To understand what causes a frameshift mutation, we need to first understand what a frameshift mutation is.
A frameshift mutation is a type of genetic mutation wherein a number of nucleotides that is not a multiple of three are inserted or deleted from a DNA sequence. Because the genetic code is read in groups of three nucleotides, called codons, any addition or deletion that does not occur in multiples of three will disrupt the reading frame. This results in a completely different translation from the original.
In the given options, the potential causes for frameshift mutations are:
From the options, Acridine is the correct answer as it causes frameshift mutations by intercalating into DNA and disrupting the base-pairing, leading to insertions or deletions.
Thus, the correct answer is:
| Correct Answer: | Acridine |
Identify the taxa that constitute a paraphyletic group in the given phylogenetic tree.
The vector, shown in the figure, has promoter and RBS sequences in the 300 bp region between the restriction sites for enzymes X and Y. There are no other sites for X and Y in the vector. The promoter is directed towards the Y site. The insert containing only an ORF provides 3 fragments after digestion with both enzymes X and Y. The ORF is cloned in the correct orientation in the vector using the single restriction enzyme Y. The size of the largest fragment of the recombinant plasmid expressing the ORF upon digestion with enzyme X is ........... bp. (answer in integer) 