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In the DNA, the sequence of nucleotides determines how proteins are built, with each segment of three nucleotides encoding a single amino acid. When one nucleotide is inserted into the sequence, the whole sequence shifts, and all the triples are changed completely, which can cause detrimental mutations.
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Why does an insertion mutation usually cause more defects in protein synthesis than a point mutation?
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
Can a point mutation be frameshift mutation?
No
During DNA replication an extra cytosine base is added to the DNA what type of mutation is this?
A frameshift mutation
Why does an insertion mutation usually cause defects during protein synthesis than a point mutation?
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
Adding an extra nucleotide to a DNA sequence producers what type of mutation?
Insertion
Why does an insertion mutation usually cause more defects in protein synthesis than a point mutation?
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
A nucleotide sequence changes from TAGCAT to TAGGCAT. what type of mutation occured?
Insertion?
Can a point mutation be frameshift mutation?
No
During DNA replication an extra cytosine base is added to the DNA what type of mutation is this?
A frameshift mutation
In a certain mutation several nucleotides which weren't there before are put into a sequence This is an example of a?
This is an example of an insertion mutation. Insertion mutations involve the addition of extra nucleotides into a DNA sequence, which can lead to significant changes in the genetic code and potentially disrupt normal gene function.
Is a change in the base sequence of a DNA molecule?
a kind of mutation called deletion or insertion
What is a change in the base sequence of DNA molecule?
a kind of mutation called deletion or insertion
What is the mutation caused by the addition of a nucleotide to an already existing gene sequence called deletion duplication insertion inversionWhat is the mutation caused by the addition of a nucleot?
The mutation caused by the addition of a nucleotide to an existing gene sequence is called an "insertion." This type of mutation can disrupt the reading frame of the gene, potentially leading to significant changes in the resulting protein. If the insertion occurs within a coding region, it can alter the amino acid sequence and affect the protein's function.
Why does an insertion mutation usually cause defects during protein synthesis than a point mutation?
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
Adding an extra nucleotide to a DNA sequence producers what type of mutation?
Insertion
Why does an insertion mutation cause more defects than point mutation?
An insertion mutation adds one or more nucleotides into the DNA sequence, which can disrupt the reading frame of the gene. This frameshift can lead to the production of a completely different and often nonfunctional protein, resulting in significant defects. In contrast, a point mutation typically alters just a single nucleotide, which may only change one amino acid or have no effect at all, making it generally less disruptive than an insertion mutation. Thus, the broader impact of an insertion mutation often leads to more severe consequences in gene function.
What type of mutation is caused by adding one nucleotide into the middle of a sequence?
A frameshift mutation is caused by adding one nucleotide into the middle of a sequence. This type of mutation alters the reading frame of the genetic code, leading to a completely different amino acid sequence downstream of the insertion point.
