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If a strand of DNA with the sequence TGA mutated to GCA would it be a silent or missense mutation?
Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will.
Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.
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A molecule of mRNA with the sequence GGUCAUCACUAU experienced a point mutation that caused the sequence to become GGUUAUCACUAU. Which of the following terms describes this type of mutation?
The mutation described is a "silent mutation." This term is used because the change from G to U in the second position of the sequence does not alter the resulting amino acid due to the redundancy in the genetic code. Specifically, both GGU and GGU (the original and mutated sequences) code for the same amino acid, glycine. Therefore, the mutation does not affect the protein's sequence or function.
What change to this sequence would indicate a silent mutation?
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
What is a A genetic mutation that does not result in a change in the amino acid sequence of the resulting protein is called?
a silent mutation.
What does codon mutation mean?
A codon mutation refers to a change in the sequence of nucleotides in a codon, which is a three-nucleotide segment of DNA or RNA that codes for a specific amino acid. This mutation can lead to various outcomes, such as a silent mutation (no change in the amino acid), a missense mutation (change in one amino acid), or a nonsense mutation (premature stop codon). The effects of codon mutations on protein function can vary significantly, potentially leading to diseases or altered traits.
Will the protein coded by the mutated strand of DNA function differently from the original strand?
It depends on the particular mutation. Some are "silent" which means the substitution of a base actually codes for the same amino acid as the previous. In this case, the sequence and function of the polypeptide is exactly the same. If the mutation is a nonsense or missense mutation however, then the structure and function of the protein is indeed affected. A nonsense mutation results in a codon becoming a "stop" codon, thereby terminating the polypeptide prematurely. Such proteins are nonfunctional. Missense mutations result in the change in sequence of amino acids; one amino acid takes the place of another due to the changed codon. These proteins can also be non-functional, but sometimes they can function, albeit less efficiently.
Which type of mutation results in abnormal acid sequence?
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
A molecule of mRNA with the sequence GGUCAUCACUAU experienced a point mutation that caused the sequence to become GGUUAUCACUAU. Which of the following terms describes this type of mutation?
The mutation described is a "silent mutation." This term is used because the change from G to U in the second position of the sequence does not alter the resulting amino acid due to the redundancy in the genetic code. Specifically, both GGU and GGU (the original and mutated sequences) code for the same amino acid, glycine. Therefore, the mutation does not affect the protein's sequence or function.
What One example of a mutation that would not affect an organisms phenotype?
A silent mutation is an example of a mutation that would not affect an organism's phenotype. This type of mutation occurs in a non-coding region of DNA, such as an intron, and does not change the amino acid sequence of the protein produced. Therefore, it has no impact on the organism's outward appearance or characteristics.
What change to this sequence would indicate a silent mutation?
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
What is a A genetic mutation that does not result in a change in the amino acid sequence of the resulting protein is called?
a silent mutation.
What does codon mutation mean?
A codon mutation refers to a change in the sequence of nucleotides in a codon, which is a three-nucleotide segment of DNA or RNA that codes for a specific amino acid. This mutation can lead to various outcomes, such as a silent mutation (no change in the amino acid), a missense mutation (change in one amino acid), or a nonsense mutation (premature stop codon). The effects of codon mutations on protein function can vary significantly, potentially leading to diseases or altered traits.
Will the protein coded by the mutated strand of DNA function differently from the original strand?
It depends on the particular mutation. Some are "silent" which means the substitution of a base actually codes for the same amino acid as the previous. In this case, the sequence and function of the polypeptide is exactly the same. If the mutation is a nonsense or missense mutation however, then the structure and function of the protein is indeed affected. A nonsense mutation results in a codon becoming a "stop" codon, thereby terminating the polypeptide prematurely. Such proteins are nonfunctional. Missense mutations result in the change in sequence of amino acids; one amino acid takes the place of another due to the changed codon. These proteins can also be non-functional, but sometimes they can function, albeit less efficiently.
What happens during a substitution mutation and how does it impact the genetic code?
During a substitution mutation, a single nucleotide in the DNA sequence is replaced with a different nucleotide. This can lead to a change in the amino acid that is coded for, potentially altering the protein that is produced. The impact on the genetic code depends on whether the substitution results in a silent mutation (no change in the amino acid) or a missense mutation (change in the amino acid), which can affect the function of the protein.
What kind of mutation results from substitution from one nitrogen base to another?
A substitution mutation occurs when one nitrogen base in the DNA sequence is replaced by another. This can lead to three possible outcomes: it may result in a silent mutation (no change in the amino acid), a missense mutation (a different amino acid is produced), or a nonsense mutation (a premature stop codon is introduced). The specific effect depends on the location and nature of the substitution within the genetic code.
Which type of mutation would only affect one amino acidwhich type of mutation would only affect one amino acid?
A missense mutation is the type that would only affect one amino acid in a protein sequence. This occurs when a single nucleotide change in the DNA sequence results in the substitution of one amino acid for another in the corresponding protein. This alteration can potentially impact the protein's function, depending on the role of the altered amino acid. Other mutations, like silent or nonsense mutations, do not affect the amino acid sequence in the same way.
What codes for the same silent point mutation?
A silent point mutation is a change in a DNA sequence that does not alter the amino acid sequence of the resulting protein. This often occurs due to the redundancy of the genetic code, where multiple codons can code for the same amino acid. For instance, both GAA and GAG codons code for glutamic acid, so a mutation from GAA to GAG would be a silent mutation. Thus, any codon that codes for the same amino acid as the original codon can be considered as coding for the same silent point mutation.
A mutation that occurs at a specific location within a nucleotide sequence is called a?
Point mutation and it can be effective or silent depend upon at the site of codon
