the code for the protein is disrupted and the protein product is probably going to be useless to the body and may even cause a disease.
What mutation can change every amino acid that follows the point of mutation?
Frameshift mutations MAY change every amino acid that follows the point of mutation.
What One example of a mutation that would not affect an organisms phenotype?
A Missense Mutation.It is a point mutation where the mutations alters the base sequence without changing the resulting function of the subsequent protein. This is usually when the mutation does not change the amino acid which the codon codes for.
What is a synonymous polymorphism?
A synonymous polymorphism is where a mutation alters the base in the DNA sequence but doesn't alter the amino acid encoded (due to the redundancy of the genetic code). Typically, for it to be classified as a polymorphism (as opposed to a mutation) it must occur in greater than 1% of the population.
What is a genetic mutation that does not result in a change in the amino acid sequence of the resulting protein?
It is neutral mutation. Codons are made up of 3 base pairs. This gives 64 different combinations, but there are only 20 amino acids, so some different codons will code for the same amino acid. When the base pair that is changed doesn't cause a change in the amino acid it codes for, then ultimately nothing happens
When a nitrogenous base is inserted or delete how does that affect the amino acid sequence?
The amino acid sequence is shifted, and this kind of mutation is called a frame shift mutation. All of the amino acid sequence after the mutation will be changed, which will cause a change in shape of the protein, which will then probably result in a nonfunctional protein, since the shape of a protein determines its function.
What type of mutation causes protein to be synthesized with one incorrect amino acid?
Missense
What is a change in nucleotide-base sequence of a gene or DNA molecule?
A change in a nucleotide base sequence is known as a point mutation, this is when one of the bases(A,T,C,G) is swapped with another. This causes for the amino acid to change, which can change the function of the amino acid chain.
What are the similarities of a nonsense mutation and a missense mutation?
Both nonsense and missense mutations are point mutations - meaning a single base has been substituted. The difference between the two is that a missense mutation results in an amino acid being replaced with a different amino acid, whereas a nonsense mutation results in a premature stop codon.
How can a point mutation alter the final structure of a protein?
In a point mutation, one nitrogen base is substituted for the correct base. Since most amino acids can be coded for by more than one codon, there may be no consequence to this mutation. However, sometimes a point mutation results in an incorrect amino acid being added to the amino acid sequence of the protein. This can cause a change in the shape and therefore function of the protein, which can be a harmful mutation. Two genetic disorders caused by a point mutation are cystic fibrosis and sickle cell anemia.
How many amino acids are affected from point mutation?
A point mutation can affect the protein in a different ways. If the point change causes a silent mutation then it doesnt affect at all. When the point nucleotide change make a different amino acid, then it may alters the function of protein. If it make to forma a stop codon (TAA, TAG, TGA) then the protein synthesis stops at the point where it is changed.
Why frameshift mutations have greater effect than point mutations?
A substitution mutation means that one base was copied incorrectly within a string of DNA. Since it takes three DNA bases to code for a single amino acid, only one amino acid is affected. A frameshift mutation, on the other hand, refers to an insertion or deletion of any number of DNA bases NOT divisible by three. This mutation throws off EVERY other amino acid after it and tends to be devastating. For example, if you had this sequence: actgactga, you would get three amino acids: act, gac, and tga. If you had a substitution error, it might yield cctgactga. In this case, only the first acid would be different. In the case of an insertion (one type of frameshift mutation), you might get: acttgactga. As you can see, a t-base has been added towards the beginning. in this case, you would get the amino acid sequence: act, tga, ctg. EVERY amino acid following the mutation is different from what it should be.
When is a single base substitution mutation least likely to be deleterious?
when the single base change results in a codon that specifies the same amino acid as the original codon
