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What else can I help you with?
Was the sequence a result of point or frame shift mutation?
No
What are two types of frame shift mutations?
"I believe there is insertion and deletion, (one kind), and substitutions. (the second kind)" This answer is incorrect, the two types of frameshift mutation are insertion and deletion, these both alter the translation reading frame. A substitution point mutation in DNA is referred to as a single-nucleotide polymorphism and does not result in any change to the translational reading frame. insections and deletions are two types of frameshift mutations
What is never a frameshift mutation?
A point mutation is never a frameshift mutation because it involves the substitution of a single nucleotide for another rather than the insertion or deletion of nucleotides that would disrupt the reading frame of a gene.
How many nucleotides would cause a frame shift mutation?
Adding or subtracting just one nucleotide would cause a frame shift mutation.
What might occur if there was an extra nitrogen base in the middle of the mRNA code?
If there was an extra nitrogen base in the middle of the mRNA code, it could lead to a frameshift mutation during translation. This might cause a shift in the reading frame and result in the production of incorrect or nonfunctional proteins. Ultimately, this could disrupt the normal cellular functions and lead to genetic disorders.
Was the sequence a result of point or frame shift mutation?
No
What is the type of mutation that shifts the reading frame of the genetic message by inserting or deleting a nucleotide?
A frame-shift mutation.
What do point mutations and frame shift mutations have in common?
Point mutations and frame shift mutations both involve changes in the DNA sequence of a gene. However, point mutations result from the substitution of a single nucleotide, while frame shift mutations occur from insertions or deletions of nucleotides, leading to a shift in the reading frame of the gene. Both types of mutations can have significant effects on the resulting protein sequence and function.
What are two types of frame shift mutations?
"I believe there is insertion and deletion, (one kind), and substitutions. (the second kind)" This answer is incorrect, the two types of frameshift mutation are insertion and deletion, these both alter the translation reading frame. A substitution point mutation in DNA is referred to as a single-nucleotide polymorphism and does not result in any change to the translational reading frame. insections and deletions are two types of frameshift mutations
Causes a shift in the reading codons by one base?
A frameshift mutation is caused by the insertion or deletion of a nucleotide in the DNA sequence, leading to a change in the reading frame of codons. This can result in a completely different protein being produced from the altered sequence, affecting the functionality of the protein.
Does frame shift mutation affect hemophilia?
Frame shift mutations that occur on the X chromosome and within the potion of code that controls the formation of clotting factors can cause hemophilia. Frame shift mutations are only one of many types of mutations that can cause the disorder. For hemophilia it's not so much the type of mutation but the location of the mutation within the genetic code.
How can i describe the effects of a frame-shift mutation?
A frame-shift mutation occurs when nucleotides are added or deleted from a DNA sequence, altering the reading frame of the genetic code. This shift can lead to the production of an entirely different and often nonfunctional protein, as the sequence of amino acids is changed downstream of the mutation. Consequently, frame-shift mutations can result in significant biological consequences, including diseases or developmental disorders, depending on the protein affected. Overall, they disrupt normal cellular function by producing abnormal proteins or prematurely truncating them.
What is never a frameshift mutation?
A point mutation is never a frameshift mutation because it involves the substitution of a single nucleotide for another rather than the insertion or deletion of nucleotides that would disrupt the reading frame of a gene.
What gene has the base sequence CGT AT what the frame shift mutation?
A frameshift mutation occurs when there is an insertion or deletion of nucleotides in a DNA sequence that alters the reading frame of the gene. In the sequence you provided, "CGT AT," if either an additional nucleotide is inserted or one is deleted, it would shift the reading frame, potentially resulting in a completely different and dysfunctional protein being produced. To specifically identify the gene or its function, additional context or the complete sequence would be necessary.
Why are insertions and deletions called frame shift mutations?
Insertions and deletions are called frame shift mutations because they alter the reading frame of the genetic code during protein synthesis. When nucleotides are added or removed in numbers that are not multiples of three, the triplet codons shift, leading to a completely different sequence of amino acids downstream from the mutation. This can result in nonfunctional proteins or significantly altered functions, as the original codon sequence is disrupted.
What is frame shift?
A frame shift mutation is one in which the "reading frame" for protein synthesis is altered. Starting from the DNA, you have either the insertion or deletion of one or more base pairs (but not in a multiple of three). For example, onebase pairmay be inserted into the coding portion of a gene. This is transcribed into mRNA then taken to the ribosome to be "read" (translated) by the tRNA. However, tRNA has three bases on the end of it, which correspond to a specific amino acid. By adding one base into the sequence, you "shift" the reading frame by one base pair and completely change the entire remaining amino acid sequence. Note that if you were to add or subtract three (or a multiple of three) base pairs, you would not shift the frame - you would add or subtract amino acids, but the remaining ones would be the same as the original sequence.
How many nucleotides would cause a frame shift mutation?
Adding or subtracting just one nucleotide would cause a frame shift mutation.
